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Neuland LaboratoriesLtd : Deputy Manager - Regulatory Affairs (30/09/2008)
We at Nueuland have been in the forefront of aiding and accelerating drug development and the manufacturing process since the past twenty five years. The company derives its core strength from a deep understanding of complex chemistry and an insight into the drug development process. The Company has two SFDA and EDQM complaint manufacturing sites professionals, dedicated to the cause of improving global health care. Currently, we are looking for qualified individuals for the following positions:Roles and Responsibilities: Review and submission of Drug Master Files, Technical Data Packages, compilation of updates of different Active Pharmaceutical Ingredients (API's) for filling purpose to Regulatory Authorities of various countries as per global regulatory guidelines.Compilation of responses to customer / regulatory deficiencies for various Active Pharmaceutical Ingredients. Expected Profile: Masters (full-time) in Chemistry with 5 to 7 years of hands-on experience in Regulatory Affairs with API manufacturing companies. Should have lead a fair-sized team of Graduates and Post-graduates. Should be able to work independently. Must possess computer as well as communication skills. PhDs with relevant experience may also apply. Qualified candidates with lesser experience can also apply and would be considered for other suitable position.
Interested candidates can forward their updated profiles addressed to Sr Manager - Human Resources or email them to email@example.com mentioning the position applied for in the subject line of the email. All the positions above are based at Hyderabad.
Manager-Human Resources, Neuland Laboratories Limited, 204, Meridian Plaza, Ameerpet, Hyderabad 500016. Email: firstname.lastname@example.org
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