Author: Sudheer vanguri

OMNI Hospitals Hiring – Pharmacist | Kukatpally, Hyderabad

OMNI Hospitals, Kukatpally is hiring a Pharmacist for its healthcare team in Hyderabad. The opportunity is open to candidates with 0–3 years of experience who are interested in working in a hospital healthcare environment.

Pharmacist – OMNI Hospitals

Job Details

• Company: OMNI Hospitals
• Position: Pharmacist
• Location: Kukatpally, Hyderabad
• Experience: 0–3 Years
• Work Location: Near Kukatpally Metro Station, Balaji Nagar, Kukatpally, Hyderabad – 500072

Eligibility & Qualifications

The supplied recruitment post identifies the position as Pharmacist but does not specify the required educational qualification. Candidates should therefore verify the qualification requirements with OMNI Hospitals before applying.

Experience

• 0–3 Years

Job Opportunity

The position is for a Pharmacist to join the OMNI Hospitals, Kukatpally team and work within a healthcare environment.

The supplied post does not provide detailed responsibilities or specific technical requirements for the Pharmacist position.

Location & Experience

Location: Kukatpally, Hyderabad
Experience: 0–3 Years

Contact Details

For More Details: 7416871989
Email: careers@omnihospitals.in
Address: Near Kukatpally Metro Station, Balaji Nagar, Kukatpally, Hyderabad – 500072

How to Apply

Interested candidates can send their updated CV to:

Email: careers@omnihospitals.in

For additional details about the opportunity, contact 7416871989.

Job Summary

Tata Memorial Hospital Hiring – Clinical Research Coordinator | Mumbai

Tata Memorial Centre, Tata Memorial Hospital, Mumbai, is inviting applications for Clinical Research Coordinator under the RARExCAN – Establishing Rare Cancer and Exceptional Responders Network in India to Accelerate Translational Research project. The recruitment is for 1 position with an initial duration of 6 months and a monthly remuneration of ₹27,000. Candidates with B.Sc. Life Science or B.Pharm along with a mandatory PG Diploma in Clinical Research (PGDCR) can apply.

Clinical Research Coordinator – Tata Memorial Hospital

Job Details

• Organization: Tata Memorial Centre, Tata Memorial Hospital
• Position: Clinical Research Coordinator
• Project: RARExCAN – Establishing Rare Cancer and Exceptional Responders Network in India to Accelerate Translational Research
• Project Account No.: 6354
• No. of Posts: 01
• Initial Duration: 6 months
• Location: Mumbai
• Starting Remuneration: ₹27,000 per month
• Age Limit: 27 years
• Reference No.: TMC/AD/166/2026
• Advertisement Date: 28 September 2026

Clinical Research Coordinator – Job Responsibilities

The Clinical Research Coordinator will manage the daily operations of clinical trials and support the Principal Investigator and Co-Investigator in study-related activities.

Clinical Trial Responsibilities

• Assist the PI/Co-I with screening of trial participants.
• Support documentation of the Informed Consent (IC) process.
• Ensure protocol compliance.
• Coordinate with the Institutional Ethics Committee (IEC).
• Support clinical trial data management.
• Maintain the Investigator Study File.
• Process participant reimbursements.
• Maintain study-related trackers and logs.

Eligibility & Qualifications

Educational Qualification

• B.Sc. Life Science with Post Graduate Diploma in Clinical Research (PGDCR) – Mandatory

OR

• B.Pharm with Post Graduate Diploma in Clinical Research (PGDCR) – Mandatory

The official recruitment notice specifically states that the PGDCR is mandatory.

Age Limit

• Maximum Age: 27 years

Desirable Experience & Skills

• Experience handling global and multi-centric clinical trials is desirable.
• Good communication and people skills, both verbal and written.
• Fluency in English language is required as a desirable skill.

Eligible Qualification Courses

B.Sc. Life Science + PGDCR | B.Pharm + PGDCR

Application Process

Candidates must submit their candidature through the online application process only. The official notice states that candidates will initially be screened based on the information provided in the online application form.

Candidates called for an interview must carry original documents supporting their date of birth, qualifications and experience.

Important Application Details

Last Date to Apply: 02 October 2026
Last Time: 05:30 PM IST

Online Application:

Apply Online – Tata Memorial Centre

Incomplete applications will be rejected, and applicants are responsible for ensuring that they meet all eligibility criteria before applying.

Important Instructions

• Candidates must apply online only.
• Candidates called for an interview must carry original supporting documents.
• Internal candidates must submit an NOC from their current HOD/Principal Investigator.
• Tata Memorial Centre will not provide accommodation for outstation candidates.
• Candidates must provide a valid email ID, as recruitment-related correspondence and interview information will be communicated through email.
• For further enquiries, contact 24177000, Extension 4664 or email kevatncg.tmh@tmc.gov.in.

How to Apply

Eligible candidates should complete the Tata Memorial Centre online application before 02 October 2026 at 05:30 PM IST.

Tata Memorial Centre Official Online Application

Job Summary

ECLAT Health Solutions Mega Walk-In Drive – Certified Medical Coders | Navi Mumbai

ECLAT Health Solutions is conducting a Mega Walk-In Drive for experienced and certified Medical Coders in Navi Mumbai. The recruitment drive is open for professionals with expertise across Ancillary, Denials, EM, ED Profee, IVR, Pathology, Profee, Radiation Oncology and Surgery coding specialties.

Experienced Certified Medical Coders – ECLAT Health Solutions

Specialties Hiring

ECLAT Health Solutions is looking for experienced and certified Medical Coders with expertise in the following specialties:

• Ancillary
• Denials
• IVR
• EM with Surgery
• EM IP
• ED Profee
• Pathology
• Profee Observation
• Profee Surgery
• Radiation Oncology
• Surgery

Eligibility & Qualifications

Medical Coding Experience

• Experienced Medical Coders
• Certified Medical Coders
• Candidates should have relevant experience in one or more of the listed medical coding specialties.

The supplied recruitment details do not specify a particular certification such as CPC, CCS, COC or CIC, so no specific certification has been added as a mandatory requirement.

Medical Coding Specialties

Evaluation & Management Coding

• EM with Surgery
• EM IP
• ED Profee
• Profee Observation
• Profee Surgery

Specialty Coding

• Ancillary
• Denials
• IVR
• Pathology
• Radiation Oncology
• Surgery

Walk-In Interview Details

Company: ECLAT Health Solutions
Drive: Mega Walk-In Drive
Position: Experienced Certified Medical Coders
Location: Navi Mumbai
Date: 03 October 2026
Time: 10:00 AM – 5:00 PM

Walk-In Venue

14th Floor, D Wing, Empire Tower,
Reliable Cloud City, Gut No-31,
Navi Mumbai, Maharashtra – 400708

Candidates can scan the QR code provided in the recruitment poster and walk in directly.

How to Apply

Interested and eligible candidates can also apply through the ECLAT Health Solutions careers portal.

Apply for ECLAT Health Solutions Medical Coder Walk-In

Candidates attending the drive should carry their updated resume and relevant certification/experience documents.

Important Note

The supplied text describes 03 October 2026 as Friday, while 03 October 2026 falls on a Saturday. The date has been retained as 03 October 2026 rather than changing the source information.

Job Summary

Simson Pharma Walk-In Drive – Junior Purchase Officer & Chemistry Freshers | Hyderabad

Simson Pharma Ltd. is conducting a Walk-In Drive in Hyderabad for Junior Purchase Officer and Chemistry Fresher opportunities. Candidates with 0–1 year of experience can attend the recruitment drive at the company’s Kukatpally location between 1–3 October 2026.

Junior Purchase Officer – Purchase Department

Job Responsibilities & Requirements

• Basic knowledge of purchase activities
• Basic knowledge of vendor coordination
• Knowledge of Tally is required
• Male candidates preferred

Eligibility & Qualifications

• Any Degree

Experience

• 0–1 Year

Walk-In Details

• Walk-In Dates: 01–03 October 2026
• Time: 11:00 AM – 4:00 PM
• Location: Kukatpally, Hyderabad

Chemistry Freshers – Analytical & Organic Chemistry

Simson Pharma Ltd. is also hiring fresh talent for Analytical Chemistry and Organic Chemistry positions.

Available Areas

• Analytical Chemistry
• Organic Chemistry

Eligibility & Qualifications

• M.Sc. Analytical Chemistry
• M.Sc. Organic Chemistry
• M.Pharm

Experience

• 0–1 Year

Walk-In Interview Details

Dates: 01–03 October 2026
Time: 11:00 AM – 4:00 PM
Venue: Shed No. 6A, Type-III, Prashanthi Nagar, IDA, Kukatpally, Hyderabad – 500037

Contact Details

HR: 7799883045 / 9652187209
Email: hr.hyd@simsonpharma.com

Candidates should carry their updated CV when attending the walk-in drive.

Eligible Qualification Courses

Any Degree | M.Sc. Analytical Chemistry | M.Sc. Organic Chemistry | M.Pharm

How to Apply

Eligible candidates can attend the Simson Pharma Ltd. Walk-In Drive at the above-mentioned venue between 11:00 AM and 4:00 PM from 01–03 October 2026.

Candidates attending the Chemistry Fresher drive can contact HR at 7799883045 / 9652187209 or email hr.hyd@simsonpharma.com.

Job Summary

IQVIA Hiring – Sr. CRA1 | Clinical Research | Thane, Bengaluru, Hyderabad & Noida

IQVIA is hiring Sr. CRA1 professionals for its Clinical Research team across multiple locations in India. The role focuses on clinical trial site monitoring, site management, subject recruitment, protocol compliance, regulatory submissions, TMF and ISF documentation, and Good Clinical Practice (GCP) requirements.

Sr. CRA1 – Clinical Research

Job Details

• Company: IQVIA
• Position: Sr. CRA1
• Job ID: R1571208
• Employment Type: Full-time
• Work Mode: Hybrid
• Primary Location: Thane, India
• Additional Locations: Bengaluru, Hyderabad, Noida

Job Overview

The Sr. CRA1 will perform monitoring and site management activities to ensure that clinical trial sites conduct studies and report study data according to the study protocol, applicable regulations and guidelines, and sponsor requirements.

Key Responsibilities

Clinical Trial Site Monitoring

• Perform site monitoring visits, including:

  • Site selection
  • Site initiation
  • Monitoring visits
  • Close-out visits

• Conduct monitoring activities in accordance with the contracted scope of work and Good Clinical Practice (GCP).
• Evaluate the quality and integrity of study site practices related to proper protocol conduct.
• Ensure adherence to applicable regulations and escalate quality issues when appropriate.

Subject Recruitment & Site Management

• Work with clinical trial sites to adapt, drive and track subject recruitment plans according to project requirements.
• Support recruitment predictability and project delivery.
• Administer protocol and related study training to assigned sites.
• Establish regular communication with sites to manage project expectations and resolve ongoing issues.

Study Progress & Regulatory Activities

• Track the progress of assigned studies, including:

  • Regulatory submissions and approvals
  • Recruitment and enrollment
  • Case Report Form (CRF) completion and submission
  • Data query generation and resolution

• Support the study start-up phase when required.

TMF & ISF Documentation

• Ensure required site documents are available for filing in the Trial Master File (TMF).
• Verify that the Investigator’s Site File (ISF) is maintained according to GCP and local regulatory requirements.
• Create and maintain documentation relating to:

  • Site management
  • Monitoring visit findings
  • Action plans

• Submit regular visit reports and generate follow-up letters and other required study documentation.

Collaboration & Project Support

• Collaborate and liaise with study team members to support project execution.
• Where applicable, support development of project-specific subject recruitment plans on a site-by-site basis.
• Where applicable, support site financial management according to executed clinical trial agreements.
• Retrieve invoices according to local requirements.

Eligibility & Qualifications

Educational Qualification

• Bachelor’s Degree in a scientific discipline or healthcare – preferred and required according to the source listing.
• An equivalent combination of education, training and experience may be accepted in lieu of a degree.

Experience

• At least 2 years of on-site monitoring experience – Required

Required Knowledge & Skills

• Good knowledge and ability to apply applicable clinical research regulatory requirements.
• Knowledge of Good Clinical Practice (GCP).
• Knowledge of International Council for Harmonisation (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided through company training.
• Proficiency in:

  • Microsoft Word
  • Microsoft Excel
  • Microsoft PowerPoint

• Ability to use laptop computers and applicable mobile devices.
• Strong written and verbal communication skills.
• Good command of the English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Eligible Qualification Courses

The source specifies a Bachelor’s Degree in a scientific discipline or healthcare rather than specific courses. Relevant examples include:

B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences | Biotechnology | Microbiology | Biochemistry | Biomedical Sciences | Other relevant Scientific or Healthcare disciplines

Location & Work Mode

Primary Location: Thane, India
Additional Locations:

• Bengaluru, India
• Hyderabad, India
• Noida, India

Work Mode: Hybrid
Employment: Full-time

How to Apply

Interested and eligible candidates can apply through the official IQVIA careers portal.

Apply for Sr. CRA1 – IQVIA

Job Summary

IQVIA Hiring – Site Activation Specialist 1 | Clinical Research | Bengaluru

IQVIA is hiring a Site Activation Specialist 1 for its Clinical Research team in Bengaluru. The role focuses on site feasibility, site identification, start-up and activation activities, along with regulatory, ethics, contractual and document management for clinical research studies.

Site Activation Specialist 1 – Clinical Research

Job Details

• Company: IQVIA
• Position: Site Activation Specialist 1
• Job ID: R1571200
• Location: Bengaluru, India
• Employment Type: Full-time
• Work Mode: Hybrid

Job Overview

The Site Activation Specialist performs country-level activities associated with Site Activation (SA) in accordance with applicable local and international regulations, standard operating procedures, project requirements and contractual or budgetary guidelines.

The position is a professional individual contributor role working under moderate supervision and is also responsible for recommending enhancements to systems and processes to improve effectiveness.

Key Responsibilities

Site Feasibility & Activation

• Serve as the Single Point of Contact (SPOC) for assigned studies involving:

  • Investigative sites
  • Site Activation Managers (SAMs)
  • Project Management teams
  • Other relevant departments

• Ensure adherence to SOPs, Work Instructions (WIs), quality requirements and project timelines.
• Perform:

  • Feasibility activities
  • Site identification
  • Study start-up activities
  • Site activation activities

• Distribute completed documents to sites and internal project team members.

Site & Document Management

• Prepare site documents and review them for completeness and accuracy.
• Ensure accurate completion and maintenance of internal systems, databases and tracking tools.
• Review, track and follow up on the progress, approval and execution of:

  • Questionnaires
  • CDA/SIF
  • Regulatory documents
  • Ethics documents
  • Informed Consent Forms (ICFs)
  • Investigator Pack (IP) release documents

• Perform quality control of documents provided by clinical research sites.

Project Planning & Timelines

• Review, establish and agree on project planning and timelines.
• Ensure appropriate monitoring measures are in place.
• Implement contingency plans when required.
• Inform team members when feasibility, site identification, regulatory and contractual documents for individual sites are completed.
• Provide local expertise to Site Activation Managers and project teams during initial and ongoing project timeline planning.

Performance & Stakeholder Coordination

• Review site performance metrics and provide feedback to management.
• Maintain project-specific information in internal systems and tracking tools.
• May have direct contact with sponsors on specific initiatives.
• Coordinate with investigative sites, project teams and other departments to support study activation activities.

Eligibility & Qualifications

Educational Qualification

• Bachelor’s Degree in Life Sciences or a related field – Required

Experience

The supplied job description lists the following experience requirements:

• 3 years of clinical research or other relevant experience, or equivalent combination of education, training and experience.
• It also specifically states:

  • 3 years of clinical research experience
  • Including 1 year of experience in a leadership capacity

• Equivalent combination of education, training and experience may be considered.

Eligible Qualification Courses

B.Pharm | M.Pharm | Pharm.D | B.Sc. Life Sciences | M.Sc. Life Sciences | Biotechnology | Microbiology | Biochemistry | Clinical Research | Biomedical Sciences | Other relevant Life Sciences qualifications

The source specifically states a Bachelor’s degree in Life Sciences or a related field; the course examples above are aligned examples rather than individually listed mandatory degrees in the source.

Key Skills & Knowledge Areas

• Clinical Research
• Site Activation
• Site Feasibility
• Site Identification
• Clinical Trial Start-Up
• Regulatory Documentation
• Ethics Documentation
• Investigator Site Management
• Informed Consent Forms
• Investigator Pack Documentation
• SOP Compliance
• Work Instructions
• Quality Control
• Project Timeline Management
• Clinical Research Documentation
• Stakeholder Coordination
• Site Performance Tracking

Location & Work Mode

Location: Bengaluru, India
Work Mode: Hybrid
Employment: Full-time
Job ID: R1571200

How to Apply

Interested and eligible candidates can apply through the official IQVIA careers portal.

Apply for Site Activation Specialist 1 – IQVIA

Job Summary

Parexel Hiring – Medical Writer I / Medical Writer II | Patient Safety

Parexel is hiring Medical Writer I / Medical Writer II – Patient Safety for its Medical Affairs team in India. The role focuses on pharmacovigilance, aggregate safety reports, signal detection and evaluation, literature review, Risk Management Plans and regulatory safety documentation. Candidates with Life Sciences, Health or Biomedical Sciences qualifications and relevant pharmacovigilance or medical writing experience can apply.

Medical Writer I / Medical Writer II – Patient Safety

Job Details

• Company: Parexel
• Position: Medical Writer I / Medical Writer II
• Category: Medical Affairs
• Job ID: R0000046349
• Primary Location: Hyderabad, India
• Additional Locations: Bengaluru, India; Remote, India; Mohali, India
• Work Mode: Hybrid / On-site / Remote, as applicable

About Parexel

Parexel is a global clinical development partner providing clinical and consulting solutions to the life sciences industry. The company works with biopharmaceutical companies and research sites to support clinical trials and the development of new therapies.

Medical Writer I – Patient Safety

Key Responsibilities

• Prepare, compile and lead the development of scheduled and ad-hoc aggregate safety reports, including:

  • Periodic Safety Update Reports (PSURs)
  • Periodic Benefit-Risk Evaluation Reports (PBRERs)
  • Development Safety Update Reports (DSURs)
  • Other regulatory safety documents

• Conduct independent signal detection using safety data from databases, clinical data, literature and regulatory websites.
• Apply quantitative and qualitative methodologies to identify potential safety signals.
• Prepare Drug Safety Reports (DSRs) and Signal Evaluation Reports (SERs).
• Conduct systematic literature searches and reviews to summarize safety data and identify emerging safety trends.
• Support signal evaluation and epidemiology assessments.
• Manage signal tracking activities and maintain comprehensive signal logs.
• Identify and resolve discrepancies in safety data sources.
• Ensure data integrity across safety deliverables.
• Assist with preparing and updating Risk Management Plans (RMPs) and related documents.
• Manage routine client interactions and queries.
• Maintain audit-ready documentation and properly archive source materials.
• Support inspection-readiness activities and regulatory compliance.

Medical Writer II – Patient Safety

In addition to the responsibilities above, the Medical Writer II role includes:

• Mentor junior team members on technical and soft skills.
• Provide constructive feedback.
• Lead complex client discussions.
• Manage multi-stakeholder document review cycles.
• Contribute to process improvement initiatives.

Eligibility & Qualifications

Educational Qualification

Candidates should have a University degree in Life Sciences, Health or Biomedical Sciences, such as:

• Pharmacy
• Microbiology
• Biochemistry
• Biotechnology
• Biophysics
• Dentistry
• Physiotherapy

An equivalent combination of training and work experience may also be considered.

Experience

Medical Writer I:

• 2+ years of experience in Pharmacovigilance, Medical Writing or a related field.

Medical Writer II:

• 4+ years of experience in Pharmacovigilance, Medical Writing or a related field.

Required Skills

• Strong analytical thinking
• Scientific writing
• Problem-solving
• Pharmacovigilance knowledge
• Understanding of global pharmacovigilance regulations
• Medical terminology and safety-related concepts
• Medical writing tools
• Microsoft Office applications
• Pharmacovigilance databases
• Coding dictionaries such as MedDRA and WHO-DD
• Strong communication and organizational skills
• Excellent time management
• Ability to prioritize multiple concurrent projects
• Attention to detail
• Ability to work with internal teams and external clients

Preferred Qualifications

• Prior experience in Pharmacovigilance or safety assessment
• Clinical exposure in hospital-based environments
• Direct clinical research experience
• Expertise in specific therapeutic areas or product types
• Familiarity with pharmacovigilance systems
• Understanding of regulatory submission processes across multiple regions

Eligible Qualification Courses

B.Pharm | M.Pharm | Pharm.D | B.Sc. Microbiology | M.Sc. Microbiology | B.Sc. Biochemistry | M.Sc. Biochemistry | B.Sc. Biotechnology | M.Sc. Biotechnology | Biophysics | BDS | BPT | Other relevant Life Sciences, Health or Biomedical Sciences qualifications

Location & Work Mode

Primary Location: Hyderabad, India

Additional Locations:

• Bengaluru
• Remote, India
• Mohali

Work Mode: Hybrid / On-site / Remote, depending on the applicable position and location.

How to Apply

Interested and eligible candidates can apply through the official Parexel careers portal.

Apply for Medical Writer I / Medical Writer II – Parexel

Job Summary

Sanzyme is hiring professionals for its Quality Control (QC) team at the Formulation Unit in Telangana.
The openings include Senior Executive – QC and In-Process QC positions for male candidates.
Candidates with B.Pharm or B.Sc. qualifications and relevant pharmaceutical QC experience can apply.
Immediate joiners will be preferred for these Quality Control opportunities.

Sanzyme Quality Control: Job Details

Sanzyme Pvt. Ltd. is inviting applications for QC positions at its Formulation Unit, Kolthur Village, Shamirpet, Telangana.

Sanzyme QC: Current Openings

1. QC | Senior Executive | Male

Qualification: B.Pharm / B.Sc.
Experience: 8–10 Years
Work Area: QC and QMS activities
Preference: Immediate joiners will be preferred.

2. In-Process QC | Male

Qualification: B.Pharm / B.Sc.
Experience: 0–2 Years
Work Area: In-Process QC
Preference: Immediate joiners will be preferred.

Sanzyme QC: Eligibility & Qualifications

Candidates with the following qualifications are eligible to apply:

B.Pharm | B.Sc.

Sanzyme QC: Experience Requirements

• Senior Executive – QC: 8–10 years of relevant experience.
• In-Process QC: 0–2 years of relevant experience.
• Candidates with experience in pharmaceutical Quality Control and related activities can apply for the relevant position.

Sanzyme QC: Job Responsibilities

Sanzyme Senior Executive – QC

The Senior Executive position involves working in Quality Control and QMS activities within the formulation manufacturing environment.

Relevant responsibilities may include:

• Supporting routine Quality Control activities.
• Handling QC documentation and related records.
• Supporting QMS-related activities and compliance requirements.
• Coordinating with relevant departments for quality-related activities.
• Ensuring assigned QC activities are completed according to applicable procedures.

Sanzyme In-Process QC

The In-Process QC role focuses on quality checks during pharmaceutical manufacturing operations.

Key activities include:

• Performing in-process quality checks.
• Supporting routine QC activities during manufacturing.
• Maintaining relevant QC documentation and records.
• Following applicable SOPs and quality procedures.
• Coordinating with production and QC teams as required.

How to Apply

Interested candidates can share their updated resume through WhatsApp or email.

WhatsApp: 7032837394

Email: ramakrishna.reddy@sanzyme.com

Sanzyme QC Job Location

Sanzyme Pvt. Ltd. – Formulation Unit
Kolthur Village, Shamirpet,
Telangana.

Job Summary

Ipca Laboratories Limited is conducting a Walk-In Interview for freshers for its Center of Excellence (CoE) training initiative in the Production API department.
The program is designed to provide hands-on industrial exposure to students looking to build a career in the pharmaceutical industry.
Eligible B.Sc. Chemistry and B.Tech Chemical pass-outs can attend the walk-in interview for the Production API training program.
The three-month training includes a ₹12,300 monthly stipend, with career progression opportunities after successful completion of the program.

Ipca Laboratories Production API: Walk-In Interview Details

Ipca Laboratories Ltd. has launched its Center of Excellence (CoE) as a specialized training initiative aimed at providing practical industrial exposure to students aspiring to build a career in the pharmaceutical industry.

The program is designed to enhance participants’ practical understanding of the Production Department and prepare them for real-world applications in pharmaceutical manufacturing.

Ipca Laboratories Production API: Walk-In Interview Schedule

• Date: Saturday, 3rd October 2026
• Time: 10:00 AM to 16:00 hrs
• Venue: Ipca Laboratories Limited, Plot No. 16-22, Industrial Area No. 1, AB Road, Dewas, Madhya Pradesh

Ipca Laboratories Production API: Eligibility & Qualifications

Educational Qualification

Candidates meeting the following qualification criteria are eligible:

B.Sc. Chemistry | B.Tech. Chemical

• Pass-out year: 2023–2026
• The opportunity is intended for freshers interested in pharmaceutical production and API manufacturing.

Ipca Laboratories Production API: Training Details

Department

Production – API

Center of Excellence Training

The CoE training program provides participants with hands-on industrial exposure and practical understanding of pharmaceutical API production operations.

The training duration is 3 months.

Stipend

₹12,300 per month

Other Facilities

• Free canteen
• Transportation facility

Ipca Laboratories Production API: Career Progression

Upon successful completion of the 3-month CoE training program, candidates will be absorbed at Ipca Laboratories Ltd., Renukoot, Dewas API and Wardha API on CTC packages of:

• ₹2.55 LPA
• ₹2.65 LPA
• ₹3.45 LPA

The applicable CTC will depend on compatibility and skills.

How to Apply

Interested candidates should attend the walk-in interview with their updated resume.

Candidates are advised to carry the required documents and attend the interview at the specified venue and time.

Ipca Laboratories Recruitment Disclaimer

Ipca Laboratories Ltd. does not charge any fees from candidates at any stage of the recruitment process. Candidates should not respond to or make payments against recruitment-related requests.

Any demand for payment by a recruiter or agency claiming to represent Ipca Laboratories Ltd. should be reported immediately to:

ipca@ipca.com
corporate.communication@ipca.com

Job Summary

Sudeep Pharma Limited is hiring candidates for the Quality Control (QC) Department at its Nandesari GIDC facility in Vadodara.
The opening is for QC Trainee / QC Chemist with 0–2 years of experience, including freshers.
Candidates with a B.Sc. or M.Sc. in Chemistry can apply for this pharmaceutical quality control opportunity.
The role offers exposure to analytical testing, laboratory practices, GMP, GLP and data integrity requirements.

Sudeep Pharma Limited QC Trainee / QC Chemist

Sudeep Pharma Limited QC Department: Job Details

Company: Sudeep Pharma Limited
Department: Quality Control
Position: QC Trainee / QC Chemist
Location: Nandesari GIDC, Vadodara, Gujarat
Experience: 0–2 Years
Freshers: Can apply

Sudeep Pharma Limited QC Trainee / QC Chemist: Eligibility & Qualifications

Candidates with the following qualifications are eligible:

B.Sc. Chemistry | M.Sc. Chemistry

Sudeep Pharma Limited QC Trainee / QC Chemist: Desired Candidate Profile

• B.Sc. / M.Sc. in Chemistry.
• 0–2 years of experience in Pharmaceutical Quality Control.
• Freshers are encouraged to apply.
• Basic knowledge of analytical instruments and laboratory practices.
• Good communication skills and a willingness to learn.
• Team player with attention to detail.

Sudeep Pharma Limited QC Trainee / QC Chemist: Key Responsibilities

Quality Control Analysis

• Analysis of raw materials, in-process samples, finished products and stability samples.
• Operate analytical instruments such as UV, FTIR, KF and pH meter.
• Maintain analytical records and reports.
• Perform routine laboratory activities and support instrument calibration.

Sudeep Pharma Limited QC: GMP & Laboratory Compliance

• Ensure compliance with GMP and GLP requirements.
• Maintain data integrity in laboratory activities.
• Follow applicable laboratory procedures and documentation practices.
• Maintain attention to detail during testing and documentation.

Why Join Sudeep Pharma Limited QC Department?

The position provides an opportunity to work in a modern QC laboratory and develop practical pharmaceutical quality control skills. The organization highlights career growth opportunities, learning and development, and a supportive work culture.

How to Apply

Interested candidates can send their updated CV to:

Email: tanmay.talati@sudeepgroup.com

Candidates can apply by sending their updated resume to the above email address.

Job Summary