"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Top Pharma Job: Regulatory Affairs Openings at Hetero Hyderabad"

"Hetero Pharma Hiring Regulatory Affairs Specialists in Hyderabad – Apply Now"


Are you a skilled professional in Regulatory Affairs (RA) looking to boost your career with a globally recognized pharmaceutical company? Hetero, one of India’s leading pharma organizations in formulations and APIs, is inviting applications for Regulatory Affairs Specialist positions at its Jeedimetla, Hyderabad facility.

This is a golden opportunity for professionals with expertise in ANDA, CMC, MAA submissions, lifecycle management, and regulatory compliance to join a company with strong global presence.


Job Responsibilities:-

As a Regulatory Affairs Specialist at Hetero, you will be responsible for:

  • Reviewing, compiling, and submitting Abbreviated New Drug Applications (ANDA).
  • Managing Life Cycle Management (LCM) of pharmaceutical formulations.
  • Handling pre-approval and post-approval submissions.
  • Preparing and supporting Marketing Authorization Applications (MAA) for multiple global markets.
  • Ensuring compliance through CMC documentation and regulatory variations.

Required Qualifications & Experience:-

To be eligible, candidates must have:

  • Education: M.Pharm / B.Pharm / M.Sc in Pharmaceutical Sciences or a related field.
  • Experience: 3 to 9 years in Regulatory Affairs (Formulations – Emerging and ROW markets).
  • Strong understanding of CMC, global regulatory submissions, and documentation.
  • Practical exposure to regulatory submissions and lifecycle management.

Why Choose Hetero?

Joining Hetero means being part of a global pharmaceutical leader with diverse opportunities. Key benefits include:

  • Working with one of India’s top pharmaceutical companies.
  • Gaining international exposure across regulatory markets.
  • Professional growth in the Regulatory Affairs domain.
  • Competitive salary along with performance-based benefits.

How to Apply:-

Interested candidates can share their CVs directly to the recruiter:

📧 Email: chandrasekhar.r@hetero.com
Subject Line: Application For RA


FAQs:-

Q: What is the role being offered at Hetero?
A: The opening is for Regulatory Affairs Specialists at the Jeedimetla, Hyderabad facility.

Q: What is the required experience for this job?
A: Applicants should have 3 to 9 years of experience in Regulatory Affairs (Formulations).


✨ Don’t miss this opportunity to accelerate your career in Regulatory Affairs with Hetero Pharma. Apply today and take the next step toward professional growth in the global pharmaceutical industry.

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