PHARMA STUFF

Author: Sudheer vanguri

  • Stedman Pharmaceuticals Recruitment: Multiple Vacancies

    Stedman Pharmaceuticals Pvt. Ltd. is inviting applications from qualified candidates for multiple pharmaceutical and corporate job openings.
    The company is hiring for Production, Research & Development, Quality Assurance, Regulatory Affairs, Logistics, Engineering Purchase, Training and Commercial Operations.
    Candidates with qualifications including B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com, M.Com, MBA, BBA, B.E., ITI, Diploma and 12th pass can apply for suitable positions.
    Job locations include Chennai – Taramani and Chennai – Alathur, with opportunities for both experienced professionals and eligible freshers.

    Company Overview

    Stedman Pharmaceuticals Pvt. Ltd. is a pharmaceutical company focused on quality, innovation and healthcare. The company is looking for talented candidates to join its teams across manufacturing, quality, research, logistics, procurement, regulatory affairs and training functions.

    Stedman Pharmaceuticals Job Vacancies

    The company has announced openings across several departments. Candidates should review the qualification and experience requirements for each position before applying.

    1. Manager – Commercial Operations

    • Department: Logistics

    • Qualification: B.Com / M.Com / MBA / Any Degree

    • Experience: 8–10 years

    • Key Skills:

      • C&F and distributor management

      • Order-to-dispatch and sales and distribution MIS

      • Inventory monitoring and commercial reconciliation

      • Team handling and analytical skills

    2. Production Chemist

    • Department: Production

    • Qualification: B.Pharm / M.Pharm

    • Experience: 2–5 years

    • Key Skills:

      • Manufacturing and filling operations

      • Secondary packing operations

      • Raw material checking

      • Line clearance

    3. R&D Chemist

    • Department: Research & Development

    • Qualification: B.Pharm / M.Pharm

    • Experience: 2–4 years

    • Key Skills:

      • Formulation development and laboratory trials

      • Pre-formulation and API-excipient studies

      • Documentation and technology transfer

    4. QA Chemist – IPQA

    • Department: Quality Assurance

    • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

    • Experience: 2–5 years

    • Key Skills:

      • In-process quality checks and line clearance

      • BMR verification and yield reconciliation

      • GMP compliance and product release

    5. QA Chemist – QMS

    • Department: Quality Assurance

    • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

    • Experience: 5–8 years

    • Key Skills:

      • Deviation management

      • CAPA and change control

      • Internal audits and documentation

      • SOPs, APQR and QMS compliance

    6. Junior Executive – Logistics

    • Department: Logistics

    • Qualification: MBA / BBA / Logistics

    • Experience: 2–4 years

    • Key Skills:

      • C&F and distributor management

      • Order-to-dispatch and MIS

      • Inventory and commercial reconciliation

      • MS Excel, ERP, tally and team handling

    7. Junior Executive – Engineering Purchase

    • Department: Purchase & Procurement

    • Qualification: B.E. / MBA

    • Experience: 1–3 years

    • Key Skills:

      • Vendor development and strategic sourcing

      • Purchase order and delivery management

      • CAPEX / AMC / CMC procurement

    8. Junior Executive – Regulatory Affairs

    • Department: Regulatory Affairs

    • Qualification: M.Pharm / M.Sc

    • Experience: 1–3 years

    • Key Skills:

      • Dossier preparation and regulatory filings

      • cGMP documentation and compliance

      • Coordination with global teams

    9. AM – Training

    • Department: Training

    • Qualification: UG / PG in a science background

    • Experience: 10–15 years

    • Key Skills:

      • Product training and evaluation

      • Presentation and communication

      • Team handling and training programmes

    10. Production Operators

    • Department: Production

    • Qualification: ITI / Diploma / 12th

    • Experience: Freshers / 1–3 years

    • Key Skills:

      • Machine operation and GMP

      • Production processes

      • Teamwork

    Eligibility & Qualifications

    Candidates with the following qualifications can apply for relevant openings, depending on the position:

    B.Pharm | M.Pharm | B.Sc | M.Sc | B.Com | M.Com | MBA | BBA | B.E. | ITI | Diploma | 12th Pass

    Applicants should check the individual position requirements for the required educational background and work experience.

    Location & Salary

    Job Locations:

    • Chennai – Taramani

    • Chennai – Alathur

    Salary details have not been specified in the recruitment announcement. Compensation may vary according to the position, qualifications and relevant experience.

    How to Apply

    Interested candidates should prepare their updated resumes and apply by emailing the recruitment team at either of the following addresses:

    Applicants should mention the position they are applying for in their email subject line and include relevant details about their qualifications and experience.

    Important Instructions

    • Review the qualification and experience requirements for the desired position before applying.

    • Candidates should ensure that their resumes include accurate educational and professional details.

    • Freshers may apply for Production Operator positions where the stated experience requirement includes freshers.

    Frequently Asked Questions

    1. Which company is recruiting?

    Stedman Pharmaceuticals Pvt. Ltd. has announced multiple openings across pharmaceutical manufacturing and corporate functions.

    2. Which qualifications are eligible?

    Depending on the position, candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com, M.Com, MBA, BBA, B.E., ITI, Diploma or 12th pass qualifications may apply.

    3. Can freshers apply?

    Yes. The Production Operator vacancy lists freshers and candidates with 1–3 years of experience as eligible.

    4. What experience is required?

    The experience requirement ranges from freshers to 15 years, depending on the position.

    5. Where are the job locations?

    The listed locations are Chennai – Taramani and Chennai – Alathur.

    6. How can candidates apply?

    Candidates can send their updated resumes to hrd@stedmanpharma.com or hrd2@stedmanpharma.com.

    Job Summary

    Category Details
    Company Stedman Pharmaceuticals Pvt. Ltd.
    Vacancies Manager – Commercial Operations; Production Chemist; R&D Chemist; QA Chemist – IPQA; QA Chemist – QMS; Junior Executive – Logistics; Junior Executive – Engineering Purchase; Junior Executive – Regulatory Affairs; AM – Training; Production Operators
    Required Education B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com, M.Com, MBA, BBA, B.E., ITI, Diploma and 12th pass, depending on the role
    Experience Freshers to 15 years, depending on the position

     

  • Fidelity Health Wanted Drug Safety Executive (Case processing and Aggregate Report)

    Fidelity Health Services is hiring for the position of Drug Safety Executive in Ahmedabad, Gujarat. The role focuses on pharmacovigilance case processing, Individual Case Safety Reports (ICSRs), and aggregate safety report preparation. Candidates with M.Pharm, B.Pharm, BAMS, or BHMS qualifications and a minimum of 3–4 years of relevant experience in case processing and aggregate reporting can apply by emailing their updated CV to the recruitment team.

    Company Overview

    Fidelity Health Services operates in the healthcare services sector. This recruitment opportunity is intended for professionals with experience in drug safety operations, pharmacovigilance case processing, safety database management, and aggregate report preparation.

    Job Role & Responsibilities

    Designation: Drug Safety Executive
    Department: Pharmacovigilance / Drug Safety
    Role: Case Processing and Aggregate Reports
    Job Location: Ahmedabad, Gujarat
    Job Type: Full-time, On-site

    Key Responsibilities

    • Enter individual case safety reports into the safety database, including regulatory, literature, spontaneous, and vendor cases.

    • Process serious and non-serious adverse event cases in accordance with applicable procedures.

    • Verify case data against source documents and established procedures.

    • Raise queries to obtain additional information whenever required.

    • Prepare and maintain aggregate report planners to track global reporting timelines.

    • Review and support the preparation of Periodic Adverse Drug Experience Reports (PADER), Periodic Safety Update Reports (PSUR), and Periodic Benefit-Risk Evaluation Reports (PBRER).

    • Collect and consolidate safety data from multiple sources.

    • Maintain aggregate report compliance trackers and monitor reporting requirements.

    • Coordinate with cross-functional teams to ensure that the necessary data is available for aggregate reports.

    • Support corrective and preventive actions (CAPA) related to identified deviations.

    Eligibility / Qualifications

    Candidates must meet the following requirements:

    Educational Qualifications

    • M.Pharm

    • B.Pharm

    • BAMS

    • BHMS

    Experience

    • Minimum 3–4 years of experience in pharmacovigilance case processing and aggregate report preparation.

    Required Skills

    • Practical knowledge of Individual Case Safety Report (ICSR) processing.

    • Experience preparing and reviewing aggregate safety reports.

    • Familiarity with pharmacovigilance systems such as Argus, ArisG, or Veeva.

    • Understanding of safety database management and documentation practices.

    • Knowledge of global pharmacovigilance regulations and compliance requirements, including FDA, EMA, and MHRA standards.

    • Strong analytical, problem-solving, and decision-making skills.

    • Effective communication and cross-functional coordination abilities.

    Location & Salary

    Job Location: Ahmedabad, Gujarat, India
    Work Arrangement: Full-time, on-site

    Application Process

    Eligible candidates can apply by sending their updated CV to the recruitment email address below.

    Frequently Asked Questions

    1. What is the qualification required for the Drug Safety Executive position at Fidelity Health Services?

    Candidates with M.Pharm, B.Pharm, BAMS, or BHMS qualifications are eligible to apply.

    2. Can freshers apply for this pharmacovigilance job?

    No. The recruitment announcement specifies a minimum of 3–4 years of experience in case processing and aggregate report preparation.

    3. What is the job location?

    The position is based in Ahmedabad, Gujarat, and requires on-site work.

    4. What is the expected salary for this position?

    The company has not disclosed the salary. Candidates should confirm compensation details directly with the recruitment team.

    5. How can candidates apply?

    Eligible candidates can email their updated CV to hrrecruitment@fidelityhs.com.

    6. What is the selection process and application deadline?

    The employer has not announced the detailed selection process or application deadline. Shortlisted candidates may receive further instructions from the recruitment team.

    Summary Table

    Company Fidelity Health Services
    Department Vacancies Pharmacovigilance / Drug Safety – Drug Safety Executive
    Qualification M.Pharm, B.Pharm, BAMS, BHMS
    Experience Minimum 3–4 years
    Location Ahmedabad, Gujarat

  • IOL Chemicals Recruitment: API, QA, QC & R&D Jobs

    IOL Chemicals and Pharmaceuticals Limited is conducting a walk-in drive for experienced professionals in API Production, Quality Assurance, Quality Control and Research & Development (R&D / ARD).
    The company is recruiting Chemists and Senior Chemists for its pharmaceutical and chemical manufacturing operations in Panchkula, Haryana.
    Candidates with qualifications in Chemistry, Pharmacy or Chemical Engineering can apply for the relevant positions. Freshers with a Diploma in Chemical Engineering or B.Sc. Chemistry are also eligible for API Production roles.
    The walk-in interview is scheduled for 24 October 2026, from 8:30 AM to 4:00 PM, at Hotel K C Cross Road, Panchkula, Haryana.

    IOL Chemicals and Pharmaceuticals Recruitment: Walk-In Drive

    Company Overview

    IOL Chemicals and Pharmaceuticals Limited is inviting applications from qualified candidates for multiple positions across its API Production, Quality Assurance, Quality Control and Research & Development departments.

    The recruitment drive includes opportunities for experienced professionals as well as freshers interested in API manufacturing.

    Job Openings at IOL Chemicals and Pharmaceuticals Limited

    1. API Production – Chemist / Senior Chemist

    • Qualification: B.Sc. Chemistry / Diploma in Chemical Engineering.

    • Experience: 2–8 years.

    • Freshers: Eligible candidates with a Diploma in Chemical Engineering or B.Sc. Chemistry can apply for API Production roles.

    2. Quality Assurance – Chemist / Senior Chemist

    • Qualification: M.Sc. Chemistry / M.Pharmacy / B.Pharmacy.

    • Experience: 2–8 years.

    3. Quality Control – Chemist / Senior Chemist

    • Qualification: M.Sc. Chemistry / M.Pharmacy.

    • Experience: 2–8 years.

    4. Research & Development (R&D / ARD) – Chemist / Senior Chemist

    • Qualification: M.Sc. Chemistry / M.Pharmacy.

    • Experience: 2–8 years.

    Job Role & Responsibilities

    API Production

    • Support API manufacturing activities and production operations.

    • Follow applicable manufacturing procedures and operational requirements.

    • Maintain relevant production documentation and comply with established safety and quality standards.

    Quality Assurance

    • Support quality assurance activities and applicable documentation.

    • Follow established quality procedures and manufacturing standards.

    • Assist in maintaining compliance with relevant quality requirements.

    Quality Control

    • Support laboratory testing and quality control activities.

    • Follow applicable analytical procedures and documentation practices.

    • Help maintain product quality in accordance with established standards.

    Research & Development / ARD

    • Support research, development and analytical activities relevant to the assigned role.

    • Follow laboratory procedures and maintain appropriate documentation.

    The responsibilities above are general descriptions of the departments. The recruitment announcement does not provide detailed, position-wise job descriptions.

    Eligibility & Qualifications

    Candidates can review the position-wise eligibility requirements below.

    Department Designation Required Qualification Experience
    API Production Chemist / Senior Chemist B.Sc. Chemistry / Diploma in Chemical Engineering 2–8 years
    Quality Assurance Chemist / Senior Chemist M.Sc. Chemistry / M.Pharmacy / B.Pharmacy 2–8 years
    Quality Control Chemist / Senior Chemist M.Sc. Chemistry / M.Pharmacy 2–8 years
    R&D / ARD Chemist / Senior Chemist M.Sc. Chemistry / M.Pharmacy 2–8 years

    Freshers’ eligibility: Freshers with a Diploma in Chemical Engineering or B.Sc. Chemistry are eligible for API Production positions.

    Location & Salary

    Job Location: IOL Chemicals and Pharmaceuticals Limited recruitment drive, Panchkula, Haryana.

    Interview Venue: Hotel K C Cross Road, Site No. 1, Sector 10, opposite the bus stand, Panchkula – 134113, Haryana.

    Salary details have not been specified in the recruitment announcement.

    Walk-In Interview Details

    • Company: IOL Chemicals and Pharmaceuticals Limited

    • Interview Date: Saturday, 24 October 2026

    • Interview Time: 8:30 AM to 4:00 PM

    • Venue: Hotel K C Cross Road, Site No. 1, Sector 10, opposite the bus stand, Panchkula – 134113, Haryana.

    How to Apply

    Eligible candidates can attend the walk-in interview at the specified venue on 24 October 2026.

    Candidates should carry their updated CV or resume, Aadhaar card, educational certificates, salary proofs and one recent passport-size photograph.

    For assistance, candidates can contact the help desk:

    • Contact Number 1: +91 9878996261

    • Contact Number 2: +91 7347027318

    The recruitment poster also provides a QR code for scanning to apply.

    Documents Required

    Candidates should bring the following documents:

    • Updated CV / resume

    • Aadhaar card

    • Educational certificates

    • Salary proofs

    • One recent passport-size photograph

    Important Instructions

    • Candidates should attend the interview during the specified time.

    • Applicants should carry all the documents listed in the recruitment announcement.

    • Freshers may apply for API Production if they hold a Diploma in Chemical Engineering or B.Sc. Chemistry.

    Frequently Asked Questions

    1. Which departments are hiring at IOL Chemicals and Pharmaceuticals Limited?

    The recruitment drive covers API Production, Quality Assurance, Quality Control and R&D / ARD.

    2. What qualifications are required for these vacancies?

    Depending on the department, eligible qualifications include B.Sc. Chemistry, M.Sc. Chemistry, Diploma in Chemical Engineering, B.Pharm and M.Pharm.

    3. Can freshers apply for IOL Chemicals API Production jobs?

    Yes. Freshers with a Diploma in Chemical Engineering or B.Sc. Chemistry are eligible for API Production positions.

    4. How much experience is required?

    The stated experience requirement for the Chemist / Senior Chemist positions is 2–8 years. Freshers are also eligible for the specified API Production openings.

    5. When is the walk-in interview?

    The interview will take place on 24 October 2026, from 8:30 AM to 4:00 PM.

    6. Where is the interview venue?

    The venue is Hotel K C Cross Road, Site No. 1, Sector 10, opposite the bus stand, Panchkula – 134113, Haryana.

    Job Summary

    Category Details
    Company IOL Chemicals and Pharmaceuticals Limited
    Vacancies Chemist / Senior Chemist – API Production, Quality Assurance, Quality Control and R&D / ARD
    Required Education B.Sc. Chemistry / M.Sc. Chemistry / Diploma in Chemical Engineering / B.Pharm / M.Pharm
    Experience 2–8 years for experienced positions; freshers eligible for specified API Production roles

     

  • ICON Plc Wanted Elluminate Programmer (Lead Clinical Data Science Programmer)

    ICON Strategic Solutions is hiring an Elluminate Programmer (Lead Clinical Data Science Programmer) for opportunities in Bangalore and Chennai, India, with remote or office-based work options listed in the recruitment details. Candidates with a Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, Biology, or another health-related field can apply. Applicants should have 3–5 years of programming experience using tools such as Elluminate, Veeva CDB, or JReview, along with hands-on Elluminate report development experience. This opportunity is suited to professionals with clinical data programming, clinical trial reporting, and data cleaning expertise.

    ICON Strategic Solutions Elluminate Programmer Recruitment

    Company Overview

    ICON Strategic Solutions is part of ICON, a global clinical research organisation that supports pharmaceutical, biotechnology, and medical device companies in clinical development. Through its Functional Service Provider (FSP) model, ICON provides dedicated teams and specialist expertise to sponsor organisations.

    This position offers the opportunity to contribute to clinical data solutions that support data quality, clinical trial monitoring, and reporting. The role involves working with cross-functional teams to develop reliable reporting tools and data cleaning solutions for clinical studies.

    Job Details

    • Company: ICON Strategic Solutions (FSP)

    • Designation: Elluminate Programmer / Lead Clinical Data Science Programmer

    • Job Reference: JR157719

    • Job ID: 52885

    • Location: Bangalore and Chennai, India

    • Work Arrangement: Remote or office-based, as listed in the recruitment details

    • Experience: 3–5 years of relevant programming experience

    • Employment Type: Refer to the official job listing

    Job Role & Responsibilities

    The Elluminate Programmer will develop clinical data reporting solutions, create reusable data checks, and support the accurate and timely review of clinical trial data. The position requires collaboration with clinical data management teams, data engineers, configuration specialists, medical reviewers, and other stakeholders.

    Clinical Data Reporting and Programming

    • Develop data cleaning reports, study status metrics, monitoring reports, and visualisations in line with standard and study-specific data review plans.

    • Create and test listings used for clinical data review.

    • Develop reports that support the quality, accuracy, and timely delivery of clinical trial data.

    • Provide programming expertise to support data cleaning and data validation activities.

    • Enhance existing reporting tools, macros, and libraries or develop new solutions for clinical data review and trial status reporting.

    • Contribute to the development of data management reporting standards when required.

    Reusable Checks and Automation

    • Build a library of reusable data checks in collaboration with data engineers and configuration specialists.

    • Work with cross-functional teams to establish business rules and automated checks across TAU.

    • Identify opportunities to improve existing processes and develop innovative concepts for more efficient clinical data review.

    • Support the use of standardised reporting solutions across clinical studies.

    Documentation and Compliance

    • Prepare and maintain documentation for reports and deliverables throughout the study or asset lifecycle.

    • Follow applicable standard operating procedures (SOPs) and established work practices.

    • Ensure data cleaning reports support the relevant data review plan.

    • Work with Clinical Data Management teams and medical reviewers to support operational quality and data integrity.

    Collaboration and Technical Support

    • Serve as a technical resource for developing data analytics that support data validation and cleaning.

    • Help colleagues build knowledge of reporting tools and practices that improve the accuracy and integrity of study data.

    • Collaborate with internal partners to promote operational excellence and consistent reporting practices.

    • Complete assigned tasks independently while meeting agreed deadlines.

    Eligibility & Qualifications

    Educational Qualifications

    Candidates should have one of the following:

    • Bachelor’s degree in Computer Science.

    • Bachelor’s degree in Statistics.

    • Bachelor’s degree in Biostatistics.

    • Bachelor’s degree in Mathematics.

    • Bachelor’s degree in Biology.

    • Bachelor’s degree in another health-related field.

    • Equivalent experience that provides the skills and knowledge needed for the role.

    Experience Requirements

    • 3–5 years of experience in programming listings and/or visualisations using one or more of the following: Veeva CDB, JReview, or Elluminate.

    • Hands-on experience developing reports in Elluminate.

    • Knowledge of the drug development process.

    • Familiarity with clinical trial terminology and clinical database systems.

    Technical Skills

    • Experience with at least one of the following programming or query languages: CQL, SQL, SAS, R, or Python.

    • Understanding of regulatory requirements and relevant clinical data standards.

    • Knowledge of CDISC and SDTM is preferable.

    • Familiarity with clinical database systems such as Metadata Rave, Veeva, and Inform.

    • Proficiency in Microsoft Office applications, including Outlook, Word, and Excel.

    Additional Competencies

    • Ability to work effectively in a fast-paced environment.

    • Strong problem-solving and analytical skills.

    • Ability to work independently and take initiative.

    • Good time management and the ability to complete tasks within deadlines.

    • Willingness to collaborate with cross-functional teams and support continuous improvement.

    Location & Salary

    Job locations: Bangalore and Chennai, India.

    Salary: The exact salary has not been disclosed in the supplied recruitment details. ICON states that it offers competitive compensation and country-specific employee benefits.

    Benefits at ICON

    The company lists several benefits, which may vary by country and employment arrangement:

    • Annual leave entitlements.

    • Health insurance options for employees and their families.

    • Retirement planning benefits.

    • Life assurance.

    • Employee assistance services through LifeWorks.

    • Country-specific benefits, which may include childcare support, gym membership discounts, travel benefits, and health assessments.

    Further information is available on the official ICON benefits page.

    How to Apply

    Eligible candidates can submit their applications through ICON’s official careers website.

    1. Open the official Elluminate Programmer vacancy.

    2. Review the role requirements and confirm that your programming experience matches the position.

    3. Update your résumé to highlight Elluminate report development, clinical data cleaning, data validation, and relevant programming languages.

    4. Include applicable experience with Veeva CDB, JReview, CDISC, SDTM, and clinical database systems.

    5. Complete the online application and submit the required information.

    Official Apply Link: Apply for Elluminate Programmer – ICON Careers

    Frequently Asked Questions

    1. What qualification is required for the ICON Elluminate Programmer position?

    A Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, Biology, or another health-related field is listed. Equivalent experience may also be considered if it provides the necessary skills and knowledge.

    2. How much experience is required?

    Candidates should have 3–5 years of experience programming listings and/or visualisations using Elluminate, Veeva CDB, or JReview. Hands-on Elluminate report development experience is also required.

    3. Can freshers apply for this vacancy?

    The role requires 3–5 years of relevant programming experience, so it is intended for experienced professionals rather than freshers.

    4. What programming languages are relevant to this role?

    Experience with at least one of CQL, SQL, SAS, R, or Python is required by the supplied job description.

    5. Where is the job located?

    The recruitment details mention Bangalore and Chennai, India, and list remote or office-based work options. Candidates should verify the specific arrangement on the official listing.

    6. What is the salary and last date to apply?

    The supplied details do not specify the salary or application deadline. Check the official ICON vacancy page for current information about compensation and application status.

    Job Summary Table

    Category Details
    Company ICON Strategic Solutions (FSP)
    Vacancies Elluminate Programmer / Lead Clinical Data Science Programmer
    Required Education Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, Biology, or another health-related field; equivalent experience may be considered
    Experience 3–5 years of relevant programming experience, including hands-on Elluminate report development
    Location Bangalore and Chennai, India; remote or office-based options listed

  • Roche Regulatory AI and Content Specialist Jobs

    Roche is inviting applications for the position of Regulatory AI and Content Specialist at Roche Services & Solutions in Hyderabad, Telangana. Candidates with a Bachelor’s or Master’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline are eligible to apply. Applicants should have 4–6 years of relevant pharmaceutical industry experience in Regulatory Affairs, Regulatory Operations, Regulatory Writing, Medical Writing, or related roles. The position focuses on regulatory content management, Generative AI-enabled authoring, and digital transformation of regulatory documentation.

    Roche Regulatory AI and Content Specialist Recruitment

    Company Overview

    Roche is a global healthcare company working across pharmaceuticals and diagnostics to advance medical science and improve patient care. Its work focuses on developing healthcare solutions that help address medical needs worldwide.

    Roche Services & Solutions (RSS) supports the organization through end-to-end business services, helping teams operate efficiently and focus on patient-centric activities. With a global network that includes Hyderabad and Chennai in India, RSS works across regions to deliver scalable business solutions.

    Within Roche Product Development, Product Development Regulatory (PDR) supports evolving regulatory requirements and global drug development priorities. The team uses automation, AI-enabled capabilities, and emerging technologies to improve regulatory processes and content development.

    Job Details

    • Company: Roche India – Roche Services & Solutions

    • Designation: Regulatory AI and Content Specialist

    • Department: Business Services & Support

    • Job Category: Business Services

    • Location: Hyderabad, Telangana, India

    • Experience: 4–6 years

    • Employment Type: Full-time, Regular/Permanent

    • Job ID: 202609-123378

    • Application Deadline: October 25, 2026, at 11:59 p.m. local time, based on the employer’s stated October 26 posting end date and its closing rule.

    Job Role & Responsibilities

    The Regulatory AI and Content Specialist will connect regulatory affairs expertise with content management and AI-enabled technology. The role involves preparing standardized regulatory content, maintaining reusable templates, supporting AI-assisted document authoring, and helping ensure regulatory documents are accurate, consistent, and ready for submission.

    Regulatory Content and AI Expertise

    • Apply knowledge of regulatory documents across the drug development lifecycle, including clinical, non-clinical, Chemistry, Manufacturing and Controls (CMC), and Common Technical Document (CTD)-based submissions.

    • Use Generative AI, structured content, and regulatory authoring principles to support content creation and document standardization.

    • Keep up with changing regulatory requirements, AI capabilities, and industry best practices.

    • Review regulatory, clinical, and safety documentation to support the development of structured content for AI-enabled authoring.

    Regulatory Content Management and Platform Administration

    • Analyze regulatory documents and convert them into standardized templates, reusable content components, and structured content models.

    • Configure and maintain templates, metadata, and content assets within Roche’s in-house Generative AI-powered platform.

    • Support compliant and efficient AI-assisted regulatory document authoring.

    • Maintain content governance through template lifecycle management, version control, and content quality processes.

    Platform Enablement and Collaboration

    • Act as a super user for the GenAI-powered platform, providing business support and helping users adopt its capabilities.

    • Contribute to continuous improvement initiatives that enhance platform adoption and operational efficiency.

    • Participate in User Acceptance Testing (UAT), business validation, and release-readiness activities for new platform features.

    • Collaborate with colleagues across Product Development Regulatory (PDR), Product Development (PD), Pharma Technical (PT), and Roche Digital Technology (RDT).

    • Identify opportunities to improve regulatory content development through AI, automation, and low-code/no-code technologies.

    AI-Enabled Regulatory Document Authoring

    • Work alongside regulatory document authors to support or lead the drafting of regulatory documents using AI-enabled authoring tools.

    • Assess whether AI-generated content is usable, accurate, consistent, and suitable for regulatory submissions.

    • Help align content structures and templates with regulatory requirements and business needs.

    Eligibility & Qualifications

    Candidates should meet the following educational, professional, and technical requirements.

    Educational Qualifications

    • Bachelor’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline.

    • Master’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline.

    Experience Requirements

    • 4–6 years of relevant experience in Regulatory Affairs, Regulatory Operations, Regulatory Writing, Medical Writing, or a related pharmaceutical role.

    • Experience leading or supporting clinical submissions or marketing authorization submissions.

    • Understanding of the drug development lifecycle, ICH guidelines, CTD/eCTD structure, and regulatory expectations of major health authorities.

    Technical Knowledge and Required Skills

    • Ability to critically review and interpret regulatory, clinical, and safety documents.

    • Knowledge of Generative AI, AI-enabled content authoring, and digital technologies.

    • Ability to convert regulatory information into standardized, structured content for AI-assisted authoring.

    • Strong analytical skills and attention to detail.

    • Excellent written communication and collaboration skills.

    • Effective stakeholder management and a continuous learning mindset.

    Preferred Experience

    The following experience would be beneficial:

    • Structured content authoring and document templating.

    • Content management and Regulatory Information Management (RIM) systems.

    • AI-enabled regulatory authoring platforms.

    • Low-code/no-code platforms.

    • Digital platform implementation, UAT, and business validation activities.

    Location & Salary

    Job location: Hyderabad, Telangana, India.

    The position is listed as full-time and regular/permanent under Roche Services & Solutions.

    How to Apply

    Interested and eligible candidates can apply through Roche’s official careers website.

    1. Open the official Roche job listing using the link below.

    2. Review the job description and eligibility requirements carefully.

    3. Complete the online application with accurate educational and professional details.

    4. Upload your updated résumé and any information requested in the application form.

    5. Submit the application and monitor your email for further communication from Roche.

    Official Apply Link: Regulatory AI and Content Specialist – Roche Careers

    Important Dates

    • Job posted: October 21, 2026

    • Posting end date: October 26, 2026

    • Application closing time: 11:59 p.m. on the previous day, according to the employer’s stated closing policy and the job location’s time zone.

    Candidates should apply promptly and verify the closing details on the official careers page.

    Documents Required

    Keep the following documents ready for the online application, as applicable:

    • Updated résumé or CV.

    • Educational qualification details and certificates.

    • Employment history and relevant work experience details.

    • Information about regulatory submissions, content management, or AI-enabled authoring experience.

    • Professional contact details.

    Follow the official application portal for the final list of required documents.

    Frequently Asked Questions

    1. What is the qualification required for the Roche Regulatory AI and Content Specialist role?

    Candidates need a Bachelor’s or Master’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline.

    2. How much experience is required?

    The advertised requirement is 4–6 years of experience in Regulatory Affairs, Regulatory Operations, Regulatory Writing, Medical Writing, or a related pharmaceutical role.

    3. Can freshers apply for this position?

    This vacancy is intended for experienced professionals. Freshers would not meet the stated 4–6 years of relevant experience requirement.

    4. What is the job location?

    The position is based in Hyderabad, Telangana, India, under Roche Services & Solutions.

    5. What is the salary for this vacancy?

    The salary has not been published in the supplied job details. Applicants can check the official recruitment page or discuss compensation during the hiring process.

    Job Summary Table

    Category Details
    Company Roche India – Roche Services & Solutions
    Vacancies Regulatory AI and Content Specialist
    Required Education Bachelor’s or Master’s degree in Life Sciences, Pharmacology, Regulatory Affairs, or a related discipline
    Experience 4–6 years in Regulatory Affairs, Regulatory Operations, Regulatory Writing, Medical Writing, or a related pharmaceutical role
    Location Hyderabad, Telangana, India

  • Dermatology sales Professionals Wanted Hyderabad Novartis

    Novartis Healthcare Private Limited is hiring for the position of Sales Representative (Territory Business Executive) in Hyderabad, Telangana. Candidates with a B.Sc. or B.Pharm qualification and at least 2 years of pharmaceutical sales experience, including 2 years in the Dermatology segment, are eligible to apply. A management degree is preferred. The role focuses on territory business development, specialty product promotion, healthcare professional engagement, and sales target achievement. Experienced pharmaceutical sales professionals with strong scientific knowledge and customer relationship skills can apply through the official Novartis careers portal.

    Novartis Sales Representative (Territory Business Executive) Recruitment

    Company Overview

    Novartis is a global pharmaceutical company focused on developing innovative medicines and improving patient outcomes. Its commercial teams work with healthcare professionals to communicate scientific and product information and support appropriate treatment decisions.

    Job Details

    • Company: Novartis Healthcare Private Limited

    • Designation: Sales Representative (Territory Business Executive)

    • Department: Sales

    • Business Unit: Marketing

    • Job Location: Hyderabad, Telangana, India

    • Experience: Minimum 2 years in pharmaceutical sales

    • Specialty Experience: Minimum 2 years in the Dermatology segment

    • Employment Type: Full-time, Regular

    • Job Requisition ID: REQ-10086732

    • Work Arrangement: Office-based, with territory-related customer engagement

    Job Role & Responsibilities

    The selected candidate will manage territory sales activities, promote specialty products, build relationships with healthcare professionals, and implement business plans aligned with brand strategy. The role also involves supporting new product launches, analyzing market information, and ensuring compliant customer engagement.

    Key Responsibilities

    Territory Business Management

    • Develop and execute territory business plans aligned with brand strategy.

    • Establish customer targeting, coverage plans, quarterly priorities, and sales cycle plans.

    • Monitor territory productivity and work toward defined sales objectives.

    • Support new product launches by ensuring market readiness.

    • Identify business opportunities and develop strategies to improve territory performance.

    Healthcare Professional Engagement

    • Build relationships with Key Opinion Leaders (KOLs) and other healthcare professionals.

    • Promote products through evidence-based, value-driven discussions.

    • Communicate relevant clinical and product information to healthcare professionals.

    • Address customer questions and objections effectively.

    • Improve understanding of disease management and patient treatment pathways.

    Sales Performance and Market Analysis

    • Use sales data, prescription insights, and market intelligence to improve customer targeting.

    • Optimize call effectiveness and territory-level sales activities.

    • Execute multichannel engagement strategies to improve customer coverage.

    • Monitor key performance indicators, including coverage, call quality, demand generation, and product availability.

    • Provide market insights to improve promotional effectiveness and sales forecasts.

    Distribution and Compliance

    • Coordinate with distribution and trade partners to maintain product availability.

    • Support alignment between primary and secondary sales.

    • Monitor stock availability, expiry risks, and supply-related concerns in priority channels.

    • Collaborate with cross-functional teams to improve resource allocation.

    • Maintain accurate and timely reporting.

    • Identify and resolve operational issues promptly.

    • Follow Novartis compliance requirements and ethical standards.

    Eligibility & Qualifications

    Educational Qualifications

    • B.Sc. in a relevant scientific discipline.

    • B.Pharm.

    • A management degree is preferred.

    Experience Required

    • Minimum 2 years of pharmaceutical sales experience.

    • Minimum 2 years of sales experience in the Dermatology segment.

    • Experience in specialty pharmaceutical sales is preferred.

    Required Skills

    • Strong scientific understanding of pharmaceutical products.

    • Ability to explain clinical and therapeutic benefits to healthcare professionals.

    • Knowledge of disease management and treatment protocols.

    • Ability to generate prescriptions and achieve sales targets.

    • Strong territory planning and business development skills.

    • Excellent communication and negotiation abilities.

    • Customer relationship management and stakeholder engagement.

    • Analytical skills for interpreting sales data and market intelligence.

    • Ability to work collaboratively with cross-functional teams.

    • Understanding of ethical pharmaceutical promotion and compliance requirements.

    Location & Salary

    • Job Location: Hyderabad, Telangana, India.

    • Company: Novartis Healthcare Private Limited.

    • Employment Type: Full-time, regular employment.

    How to Apply

    Eligible candidates can submit their applications through the official Novartis careers website.

    Application Process

    1. Visit the official job listing using the link below.

    2. Review the educational and experience requirements carefully.

    3. Update your resume with relevant pharmaceutical sales and Dermatology experience.

    4. Include details of territory management, sales performance, and healthcare professional engagement.

    5. Complete the online application and submit the required information.

    Official Apply Link: Apply for Sales Representative at Novartis

    Recruitment Contact for Accessibility Support

    Candidates requiring reasonable accommodation during the recruitment process can contact diversityandincl.india@novartis.com and include the job requisition number REQ-10086732 in their message.

    Documents Required

    Keep the following documents ready, as applicable:

    • Updated resume or CV.

    • B.Sc. or B.Pharm educational certificates.

    • Relevant work experience documents.

    • Details of Dermatology sales experience.

    • Sales performance records, where available.

    • Valid contact information.

    Additional Requirements

    • Candidates must meet the minimum pharmaceutical sales experience requirement.

    • At least two years of Dermatology sales experience is specified.

    • Applicants should be comfortable engaging healthcare professionals within the assigned territory.

    • Candidates should demonstrate the ability to develop territory business plans and achieve sales objectives.

    • Compliance with company policies and ethical promotional standards is essential.

    Frequently Asked Questions

    1. What qualification is required for the Novartis Territory Business Executive position?

    Candidates need a B.Sc. or B.Pharm qualification. A management degree is preferred.

    2. How much experience is required?

    Candidates need at least two years of pharmaceutical sales experience, including a minimum of two years in the Dermatology segment.

    3. Where is the job located?

    The position is based in Hyderabad, Telangana, India.

    4. What are the main responsibilities?

    The role involves territory sales management, specialty product promotion, healthcare professional engagement, new product launch support, market analysis, and sales target achievement.

    5. What is the salary offered by Novartis?

    The salary is not disclosed in the supplied recruitment details. Candidates should confirm compensation during the recruitment process.

    6. How can candidates apply?

    Candidates can apply through the official Novartis careers portal using the job link provided above.

    Job Summary Table

    Category Details
    Company Novartis Healthcare Private Limited
    Vacancies Sales Representative (Territory Business Executive)
    Required Education B.Sc. or B.Pharm; management degree preferred
    Experience Minimum 2 years in pharmaceutical sales, including 2 years in Dermatology
    Location Hyderabad, Telangana, India

  • Merck GOglobal Trainee R&D Recruitment 2027 | Pharmacometrics & Clinical Pharmacology | Bangalore

    Merck is inviting applications for the GOglobal Trainee R&D CMS position in Bangalore, Karnataka, under its Healthcare division. The opportunity is designed for candidates with a PhD in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, or a closely related discipline, including candidates nearing completion of their doctoral degree. Exceptional candidates with a master’s degree and strong quantitative research experience may also be considered. This structured 24-month rotational program focuses on pharmacometrics, Model-Informed Drug Development (MIDD), and quantitative drug development, with the next program start scheduled for June 2027.

    Merck GOglobal Trainee R&D CMS Recruitment

    Company Overview

    Merck operates across Healthcare, Life Science, and Electronics, using science and technology to develop solutions that support human health and scientific progress.

    Within its Healthcare division, the company develops medicines, medical devices, and technologies in therapeutic areas such as oncology, neurology, and fertility. Its Clinical Measurement Sciences (CMS) and quantitative pharmacology teams contribute to drug development through scientific modelling, clinical pharmacology, and data-driven decision-making.

    Job Details

    • Company: Merck

    • Designation: GOglobal Trainee R&D CMS

    • Program Focus: Pharmacometrics / Quantitative Pharmacology

    • Department: Research & Development (R&D), Clinical Measurement Sciences

    • Job Location: Bangalore, Karnataka, India

    • Employment Type: Full-time

    • Program Duration: 24 months

    • Next Start Date: June 2027

    • Job ID: 302954

    Job Role & Responsibilities

    The selected candidate will participate in a structured rotational program within the Quantitative Pharmacology team. The program is designed to develop expertise in Model-Informed Drug Development (MIDD) and its application throughout the drug development process, from early translational research to clinical decision-making.

    Key Responsibilities and Learning Areas

    • Develop expertise in pharmacometrics and quantitative drug development.

    • Apply Model-Informed Drug Development approaches to support scientific and clinical decisions.

    • Gain exposure to early translational science and clinical development activities.

    • Collaborate with teams working in Clinical Pharmacology and Translational Quantitative Pharmacology.

    • Work with Biostatistics, Biomarkers, and Patient-Focused Real-World Evidence teams.

    • Participate in three rotational assignments involving R&D functions in Bangalore, an international assignment at one of Merck’s global sites, and a return to Bangalore.

    • Build scientific, quantitative, and cross-functional skills relevant to long-term careers in drug development.

    • Apply mathematical and statistical methods to support pharmacological research and drug development decisions.

    Eligibility & Qualifications

    Educational Qualifications

    Candidates should meet one of the following educational requirements:

    • PhD in Pharmacometrics.

    • PhD in Clinical Pharmacology.

    • PhD in Applied Mathematics.

    • PhD in Statistics.

    • PhD in a closely related discipline.

    • Candidates in the final stages of completing a relevant PhD may also apply.

    • Exceptional candidates with a master’s degree and strong quantitative research experience may be considered.

    Required Technical Skills

    • Strong quantitative and mathematical foundation.

    • Knowledge of ordinary differential equations.

    • Understanding of parameter estimation techniques.

    • Mathematical or statistical programming skills.

    • Foundational understanding of clinical pharmacology.

    • Knowledge of the drug development process.

    Preferred Technical Experience

    Experience with pharmacokinetic and pharmacodynamic (PK/PD) modelling using industry-standard software is highly desirable.

    Relevant tools include:

    • NONMEM

    • R

    • Monolix

    Additional Competencies

    • Curiosity and a strong interest in scientific research.

    • Self-motivation and willingness to learn.

    • Ability to collaborate across multidisciplinary teams.

    • Interest in quantitative drug development and clinical research.

    • Commitment to continuous professional development.

    Location & Salary

    • Job Location: Bangalore, Karnataka, India.

    • Employment Type: Full-time.

    • Program Duration: 24 months.

    • International Exposure: Includes an international assignment at one of Merck’s global sites.

    • Salary: Not disclosed in the supplied recruitment announcement. Compensation should be confirmed during the recruitment process.

    How to Apply

    Eligible candidates can submit their applications through Merck’s official careers portal.

    Application Process

    1. Visit the official Merck job listing.

    2. Review the eligibility requirements and program details.

    3. Prepare an updated CV highlighting quantitative research, pharmacometrics, mathematical modelling, and programming experience.

    4. Include relevant academic qualifications and research experience.

    5. Complete the online application and submit the required information.

    Official Apply Link: Apply for GOglobal Trainee R&D CMS at Merck

    Selection Process

    Merck’s recruitment process may include application screening and interviews conducted by phone, video, or in person. The exact selection stages may vary depending on the position and location.

    Important Dates

    • Next Program Start Date: June 2027.

    • Application Deadline: Not specified in the supplied recruitment details.

    Candidates should visit the official careers page to check the current vacancy status and application availability.

    Documents Required

    Keep the following documents ready, as applicable:

    • Updated CV or resume.

    • PhD or master’s degree certificates, where applicable.

    • Academic transcripts.

    • Details of quantitative research projects.

    • Information about PK/PD modelling and programming experience.

    • Relevant research publications or supporting documents, if requested.

    Additional Requirements

    • Candidates should have a strong quantitative research background.

    • Applicants should be prepared for a rotational program involving an international assignment.

    • The role requires collaboration across scientific and R&D functions.

    • Experience with NONMEM, R, or Monolix is desirable.

    • Candidates should verify recruitment communications through Merck’s official channels and be cautious of fraudulent job offers.

    Frequently Asked Questions

    1. What qualification is required for the Merck GOglobal Trainee R&D CMS position?

    A PhD in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, or a closely related discipline is preferred. Candidates nearing completion of their PhD may also apply. Exceptional master’s degree holders with strong quantitative research experience may be considered.

    2. Can candidates with a master’s degree apply?

    Yes. The recruitment announcement states that exceptional candidates with a master’s degree and strong quantitative research experience may be considered.

    3. What is the duration of the GOglobal trainee program?

    The program lasts 24 months and includes three rotational assignments, including an international assignment at one of Merck’s global sites.

    4. Which technical skills are preferred?

    Candidates should have a strong quantitative foundation, knowledge of mathematical or statistical programming, and an understanding of clinical pharmacology. PK/PD modelling experience with NONMEM, R, or Monolix is highly desirable.

    5. Where is the job located?

    The position is based in Bangalore, Karnataka, India, with an international assignment included in the rotational program.

    6. When does the program begin?

    The next program start date is June 2027. Candidates should check the official job listing for current application details.

    Job Summary Table

    Category Details
    Company Merck
    Vacancies GOglobal Trainee R&D CMS
    Required Education PhD in Pharmacometrics, Clinical Pharmacology, Applied Mathematics, Statistics, or a related discipline; exceptional master’s candidates may be considered
    Experience Strong quantitative research experience; relevant PK/PD modelling experience is desirable
    Location Bangalore, Karnataka, India, with an international rotational assignment

  • Medanta Pharmacist Recruitment – D.Pharm / B.Pharm

    Medanta is inviting applications for the position of Pharmacist in its Retail Pharmacy department at the New HR Department in Gurgaon, Haryana.
    Candidates with D.Pharm or B.Pharm qualifications and 1–5 years of relevant experience are eligible to apply.
    Applicants must be registered with the Haryana Pharmacy Council, as specified in the recruitment announcement.
    Interested candidates can contact the recruitment team by phone or email to apply for this healthcare job opportunity.

    Medanta Recruitment: Pharmacist – Retail Pharmacy

    Company Overview

    Medanta is a healthcare organization offering career opportunities in pharmacy and healthcare services. The current opening is for a Pharmacist in the Retail Pharmacy department at its Gurgaon location.

    Job Role & Responsibilities

    Pharmacist – Retail Pharmacy

    The position is within the Retail Pharmacy department. The recruitment announcement does not provide a detailed list of job responsibilities.

    Typical responsibilities associated with retail pharmacy work may include:

    • Dispensing medicines according to valid prescriptions.

    • Checking prescriptions and supporting safe medication dispensing.

    • Maintaining pharmacy records and stock documentation.

    • Following applicable pharmacy regulations and medication-handling procedures.

    • Assisting patients with medicine-related queries within the pharmacist’s professional scope.

    Eligibility & Qualifications

    Candidates must meet the following requirements:

    • Educational Qualification: Diploma in Pharmacy (D.Pharm) or Bachelor of Pharmacy (B.Pharm).

    • Experience: 1–5 years.

    • Registration: Haryana-registered candidates only.

    • Department: Retail Pharmacy.

    • Job Designation: Pharmacist.

    Candidates should ensure that their pharmacy registration meets the employer’s stated requirement before applying.

    Location & Salary

    Job Location: New HR Department, Medanta, Gurgaon, Haryana.

    Salary details have not been provided in the recruitment announcement.

    How to Apply

    Interested candidates can contact Medanta’s recruitment team using the details below:

    Candidates should prepare an updated resume with their pharmacy qualification, relevant work experience and registration details.

    Important Instructions

    • Only candidates registered in Haryana are eligible, according to the recruitment announcement.

    • Applicants should have 1–5 years of relevant experience.

    • Candidates must hold a D.Pharm or B.Pharm qualification.

    • Contact the recruitment team for further application and selection details.

    Frequently Asked Questions

    1. What is the qualification required for the Medanta Pharmacist vacancy?

    Candidates must have a Diploma in Pharmacy (D.Pharm) or Bachelor of Pharmacy (B.Pharm).

    2. Can freshers apply for this Pharmacist position?

    The recruitment announcement specifies 1–5 years of experience. Freshers without relevant experience may not meet the stated requirement.

    3. Is Haryana pharmacy registration mandatory?

    Yes. The announcement specifies that only Haryana-registered candidates are eligible.

    4. Where is the Medanta Pharmacist job located?

    The position is at Medanta, New HR Department, Gurgaon, Haryana.

    5. How can candidates apply?

    Candidates can email their resume to Pharmacy.hiring@medanta.org or contact the recruitment team at 9045776181.

    6. What is the salary for this position?

    The salary has not been specified in the recruitment announcement. Candidates can contact the recruitment team for details.

    Job Summary

    Category Details
    Company Medanta
    Vacancies Pharmacist – Retail Pharmacy
    Required Education D.Pharm / B.Pharm
    Experience 1–5 years

  • Global Calcium QC Officer / Executive Recruitment

    Global Calcium is inviting applications for the position of QC Officer / Executive at its pharmaceutical manufacturing facility in Hosur, Tamil Nadu.
    Candidates with 2–6 years of experience in pharmaceutical quality control, instrumental analysis and standardization activities are encouraged to apply.
    This opportunity is suitable for professionals seeking to develop their careers in pharmaceutical Quality Control (QC).
    Interested candidates can send their updated resumes to the recruitment team by email.

    Global Calcium Recruitment: QC Officer / Executive

    Company Overview

    Global Calcium is a pharmaceutical company with manufacturing operations at Hosur, Tamil Nadu. The company is looking for quality control professionals to support its laboratory operations and maintain quality standards.

    Job Role & Responsibilities

    QC Officer / Executive

    The selected candidates will work in the Quality Control department and support laboratory testing and related QC activities.

    Key areas of experience include:

    • Instrumental analysis.

    • Standardization and related quality control activities.

    • Pharmaceutical industry quality control operations.

    Eligibility & Qualifications

    • Designation: QC Officer / Executive

    • Department: Quality Control (QC)

    • Experience Required: 2–6 years

    • Industry: Pharmaceutical

    • Relevant Skills: Instrumental analysis, standardization and related QC activities.

    Candidates should have relevant pharmaceutical industry experience and practical exposure to instrumental analysis and quality control procedures.

    Location & Salary

    Job Location: Global Calcium, Unit I & II, SIPCOT Industrial Complex, Phase I, Hosur, Tamil Nadu.

    Salary details have not been provided in the recruitment announcement.

    How to Apply

    Interested and eligible candidates can submit their updated resumes to the following email address:

    Email: gajapriya.k@globalcalciumpharma.com

    Candidates should include their relevant experience and current contact details in their resumes.

    Important Instructions

    • Candidates should have 2–6 years of relevant experience.

    • Experience in instrumental analysis and standardization is important for this position.

    • Applicants should have pharmaceutical industry experience.

    • Submit an updated resume through the email address provided above.

    Frequently Asked Questions

    1. What is the position available at Global Calcium?

    Global Calcium is hiring for the position of QC Officer / Executive.

    2. How much experience is required?

    Candidates with 2–6 years of relevant experience are eligible.

    3. What skills are required for this QC job?

    Experience in instrumental analysis, standardization and related quality control activities is required.

    4. Where is the job located?

    The position is based at Global Calcium, Unit I & II, SIPCOT Industrial Complex, Phase I, Hosur, Tamil Nadu.

    5. How can candidates apply?

    Candidates can email their updated resumes to gajapriya.k@globalcalciumpharma.com.

    6. Can freshers apply?

    The recruitment announcement specifies 2–6 years of experience, so the opening is intended for experienced candidates.

    Job Summary

    Category Details
    Company Global Calcium
    Vacancies QC Officer / Executive
    Required Education Not specified in the recruitment announcement
    Experience 2–6 years

  • Sagility Hiring Apprentice Trainee (Non-IT) – B.Pharm graduates preferred

    Sagility is inviting applications for the position of Apprentice Trainee (Non-IT) at its Coimbatore, Tamil Nadu, location. This opportunity is intended for freshers who completed their undergraduate degrees in 2024, 2025, or 2026, with candidates from healthcare-related backgrounds and B.Pharm preferred. The role involves healthcare operations, documentation, data entry, and compliance-related activities. Selected candidates will receive a monthly take-home salary of ₹14,000 and must be willing to work in the evening shift from 6:00 PM to 3:00 AM under the specified employment commitment.

    Sagility Apprentice Trainee Recruitment

    Company Overview

    Sagility provides technology-enabled business solutions and services to the healthcare industry. Its operations include healthcare administration and related support processes.

    Job Details

    • Company: Sagility

    • Designation: Apprentice Trainee

    • Department: Non-IT Healthcare Operations

    • Job Location: Coimbatore, Tamil Nadu, India

    • Experience: Freshers only

    • Eligible Graduation Years: 2024, 2025, and 2026, subject to the specific eligibility conditions in the recruitment post

    • Employment Type: Contract

    • Work Mode: On-site

    • Monthly Take-Home Salary: ₹14,000

    • Shift Timing: 6:00 PM to 3:00 AM

    • Commitment: 1-year contract followed by a stated 2-year confirmation period, amounting to a total three-year commitment

    Job Role & Responsibilities

    The selected candidates will learn and support non-IT healthcare operations, documentation, and data processing activities while following internal procedures and compliance guidelines.

    Key Responsibilities

    • Support routine healthcare operations.

    • Perform data entry and documentation activities.

    • Follow established compliance guidelines and work procedures.

    • Use internal tools to complete assigned tasks.

    • Maintain accuracy and attention to detail while handling information.

    • Coordinate with team members to complete assigned work.

    • Learn operational processes and follow instructions provided by supervisors.

    Eligibility & Qualifications

    Educational Qualifications

    The recruitment post specifies the following eligibility criteria:

    • Undergraduate degree holders from eligible healthcare-related backgrounds.

    • B.Pharm graduates are preferred.

    • Only freshers are eligible.

    • The hiring post identifies 2024, 2025, and 2026 graduates as the target groups, while also emphasizing 2025 and 2026 graduates in its eligibility summary.

    Candidates Who Should Not Apply

    According to the recruiter’s instructions, the following candidates are not eligible:

    • Postgraduates.

    • Diploma holders.

    • Engineering graduates.

    • Candidates from Business or Finance backgrounds.

    • IT-background candidates.

    • Experienced candidates.

    • Candidates from outside the specified location preference.

    Required Skills

    • Basic computer knowledge.

    • Willingness to learn healthcare operations.

    • Strong attention to detail.

    • Accuracy in data entry and documentation.

    • Good communication skills.

    • Ability to follow structured procedures and compliance requirements.

    Location & Salary

    • Job Location: Coimbatore, Tamil Nadu, India.

    • Work Arrangement: On-site, at the company office.

    • Monthly Take-Home Salary: ₹14,000.

    • Shift: Evening shift, 6:00 PM to 3:00 AM.

    • Employment Commitment: One-year contract followed by a stated two-year confirmation period.

    Candidates should clarify the employment terms, confirmation conditions, and any applicable contractual obligations with the recruiter before accepting the offer.

    How to Apply

    The recruiter has requested interested candidates to send their resumes directly through LinkedIn messaging.

    Application Process

    1. Open the LinkedIn job listing.

    2. Review the eligibility conditions carefully.

    3. Prepare an updated resume highlighting your undergraduate qualification and relevant skills.

    4. Send your resume directly to the job poster through LinkedIn messaging.

    5. Wait for further communication regarding the recruitment process.

    Official Job Listing: Apply for Apprentice Trainee at Sagility

    Recruiter: Mohammed Danish F.

    Interview and Selection Process

    The supplied recruitment post does not specify the interview rounds or selection procedure. Candidates should contact the recruiter through LinkedIn for further instructions.

    Important Dates

    The recruitment post does not provide a specific application deadline. Interested and eligible freshers should contact the recruiter to confirm whether applications are still being accepted.

    Documents Required

    Keep the following documents ready, as applicable:

    • Updated resume or CV.

    • Undergraduate degree certificate or provisional certificate.

    • Academic mark sheets.

    • Valid contact details.

    • Other documents requested by the recruiter.

    Additional Requirements

    • This is a non-IT opportunity.

    • Freshers only.

    • Candidates must be willing to work on-site in Coimbatore.

    • Applicants must be comfortable with the 6:00 PM to 3:00 AM shift.

    • The recruiter specifies a one-year contract followed by a two-year confirmation period.

    • Candidates should clarify the complete employment commitment and contractual conditions before joining.

    • Applications from excluded educational backgrounds or experienced candidates may not be considered.

    Frequently Asked Questions

    1. Can freshers apply for the Sagility Apprentice Trainee position?

    Yes. The recruitment post specifically targets freshers who completed eligible undergraduate degrees in the stated graduation years.

    2. Is B.Pharm eligible for this vacancy?

    B.Pharm is specifically mentioned as a preferred qualification. Candidates should confirm their eligibility with the recruiter before applying.

    3. What is the monthly salary?

    The stated monthly take-home salary is ₹14,000.

    4. Where is the job located?

    The position is on-site in Coimbatore, Tamil Nadu, India.

    5. What are the working hours?

    The stated shift is from 6:00 PM to 3:00 AM.

    6. How can candidates apply?

    Candidates should send their updated resume directly to the recruiter through LinkedIn messaging using the job listing provided above.

    Job Summary Table

    Category Details
    Company Sagility
    Vacancies Apprentice Trainee (Non-IT)
    Required Education Eligible undergraduate degree; healthcare-related backgrounds and B.Pharm preferred
    Experience Freshers only
    Location Coimbatore, Tamil Nadu, India