Category: Featured

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

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 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 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:

• Email: Pharmacy.hiring@medanta.org
• Mobile: 9045776181
• Careers Website: https://www.medanta.org/careers

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 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 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

Zytex Biotech is conducting a walk-in interview for multiple positions at its new fermentation unit in Manjusar GIDC, Vadodara, Gujarat. The company is hiring professionals for Upstream and Downstream Production, Seed and Inoculum Lab, Mechanical Engineering, Quality Control Microbiology and Bio-Agriculture Production.
Candidates with qualifications in Biotechnology, Microbiology, Chemistry, Agriculture and Mechanical Engineering can apply for the relevant positions.
The openings range from entry-level roles to senior management positions, with experience requirements varying by department.
The walk-in interview is scheduled for 25 October 2026, from 9:00 AM to 5:00 PM, at Pride Biznotel Hotel, Alkapuri, Vadodara.

Zytex Biotech Walk-In Interview: Department-Wise Vacancies

Company Overview

Zytex Biotech is expanding its team for its new fermentation unit in Manjusar GIDC, Vadodara, Gujarat. The recruitment drive includes opportunities in fermentation production, laboratory operations, mechanical maintenance, microbiology and bio-agriculture production.

Job Openings at Zytex Biotech

1. Officer / Executive / Senior Executive – Production (Upstream & Downstream)

• Experience: 2–18 years in fermentation or biotech production.
• Vacancies: 10 openings.
• Qualification: B.Sc. / M.Sc. in Microbiology, Biotechnology or Life Sciences; B.Tech / M.Tech in Biotechnology.

2. Officer / Senior Officer – Production Lab (Seed / Inoculum Lab)

• Experience: 2–7 years in an inoculum lab.
• Vacancies: 6 openings.
• Qualification: M.Sc. Biotechnology / Microbiology.

3. Executive – Maintenance & Utility (Mechanical Engineering)

• Experience: 6–10 years in process equipment and utilities maintenance.
• Vacancies: 5 openings.
• Qualification: B.Tech / B.E. in Mechanical Engineering.

4. QC – Microbiologist

• Gender Requirement: Male candidates only, as stated in the recruitment announcement.
• Experience: 2–5 years in a microbiology laboratory.
• Vacancies: 3 openings.
• Qualification: M.Sc. Biotechnology / Microbiology.

5. AM / Manager – Production (Upstream & Downstream)

• Experience: 15–18 years in fermentation or biotech production.
• Vacancies: 1 opening.
• Qualification: B.Sc. / M.Sc. in Microbiology, Biotechnology or Life Sciences; B.Tech / M.Tech in Biotechnology.

6. Manager – Production, Bio-Agriculture Plant

• Experience: 13–16 years in bio-agriculture or bio-fertilizer production.
• Vacancies: 1 opening.
• Qualification: M.Sc. / B.Sc. in Chemistry or Industrial Chemistry / Agriculture.

Job Role & Responsibilities

Production: Upstream and Downstream

• Support fermentation and biotechnological production activities.
• Work with relevant production processes and equipment.
• Follow established manufacturing procedures and operational requirements.

Production Lab: Seed and Inoculum

• Support laboratory operations related to seed and inoculum preparation.
• Follow applicable laboratory procedures and documentation practices.

Maintenance and Utilities

• Maintain process equipment and utility systems.
• Support equipment upkeep and maintenance activities.

Quality Control Microbiology

• Perform microbiology laboratory activities relevant to quality control.
• Follow applicable laboratory procedures and documentation requirements.

Bio-Agriculture Production

• Support production operations in the bio-agriculture or bio-fertilizer plant.
• Follow applicable manufacturing and operational procedures.

The responsibilities above are general descriptions of the listed roles. The recruitment poster provides specific experience and qualification requirements but does not include detailed job descriptions for every position.

Eligibility & Qualifications

The eligible qualifications vary by position:

• B.Sc. / M.Sc.: Microbiology, Biotechnology, Life Sciences, Chemistry, Industrial Chemistry or Agriculture, depending on the role.
• B.Tech / M.Tech: Biotechnology.
• B.Tech / B.E.: Mechanical Engineering.
• Experience: From 2 years for certain laboratory and microbiology roles to 18 years for senior production positions.

Candidates should match their education and experience to the specific vacancy before attending the interview.

Location & Salary

Work Location: New Fermentation Unit, Manjusar GIDC, Vadodara, Gujarat.

Salary details have not been specified in the recruitment announcement.

Walk-In Interview Details

• Company: Zytex Biotech
• Interview Date: Sunday, 25 October 2026
• Interview Time: 9:00 AM to 5:00 PM
• Venue: Pride Biznotel Hotel, Alkapuri, RC Dutt Road, Opposite Circuit House, Vadodara – 390007, Gujarat.
• Contact Number: 77779 20621
• Email: hr2.baroda@zytex.com

How to Apply

Interested candidates can attend the walk-in interview at the specified venue on 25 October 2026.

For recruitment-related queries, contact Zytex Biotech at 77779 20621 or email hr2.baroda@zytex.com.

Candidates should ensure that their qualifications and experience match the requirements of the position they wish to pursue.

Important Instructions

• Check the experience and qualification requirements for the selected role.
• The QC Microbiologist opening is specified for male candidates in the recruitment announcement.
• Attend the interview within the announced time window.
• Contact the recruitment team for any additional information about the selection process.

Frequently Asked Questions

1. Which positions are available at Zytex Biotech?

The openings include Production, Production Lab, Maintenance & Utility, QC Microbiologist, AM / Manager – Production and Manager – Production for the Bio-Agriculture Plant.

2. What qualifications are required?

Depending on the position, eligible qualifications include B.Sc., M.Sc., B.Tech, M.Tech and B.E. in relevant disciplines such as Biotechnology, Microbiology, Life Sciences, Chemistry, Agriculture and Mechanical Engineering.

3. How much experience is required?

The experience requirement varies by position, ranging from 2–5 years for QC Microbiologists to 15–18 years for AM / Manager – Production.

4. When is the walk-in interview?

The interview is scheduled for 25 October 2026, from 9:00 AM to 5:00 PM.

5. Where will the interview take place?

The venue is Pride Biznotel Hotel, Alkapuri, RC Dutt Road, opposite Circuit House, Vadodara – 390007, Gujarat.

6. How can candidates contact Zytex Biotech?

Candidates can call 77779 20621 or email hr2.baroda@zytex.com for recruitment-related queries.

Job Summary

Category	Details
Company	Zytex Biotech
Vacancies	Officer / Executive / Senior Executive – Production; Officer / Senior Officer – Production Lab; Executive – Maintenance & Utility; QC Microbiologist; AM / Manager – Production; Manager – Production, Bio-Agriculture Plant
Required Education	B.Sc. / M.Sc. / B.Tech / M.Tech / B.E. in relevant disciplines
Experience	2–18 years, depending on the position

Graviti Pharmaceuticals is conducting walk-in interviews for experienced candidates in its Oral Solid Dosage (OSD) formulation facility. The company is hiring Operators and Senior Operators for Production and Packing, along with Officers and Executives for Production / QMS.
Candidates with 2–8 years of relevant experience can apply for these pharmaceutical manufacturing jobs.
Immediate joiners are preferred for the available positions.
The walk-in interviews will be held from 22 October to 24 October 2026, between 10:00 AM and 1:00 PM, at Graviti Pharmaceuticals, Patancheru Mandal, Telangana.

Graviti Pharmaceuticals Walk-In Interview: Production, Packing and QMS

Company Overview

Graviti Pharmaceuticals is inviting applications for multiple positions at its OSD formulation facility. The recruitment drive is suitable for professionals with experience in pharmaceutical production, secondary packing and Quality Management System (QMS) activities.

Job Openings at Graviti Pharmaceuticals

1. Production Department

Area of Work: Compression

Designation: Operator / Senior Operator

Experience: 4–8 years

Candidates with relevant experience in pharmaceutical compression operations can apply for these positions.

2. Packing Department

Area of Work: Secondary Packing

Designation: Operator / Senior Operator

Experience: 4–8 years

Candidates with experience in secondary packing operations in pharmaceutical manufacturing facilities are eligible to attend.

3. Production / QMS Department

Area of Work: Not specified

Designation: Officer / Executive

Experience: 2–4 years

Professionals with relevant experience in pharmaceutical production or Quality Management System activities can consider this opportunity.

Job Role & Responsibilities

Production and Compression

• Support compression operations in the OSD manufacturing facility.
• Follow applicable manufacturing procedures and production requirements.
• Maintain proper documentation and comply with established quality standards.

Packing and Secondary Packing

• Support secondary packing operations.
• Follow packaging procedures and applicable documentation requirements.
• Maintain compliance with pharmaceutical manufacturing practices.

Production / QMS

• Support production-related activities and QMS procedures, as applicable to the assigned role.
• Maintain documentation and follow relevant quality requirements.

The responsibilities above describe typical activities associated with these roles. The recruitment announcement does not provide a detailed, position-wise responsibility list.

Eligibility & Qualifications

• Production: Operator / Senior Operator, Compression | 4–8 years of experience.
• Packing: Operator / Senior Operator, Secondary Packing | 4–8 years of experience.
• Production / QMS: Officer / Executive | 2–4 years of experience.

Candidates should have relevant pharmaceutical industry experience for the position they are applying for. The recruitment announcement does not specify the required educational qualifications.

Location & Salary

Work Location: Graviti Pharmaceuticals, Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307.

Salary details have not been provided in the recruitment announcement.

Walk-In Interview Details

• Company: Graviti Pharmaceuticals
• Interview Dates: 22–24 October 2026
• Days: Thursday to Saturday
• Time: 10:00 AM to 1:00 PM
• Venue: Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307
• Hiring Preference: Immediate joiners preferred

How to Apply

Interested candidates can attend the walk-in interview at the specified venue during the announced dates and timings.

Applicants should carry an updated resume and the relevant supporting documents for the interview.

Documents Required

Candidates should bring the following documents:

• Updated resume
• Salary slips for the last three months, if applicable
• Cost to Company (CTC) annexure, if applicable
• Educational documents
• Aadhaar card
• PAN card

Important Instructions

• Candidates should attend the interview between 10:00 AM and 1:00 PM on one of the scheduled dates.
• Immediate joiners are preferred.
• Carry the required documents for verification.

Frequently Asked Questions

1. Which positions are available at Graviti Pharmaceuticals?

The openings are for Operators and Senior Operators in Production and Packing, and Officers / Executives in Production / QMS.

2. How much experience is required?

Production and Packing positions require 4–8 years of experience. Production / QMS positions require 2–4 years.

3. Are immediate joiners preferred?

Yes. The recruitment poster states that immediate joiners are preferred.

4. When is the Graviti Pharmaceuticals walk-in interview?

The walk-in interview is scheduled from 22 October to 24 October 2026, between 10:00 AM and 1:00 PM.

5. Where is the interview venue?

The interview will take place at Graviti Pharmaceuticals, Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307.

6. What documents should candidates bring?

Candidates should bring an updated resume, the last three months’ salary slips if applicable, a CTC annexure if applicable, educational documents, an Aadhaar card and a PAN card.

Job Summary

Category	Details
Company	Graviti Pharmaceuticals
Vacancies	Operator / Senior Operator – Production (Compression); Operator / Senior Operator – Packing (Secondary Packing); Officer / Executive – Production / QMS
Required Education	Not specified in the recruitment announcement
Experience	Production / Packing: 4–8 years; Production / QMS: 2–4 years

Aculife Healthcare Private Limited is conducting a walk-in interview for the position of Production Chemist at its sterile manufacturing facility in Sachana Village, Viramgam, Ahmedabad, Gujarat. Candidates with B.Sc., M.Sc., B.Pharm or M.Pharm qualifications and 0–5 years of experience are eligible to attend.
The opening covers production activities in infusion, small-volume parenteral (SVP) and injectable manufacturing areas.
Applicants should have an understanding of GMP, safety standards, line clearance, batch documentation and in-process checks.
The walk-in interview is scheduled for 28 October 2026, from 8:00 AM to 11:00 AM, at Aculife Healthcare Private Limited, Gujarat.

Aculife Healthcare Recruitment: Production Chemist

Company Overview

Aculife Healthcare Private Limited is inviting applications for a Production Chemist position at its pharmaceutical manufacturing facility in Gujarat. The opportunity is suitable for freshers and experienced candidates interested in sterile pharmaceutical production.

Job Role & Responsibilities

Production Chemist: Key Responsibilities

Selected candidates will support production operations across infusion, small-volume parenteral (SVP) and injectable manufacturing areas.

Key responsibilities include:

• Operate and monitor production activities in sterile manufacturing areas.
• Maintain GMP compliance and follow safety standards.
• Perform line clearance and maintain batch records and production documentation.
• Conduct in-process checks and troubleshoot production-related issues.
• Maintain cleanliness and hygiene in the work area.
• Follow Quality Management System (QMS) procedures and regulatory requirements.

Eligibility & Qualifications

• Educational Qualifications: B.Sc. / M.Sc. / B.Pharm / M.Pharm.
• Experience: 0–5 years.
• Eligible Candidates: Freshers and experienced candidates.
• Department: Production.
• Work Areas: Infusion, SVP and injectable manufacturing.

Location & Salary

Job Location: Aculife Healthcare Private Limited, Sachana Village, Viramgam, Ahmedabad – 382150, Gujarat.

Salary details have not been specified in the recruitment announcement.

Walk-In Interview Details

• Company: Aculife Healthcare Private Limited
• Designation: Production Chemist
• Interview Date: 28 October 2026
• Interview Time: 8:00 AM to 11:00 AM
• Interview Type: Walk-in interview
• Venue: Sachana Village, Viramgam, Ahmedabad – 382150, Gujarat

How to Apply

Eligible candidates can attend the walk-in interview at the specified venue and time.

Candidates should carry an updated resume and the required supporting documents for verification during the interview.

Documents Required

Candidates should bring the following documents:

• Updated resume
• Educational certificates
• Experience certificates, if applicable
• Latest increment letter, if applicable
• Passport-size photograph
• Aadhaar card and PAN card

Important Instructions

• Candidates with 0–5 years of experience can attend the interview.
• Applicants should be prepared to discuss their knowledge of sterile manufacturing operations and GMP practices.
• Carry all applicable educational and employment documents to the interview.

Frequently Asked Questions

1. What is the qualification required for the Aculife Production Chemist position?

Candidates with B.Sc., M.Sc., B.Pharm or M.Pharm qualifications can apply.

2. Can freshers apply for this job?

Yes. The stated experience requirement is 0–5 years, so freshers are eligible.

3. When is the walk-in interview scheduled?

The interview is scheduled for 28 October 2026, from 8:00 AM to 11:00 AM.

4. Where is the job located?

The position is based at Aculife Healthcare Private Limited, Sachana Village, Viramgam, Ahmedabad, Gujarat.

5. What are the main responsibilities of a Production Chemist?

The role includes monitoring sterile production activities, maintaining GMP and safety compliance, performing line clearance, maintaining batch records and conducting in-process checks.

6. Which documents should candidates carry?

Candidates should bring an updated resume, educational certificates, applicable experience certificates, an increment letter if applicable, a passport-size photograph, Aadhaar card and PAN card.

Job Summary

Category	Details
Company	Aculife Healthcare Private Limited
Vacancies	Production Chemist
Required Education	B.Sc. / M.Sc. / B.Pharm / M.Pharm
Experienceyears	0–5

Caidya is inviting applications for the position of Clinical SAS Programmer in India, with the option to work remotely or from an office. Candidates with a bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science, or equivalent relevant work experience, can apply. The role requires 2–3 years of experience in statistical programming, with knowledge of SAS programming procedures, clinical trial data, and data reconciliation. This opportunity is suitable for professionals interested in clinical data management, statistical programming, and clinical research reporting.

Caidya Clinical SAS Programmer Recruitment

Company Overview

Caidya provides clinical research and development services to support clinical trials and pharmaceutical research. The company’s data operations teams work on programming, reporting, and data management activities that support clinical research projects.

Job Details

• Company: Caidya
• Designation: Clinical SAS Programmer
• Department: Clinical Data Management / Data Operations
• Job Location: India
• Work Arrangement: Remote or office-based
• Experience: 2–3 years in statistical programming
• Requisition ID: 8588

Job Role & Responsibilities

The Clinical SAS Programmer will support Caidya’s data operations by providing programming services to the Data Management department. The position works under the supervision of a Senior Clinical SAS Programmer and/or management and involves assigned programming, data checking, and reporting activities.

Key Responsibilities

• Develop complex data checks and data reconciliation reports.
• Create customized reports using SAS and other tools as requested by the Data Management department.
• Merge external data with Electronic Data Capture (EDC) data and check for consistency.
• Convert SAS datasets, delimited data files, and other file formats into Excel for data review.
• Automate reports to improve efficiency for team members.
• Collaborate and communicate with colleagues across local and international teams.
• Perform other duties as assigned.

Supervisory Responsibilities

This position does not include supervisory responsibilities.

Eligibility & Qualifications

Educational Qualifications

Candidates should have one of the following:

• Bachelor’s degree in Mathematics.
• Bachelor’s degree in Biostatistics.
• Bachelor’s degree in Statistics.
• Bachelor’s degree in Computer Science.
• Equivalent work experience demonstrating the required knowledge and skills.

Experience Required

• 2–3 years of experience providing statistical programming services.
• Knowledge of SAS DATA step programming.
• Familiarity with PROC IMPORT, PROC SQL, and ODS programming in SAS.
• Basic understanding of clinical trial databases and clinical trial data reports is preferred.

Required Skills

• Data merging, transposing, sorting, and other data manipulation techniques.
• Working knowledge of Microsoft Excel.
• Ability to understand reporting requests and select appropriate approaches for creating useful reports and listings.
• Problem-solving skills and the ability to work with limited supervision.
• Strong interpersonal and communication skills.
• Effective time management and organizational abilities.
• Ability to manage multiple projects simultaneously.
• Basic knowledge of UNIX, Windows, and PowerShell commands is preferred.
• Ability to work remotely when required.

Location & Salary

• Job Location: India.
• Work Arrangement: Remote or office-based.

Candidates should confirm compensation and other employment terms during the recruitment process.

How to Apply

Interested candidates can apply through Caidya’s official recruitment portal.

Application Process

1. Visit the official job listing using the link below.
2. Review the job requirements and responsibilities.
3. Prepare an updated resume highlighting SAS programming experience, data manipulation skills, and relevant clinical research exposure.
4. Complete the online application with accurate educational and professional details.
5. Submit the application through the recruitment portal.

Official Apply Link: Apply for Clinical SAS Programmer at Caidya

Recruitment Contact: careers@caidya.com

Important Recruitment Note

The company states that it does not accept unsolicited resumes from third-party vendors.

Important Dates

Candidates should check the official recruitment portal for the latest vacancy status and application availability.

Documents Required

Keep the following documents ready, as applicable:

• Updated resume or CV.
• Educational certificates and mark sheets.
• Details of relevant statistical programming experience.
• Information about SAS programming skills and clinical data management experience.
• Valid contact information.

Additional Requirements

• Candidates should be able to work collaboratively with local and international teams.
• Strong attention to detail is important when checking data consistency and preparing reports.
• Applicants should be comfortable handling multiple assignments and deadlines.
• The role requires the ability to work remotely when needed.
• Caidya is an equal opportunity employer and provides reasonable accommodation during the recruitment process for eligible individuals who require it.

Frequently Asked Questions

1. What qualification is required for the Caidya Clinical SAS Programmer position?

Candidates need a bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science. Equivalent work experience demonstrating the required skills may also be accepted.

2. How much experience is required?

The position requires 2–3 years of experience providing statistical programming services.

3. Is this a work-from-home opportunity?

The job listing allows candidates to work remotely or from an office in India.

4. Which SAS skills are required?

Candidates should know DATA step programming, PROC IMPORT, PROC SQL, and ODS programming. Familiarity with data manipulation and clinical trial databases is also relevant.

5. What is the salary offered by Caidya?

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

6. How can candidates apply?

Candidates can submit their applications through the official Caidya recruitment portal using the link provided above.

Job Summary Table

Category	Details
Company	Caidya
Vacancies	Clinical SAS Programmer
Required Education	Bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science, or equivalent relevant work experience
Experience	2–3 years in statistical programming
Location	India, remote or office-based