You are hereOpenings in Regulatory Affairs, Formulations/Production, QA, QC in Nectar Lifesciences | Invites M.Pharm, B.Pharm, B.Sc, M.Sc, Ph.D
Openings in Regulatory Affairs, Formulations/Production, QA, QC in Nectar Lifesciences | Invites M.Pharm, B.Pharm, B.Sc, M.Sc, Ph.D
Nectar Lifesciences Ltd., Chandigarh, India a US$ 200 million company engaged in the business of manufacturing & marketing products in lifesciences particularly Antibacterial I.e. Cephalosporins with 40% market share in API's I.e. 3rd & 4th generation Cephalosporins out of India.
We are a knowledge driven organization which constitutes a vital part of fast growing Indian Pharmaceutical Industry. In a short span of existence, Nectar has today emerged as 365 ranked organization amongst the top 500 Indian Corporates & is currently among top 25 fore runners of the Indian Pharmaceutical industry with a top 5 ranking in the Indian Bulk Drug Industry from a stand alone Active Pharmaceutical Ingredients (API Manufacture) perspective.
In order to meet massive expansion programme we require following personnel in the related field:
DGM / AGM / Sr.Manager / Manager - Regulatory Affairs (Formulations)
Desired Profile: M.Pharm/Ph.D with 08 -15 years of experience in Regulatory Affairs in reputed pharmaceutical companies of which 6-9 years must be in handling regulatory affairs for US/EUI Canada. Must have working knowledge of electronic submissions (eCTD/SPL etc.).
Asst.Manager / Sr. Executive (US/EU) Regulatory Affairs
(Formulations) — Desired Profile : Having 4-6 years of experience in the handling of BA/BE studies - protocol and study reports review, study monitoring, auditing of CRO sites and data. Medical writing and Pharmacovigilance would be an added advantage. Good communication skills. Travelling within India would be involved.
Executive (US) Regulatory Affairs (Formulations)
Desired Profile: Having 1 -2 years of experience in Labeling section/ SPL of ANDAs and eCTD for various dosage forms.
Research & Development - Desired Profile : M.Pharm/Ph.D with the experience of 10 - 18 years. The candidate should be well versed with Regulatory guidelines, US-FDA, UK-MHRA and ANDA preparations. The candidate should have hands on experience in Product development, development of new products, improving the existing product formulations.
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