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Showing posts with the label Pharmacovigilance Jobs India 2025.

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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“Drug Safety Associate Jobs at Navatio Pharma Solutions | Pharmacovigilance Career in India”

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"Drug Safety Associate (Literature Reviewer) Jobs at Navatio Pharma Solutions – Apply Now" (Drug Safety Associate) Navatio Pharma Solutions, a renowned global Contract Research Organization (CRO) specializing in pharmacovigilance services , is inviting applications for the role of Drug Safety Associate (Literature Reviewer) . This is an excellent opportunity for professionals with 2–5 years of experience in drug safety or pharmacovigilance who are looking to advance their careers in a global environment. Job Responsibilities:- As a Drug Safety Associate – Literature Reviewer , you will be responsible for: Reviewing and processing literature cases for drug safety reporting. Ensuring compliance with international pharmacovigilance regulations (ICH, GVP, FDA, EMA). Performing case narrative writing, MedDRA coding, and ICSR submissions . Supporting global PV teams in signal detection and risk management activities. Eligibility Criteria / Qualifications:- Bachelor...

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