"Bristol Myers Squibb Hiring Senior Specialist – APMC Data Management in Hyderabad | Pharma Regulatory Jobs 2026"

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Bristol Myers Squibb Hiring Senior Specialist – APMC Data Management in Hyderabad (Bristol Myers Squibb Hiring Senior Specialist) Introduction The global pharmaceutical industry continues to expand rapidly, creating numerous career opportunities for professionals in regulatory affairs, quality systems, and pharmaceutical data management. One such opportunity has been announced by Bristol Myers Squibb for the position of Senior Specialist – APMC Data Management in Hyderabad, India. This role is ideal for professionals with experience in regulatory systems, pharmaceutical supply chain operations, and compliance documentation. Candidates who have worked with enterprise platforms such as Veeva Vault RIM, SAP Batch Release Hub, eCTD submissions, and regulatory documentation systems will find this position particularly suitable. Working with a globally recognized biopharmaceutical company like Bristol Myers Squibb provides exposure to international regulatory frameworks, innovative drug de...

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"Rusan Pharma Hiring Regulatory Affairs (API) in Mumbai | Pharma Jobs 2025"

"Rusan Pharma Hiring for Regulatory Affairs (API) in Mumbai | Apply Now"

(Pharma Regulatory Jobs 2025 – Mumbai)



(Rusan Pharma Hiring Regulatory Affairs (API) in Mumbai)


Rusan Pharma, a globally recognised and research-driven pharmaceutical organisation, has announced a job opening for Regulatory Affairs (API) at its Mumbai location. This opportunity is ideal for experienced regulatory professionals with strong expertise in DMF preparation, CTD/eCTD submissions, and global API regulations.

If you are passionate about regulatory compliance and want to work with an internationally approved pharmaceutical company, this role offers excellent career growth and global exposure.


About Rusan Pharma:-

Rusan Pharma is a trusted name in the pharmaceutical industry, known for innovation, compliance, and quality-driven manufacturing.
The company specialises in API, formulations, and intermediates and operates globally approved facilities at:

  • Ankleshwar

  • Dehradun

  • Kandla SEZ

✅ Approved by EUGMP, EDQM, Health Canada, and other global regulators.
✅ Head Office: Kandivali (West), Mumbai.


Key Responsibilities – Regulatory Affairs (API):-

  • Coordinate with CMC teams to compile regulatory documentation

  • Review quality & process documents for regulatory accuracy

  • Interpret and apply country-specific AMV regulatory guidelines

  • Prepare & review impurity sections of DMFs

  • Compile Drug Master Files (DMF) in CTD format

  • Submit regulatory dossiers in eCTD format

  • Handle DMF renewals, revisions, and annual updates

  • Respond to queries from global regulatory authorities

  • Ensure compliance with international regulatory standards


Required Qualifications:-

✅ Education

  • B.Pharm or M.Pharm (or equivalent discipline)

✅ Experience

  • Minimum 5 years in Regulatory Affairs (API)

  • Strong experience in DMF, CTD & eCTD submissions

✅ Skills

  • Global API regulatory knowledge (US, EU preferred)

  • Strong regulatory writing & documentation skills

  • Excellent coordination & communication abilities


Employee Benefits:-

✔ Salary: ₹6 – ₹8 LPA (based on experience)
✔ Group Mediclaim & Accident Insurance
✔ Free in-house meal facility
✔ Global regulatory exposure
✔ Weekly off: All Sundays + Alternate Saturdays
✔ Supportive & professional work environment


How to Apply:-

Interested and eligible candidates can apply via email:

๐Ÿ“ง Email: namrata.mishra@rusanpharma.com
Subject: Application for Regulatory Affairs (API) – Mumbai

๐Ÿ”— You may also apply via the official company job link (if available).


❓ FAQs:-

Q1. Experience required?
๐Ÿ‘‰ Minimum 5 years in API regulatory affairs with DMF exposure.

Q2. Job location?
๐Ÿ‘‰ Mumbai (Kandivali / nearby western suburbs).

Q3. Who should apply?
๐Ÿ‘‰ Professionals experienced in global regulatory submissions (API).



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