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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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"

"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"



(ProPharma Hiring Pharmacovigilance)



Are you passionate about drug safety and pharmacovigilance? ProPharma, a trusted global leader in regulatory sciences, clinical research, and drug safety, is inviting applications for the Pharmacovigilance Safety Scientist role in India. This position offers an excellent opportunity to work on global projects and contribute to improving patient safety worldwide.


Key Responsibilities:-

As a Pharmacovigilance Safety Scientist at ProPharma, you will be responsible for:

  • Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR.
  • Developing and maintaining Risk Management Plans (RMPs).
  • Preparing Signal Management Reports and conducting literature searches.
  • Reconciling process trackers and validating extracted data.
  • Generating and reviewing line listings from safety databases.
  • Supporting ad-hoc pharmacovigilance activities as per project requirements.
  • Ensuring all deliverables meet ICH-GCP, FDA, EMA, and global PV regulations.
  • Contributing to SOPs, deviations, and CAPA activities.
  • Analyzing large volumes of safety data with precision and accuracy.


Required Qualifications & Skills:-

  • Education: Bachelor’s/Master’s in Pharmacy, Nursing, Life Sciences, or related health sciences.
  • Experience: Minimum 2+ years in pharmacovigilance, with expertise in medical writing, signal detection, or literature review.
  • Strong understanding of global PV regulations.
  • Excellent communication, writing, and analytical skills.
  • Proficiency in MS Office tools and PV database applications.
  • Ability to work in a matrix and multicultural environment.


Why Join ProPharma?

  • Be part of a global leader in pharmacovigilance and regulatory sciences.
  • Contribute to patient safety and global healthcare improvement.
  • Opportunity to work with a collaborative, diverse, and inclusive team.
  • Strong career growth in drug safety, PV, and medical writing.


How to Apply:-

Interested candidates can apply directly through the official link below:

๐Ÿ‘‰ Apply Here – Pharmacovigilance Safety Scientist at ProPharma India


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