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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“Accenture Hiring B.Pharm & M.Pharm Graduates for Pharmacovigilance Services Associate Role in Bengaluru”

"Accenture Hiring Pharmacovigilance Services Associates in Bengaluru – Apply Now"

(Accenture Hiring)

Accenture, a global leader in professional services, is inviting applications for the role of Pharmacovigilance Services Associate in Bengaluru. This opportunity is ideal for B.Pharm and M.Pharm graduates who are looking to build a strong career in drug safety, pharmacovigilance, and regulatory compliance.

Job Role and Responsibilities:-

As a Pharmacovigilance Services Associate at Accenture, you will be responsible for:

  • Managing affiliate mailboxes and reconciling safety reports.
  • Conducting follow-ups for both serious and non-serious adverse events.
  • Performing case identification, MedDRA coding, and case processing.
  • Submitting and tracking Individual Case Safety Reports (ICSRs) in line with global regulations.
  • Collaborating with supervisors and team members to resolve queries.
  • Working in rotational shifts as per business needs.

Eligibility Criteria:-

To apply for this position, candidates must have:

  • Qualification: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).
  • Experience: 1–3 years in pharmacovigilance, drug safety, or clinical research.
  • Skills Required: Knowledge of MedDRA coding, ICSR processing, safety case management, and regulatory compliance.

Why Join Accenture?

Accenture offers:

  • Exposure to global biopharma projects and regulatory operations.
  • Training and professional growth in drug safety and pharmacovigilance services.
  • A diverse and inclusive work environment with employee well-being initiatives.
  • Career advancement opportunities in the life sciences and healthcare industry.

How to Apply:-

Interested candidates can apply directly through the official Accenture careers portal:
👉 Apply Here – Accenture Pharmacovigilance Services Associate


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