Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals

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Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...

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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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