Manager (Formulation Regulatory Affairs) require at Parabolic Drugs Limited
Parabolic Drugs Limited is one of the fast growing API (Active Pharmaceutical Ingredients) and API intermediate manufacturing and marketing company in the SME segment, with increasing international presence and a strong R&D foundation, based at Chandigarh, India. Commissioned in 1998, PDL has two fully functional, state of the art manufacturing units, a WHO-GMP certified Unit based in Derabassi (Punjab) and a world class Semi Synthetic Penicillin manufacturing plant at Panchkula, (Haryana) with one of its products been approved for sales to USA, respectively.
Post: Manager (Formulation Regulatory Affairs)
Responsible for Registration dossier compilation, Product/LL site Audit, Review of documents, Handling queries, Liaisoning with regulatory agencies, record maintenance & updation of registration status.
B.Pharma or M.Pharma with International Regulatory Affairs exposure in reputed pharmaceutical companies for Asean, African, Latin American & CIS regions, Sound knowledge of ICH guidlines, Knowledge of formulation QA & QC will added advantage.
Experience: 6-8 years
Education: B.Pharm, M.pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Last Date: 12th Sept, 2011
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