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Zenara Pharma, a Biophore company, has announced job opportunities for experienced pharmaceutical professionals in Regulatory Affairs and TPOA (Technical/Process Operations & Assurance). Candidates with relevant formulation experience and exposure to regulated markets are encouraged to apply.
Job Details
1. Executive – Regulatory Affairs | US & EU/ROW
- Department: Regulatory Affairs – US & EU/ROW
- Position: Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 3–4 years
- Industry: Pharmaceutical / Formulations
Key Skills & Responsibilities:
- Experience in handling US Regulatory Affairs for Finished Dosage Forms (FDFs).
- Experience in submission of ANDAs, supplements and annual reports.
- Experience in handling EU/ROW Regulatory Affairs for FDFs.
- Knowledge of dossier submissions and variations for regulated markets.
2. Sr. Manager – IPQA
- Department: IPOA
- Position: Senior Manager
- Qualification: B.Pharm / M.Pharm
- Experience: 15 years
- Industry: Pharmaceutical / Formulations
Key Skills & Requirements:
- Extensive experience in both Sterile and Oral Solid Dosage (OSD) products.
- Hands-on experience working with regulated markets such as USFDA, EMA and MHRA.
- Willingness and ability to travel to contract manufacturing sites as required.
- Strong experience in pharmaceutical manufacturing and regulated-market operations.
How to Apply
Interested and eligible candidates can share their updated CV with:
Shortlisted candidates will be contacted by the HR team.
Important Note: Only candidates with a formulation background will be considered.
Recruitment Disclaimer: Zenara has stated that it is not associated with any manpower consultancy for this recruitment.
About the Opportunity
These positions offer experienced pharmaceutical professionals an opportunity to work in areas involving global regulatory affairs, formulation products, regulated markets and pharmaceutical operations. Candidates with relevant experience in US, EU/ROW and other regulated markets should consider applying.
