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Manager (Formulation Regulatory Affairs) require at Parabolic Drugs Limited

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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)


Job Description:
Responsible for Registration dossier compilation, Product/LL site Audit, Review of documents, Handling queries, Liaisoning with regulatory agencies, record maintenance & updation of registration status.


Desired Profile:
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.

Additional Information:
Experience: 6-8 years
Location: Chandigarh

Education: B.Pharm, M.pharm
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Last Date:
12th Sept, 2011

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