Swiss, a third-generation family-owned business, leverages over 25 years of expertise in generic and specialty pharmaceuticals. Our proficiency extends to the development and manufacturing of a diverse range of sterile dosage forms. Operating globally, we export our products under our brand name, reaching over 80 countries.
Post : Executive to Asst. General Manager - Regulatory Affairs (Formulation)
Job Description
• Well versed with Dossier Preparation & Review
• Well versed with ICH and Country specific guidelines
• Can solve the MoH Deficiency response.
• Preparation & compilation of dossier in ACTD. CTD.
• Co-ordination with Quality Control. Quality Assurance and Production department tor regulatory documents.
• Timely compile documents for license renewals, update and re-registrations.
• Review of technical documents like BMR. Stability protocol & report, specification and method of analysis, process validation protocol and report required for dossier compilation.
Additional Information
Experience : 5 to 12 years
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : Ahmedabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
Interested Candidates Should walk in for an interview with a copy of latest resume, CTC Break up & Photo
Walk in Interview
Date : 4th May, 2025 (Sunday)
Time : 10 am to 4 pm
Venue : (ERIS) Shilp Accord. Opp. Times Square-2, Nr. Gwalia Bloom. Ramdas. Road. B/s. Ice-cream Library. Sindhu Bhavan.
Bodakdev, Ahmedabad-380054. Gujarat. India.
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