Pharma STUFF

15/03/2026

Vantive Hiring – Research Associate II (Pharma R&D)

Looking to grow your Pharmaceutical R&D career?
Vantive is hiring Research Associate II – Renal Solutions in Bangalore.

🎓 Eligibility: MSc Chemistry / MPharm / PhD (Pharma or Chemistry)
⏳ Experience: 4+ Years Pharmaceutical R&D
📍 Location: Whitefield, Bangalore

Work on product development, lifecycle management & renal therapy innovations.

Apply Now 👇
https://pharmastuff.org/job/vantive-research-associate-renal-solutions

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15/03/2026

I𝐐𝐕𝐈𝐀 𝐇𝐢𝐫𝐢𝐧𝐠 – 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐑𝐞𝐬𝐞𝐚𝐫𝐜𝐡 𝐀𝐬𝐬𝐨𝐜𝐢𝐚𝐭𝐞 𝐈𝐈 (𝐂𝐑𝐀 𝟐)

🎓 Eligibility: Pharmacy / Life Sciences / Nursing
⏳ Experience: 1+ Year Clinical Trial Monitoring

Apply Now 👇
https://pharmastuff.org/job/iqvia-hiring-cra-2

14/03/2026

Syneos Health Hiring – Pharmacovigilance Coordinator

🏢 Company: Syneos Health

📍 Location: Gurgaon

💼 Role: Drug Safety / Pharmacovigilance

🎓 Eligibility: B.Pharm / M.Pharm / PharmD / BDS

⏳ Experience: Minimum 1 Year PV / ICSR Processing

Work on clinical trial safety cases & pharmacovigilance databases.

🔗 Apply Now https://pharmastuff.org/job/syneos-health-safety-pharmacovigilance-coordinator

14/03/2026

Labcorp Hiring – Data Management Associate I (Entry Level)

Looking to start your career in Clinical Data Management?
Labcorp is hiring Data Management Associate I in Bangalore.

🎓 Qualification: Pharmacy / Life Sciences / Statistics / Computer Science
📍 Location: Bangalore
🕑 Shift: 2 PM – 11 PM

Work on clinical study databases, data review, and research data management.

Apply Now 👇
https://pharmastuff.org/job/labcorp-data-management-associate-i

13/03/2026

Fortrea Pharmacovigilance Safety Specialist I

Fortrea is hiring Specialist I – Clinical Safety in Bangalore for professionals with 1–2 years PV experience.

🎓 Qualification: Pharmacy / Life Sciences

💼 Department: Pharmacovigilance / Drug Safety

📍 Location: Bangalore

Work on AE/SAE case processing, MedDRA coding & global safety reporting.

Apply Now 👇

https://pharmastuff.org/job/fortrea-pharmacovigilance-safety-specialist-i

13/03/2026

Fortrea Hiring Pharmacovigilance – Safety Science Analyst (Freshers Eligible)

🎓 Eligibility: B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Life Sciences
⏳ Experience: 0–1 Year
📄 Type: 6-Month Contract

👉 Apply Now
https://pharmastuff.org/job/fortrea-hiring-safety-science-analyst

13/03/2026

Syngene Hiring – Study Personnel (Senior Executive)

Leading CRDMO Syngene International is hiring Study Personnel (Senior Executive) for its GLP Bioanalytical Laboratory in Bangalore.

🎓 Eligibility: MSc Analytical Chemistry, Biotechnology, Biochemistry, Microbiology, Life Sciences, Pharmaceutical Analysis, M.Pharm Pharmaceutics / Pharmacology / Pharmaceutical Chemistry
📍 Location: Bangalore

Work on bioanalytical method development, validation, and biological sample analysis using HPLC, UPLC, LC-MS, and GC systems.

👉 Apply Now
https://pharmastuff.org/job/syngene-study-personnel-bioanalytical-laboratory

11/03/2026

Bharat Biotech Walk-In Interview | Production Roles in Vaccine Manufacturing | Hyderabad

Bharat Biotech International Limited, a leading biotechnology company known for vaccine innovation and biologics manufacturing, is conducting a Walk-In Recruitment Drive for experienced professionals in production operations.

The hiring is for candidates with expertise in injectable and vaccine manufacturing processes, including bioprocess operations, fermentation, purification, and formulation filling activities.

Department Hiring

Production – Vaccine & Biologics Manufacturing

Experience Required

3 – 10 Years

Qualification

ITI
Diploma
Graduation
Post Graduation

Candidates must have experience in injectable or vaccine manufacturing environments and should be comfortable working in shift operations.

Key Technical Areas

Drug Substance – Bioprocess

• Upstream Process
Cell Culture
Fermentation
Autoclave Operations

• Downstream Process
Virus Culture
Centrifugation
Purification
TFF (Tangential Flow Filtration)
Chromatography

Drug Product – Formulation & Filling

Formulation Operations
Filling (Vials / BFS / PFS)
C-RABS / O-RABS / Isolator Handling
Sealing & Capping
Vial Washing & Autoclave

Walk-In Interview Details

📅 Date: 14 March 2026 (Saturday)
⏰ Time: 10:00 AM – 3:00 PM

📍 Venue
Bharat Biotech International Limited
Genome Valley
Turkapally, Shamirpet
Hyderabad

Documents to Carry

• Updated Resume
• Aadhaar Card
• PAN Card
• Passport Size Photograph

This walk-in drive offers an opportunity to work with one of India’s leading biotechnology companies in vaccine and biologics manufacturing.

Apply Here: https://pharmastuff.org/job/bharat-biotech-production-bioprocess-formulation

11/03/2026

SIRO Medical Writing Hiring | Regulatory Medical Writer | Clinical Research

SIRO Medical Writing Pvt. Ltd. is currently looking for experienced professionals to join its Regulatory Medical Writing team.

This opportunity is ideal for candidates with strong experience in clinical and regulatory document preparation, scientific writing, and regulatory submission documentation.

If you have experience preparing Clinical Study Reports (CSR), Investigator Brochures (IB), Protocols, and regulatory submission documents, this role offers an excellent opportunity to work in a dynamic clinical research and regulatory environment.

Position

Regulatory Medical Writer

Experience

Minimum 5+ Years in Regulatory Medical Writing

Key Responsibilities

• Draft and review Clinical Study Reports (CSR)
• Prepare and review clinical trial protocols and amendments
• Develop Investigator Brochures (IB) and study documentation
• Write Informed Consent Documents (ICDs) and patient narratives
• Prepare tables of studies and regulatory summary documents
• Support preparation of eCTD submission documents
• Ensure regulatory documentation meets global regulatory standards

Why Join SIRO Medical Writing

• Work with a specialized regulatory medical writing team
• Exposure to global clinical trial documentation
• Opportunity to contribute to regulatory submissions and clinical research programs

How to Apply

Interested candidates can share their updated resume at:

📩Apply Here: https://pharmastuff.org/job/siro-medical-writing-regulatory-medical-writer

If you are experienced in clinical regulatory writing and scientific documentation, this could be your next career step.

11/03/2026

Hetero Healthcare Ltd Hiring | Quality Control Professionals | Assam

Hetero Healthcare Ltd is currently looking for experienced professionals to join its Quality Control (QC) team at its pharmaceutical facility in Assam.

This opportunity is ideal for candidates with experience in pharmaceutical formulation quality control, analytical testing, and regulatory compliance within manufacturing environments.

Candidates with hands-on exposure to QC laboratory practices, analytical instrumentation, and pharmaceutical quality systems are encouraged to apply.

Position

Quality Control Executive / Officer

Qualification

B.Pharm
M.Pharm

Experience

1 – 4 Years

Industry Experience Required

Pharmaceutical Formulation Manufacturing

Job Location

Assam

Key Responsibilities

• Perform analytical testing of pharmaceutical formulations
• Ensure compliance with GLP, GMP, and quality standards
• Conduct testing for raw materials, in-process samples, and finished products
• Maintain laboratory documentation and analytical records
• Support quality investigations and compliance activities

How to Apply

Interested candidates can share their updated resume at:

📩 Apply Here: https://pharmastuff.org/job/hetero-healthcare-quality-control-executive

This role offers the opportunity to grow within a leading pharmaceutical organization known for its strong presence in formulation manufacturing and healthcare solutions.

11/03/2026

USV Pharma Hiring Regulatory Affairs Executives | API, US & ROW Markets | Mumbai

USV Pharma is expanding its Regulatory Affairs team and is currently looking for experienced professionals with expertise in API regulatory documentation, global dossier submissions, and CMC regulatory activities.

These opportunities are ideal for candidates with strong exposure to DMF filings, dossier preparation, and regulatory compliance for US and ROW markets.

Open Positions

Executive – Regulatory Affairs (API)
Qualification: M.Sc
Experience: Minimum 2.5 years in API Regulatory Affairs

Key Responsibilities:
• Review regulatory documents and technical files
• Prepare and submit Drug Master Files (DMF)
• Handle CMC regulatory documentation

Executive – Regulatory Affairs (ROW Markets)
Qualification: M.Pharm
Experience: 5 years in Regulatory Affairs for ROW markets

Key Responsibilities:
• Dossier preparation and submission for ROW markets
• Handling pre-approval and post-approval regulatory activities
• Managing CMC documentation and regulatory compliance

Executive – Regulatory Affairs (US Markets)
Qualification: M.Pharm
Experience: Minimum 2 years in US Regulatory Affairs

Key Responsibilities:
• Preparation and submission of regulatory dossiers
• Handling CMC modules and documentation
• Managing pre-approval and post-approval regulatory processes

Job Location

Govandi (East), Mumbai

Work Schedule

5-Day Work Week
2nd & 4th Saturday Off

How to Apply

Interested candidates can share their updated resume at:

📩Apply Here: https://pharmastuff.org/job/usv-pharma-regulatory-affairs-executive

This is an excellent opportunity for professionals looking to grow in global regulatory affairs within the pharmaceutical industry.

11/03/2026

Aizant Hiring | IQM Executive – Bioanalytical | Hyderabad

Aizant Drug Research and Solutions Pvt. Ltd. is currently hiring experienced professionals for the role of IQM Executive (Bioanalytical) at its Hyderabad facility in Dulapally.

This position is ideal for candidates with experience in bioanalytical laboratories, internal quality monitoring systems, and regulatory compliance within clinical research environments.

The selected candidate will play a key role in maintaining quality standards, GLP compliance, and internal audit readiness within the Bioanalytical department.

Position

IQM Executive – Bioanalytical

Experience

2 – 4 Years

Qualification

M.Sc – Analytical Chemistry
B.Pharm
M.Pharm

Job Location

Dulapally, Hyderabad

Key Responsibilities

• Perform Internal Quality Monitoring (IQM) activities in the Bioanalytical department
• Ensure compliance with GLP, SOPs, and regulatory requirements
• Review bioanalytical reports, study documentation, and analytical data
• Support internal audits and quality inspections
• Maintain documentation aligned with data integrity and regulatory standards
• Coordinate with cross-functional teams to resolve quality observations

This role provides strong exposure to clinical research quality systems, bioanalytical laboratory processes, and regulatory compliance frameworks.

📩 Apply Here: https://pharmastuff.org/job/aizant-bioanalytical-iqm-executive