| Job Code | : JN/42610/2013 |
|---|---|
| Contact Person | : Sharmila.M |
| Industry type | : Pharmaceutical |
| Position | : Manager - QA |
| Work Experience | : 8 to 12 |
| Status | : active |
| Response Ph/Mob | : 44 45110015/19 |
| Response Email 1 | : sharmila@busisol.net |
| Date | : 16-Feb-2018 |
| End Date | : 16-Mar-2018 |
| CTC Range | : 9LPA |
| Posted by | : |
| : | |
| Job description | : • Candidate shall be experienced in handling different dosage forms viz. Tablets, Capsules, Ointment, Liquid dosage forms etc. • Must be conversant with different Regulatory guidelines and GMP requirements. • Must be experienced in preparation, approval and execution of validation documents and GMP documents. • Must be able to handle day to day QA activities and Quality issues that may come up during routine production work. • Experience in handling the site at Project stage will be an added advantage. • Must have exposure to handling different regulatory audits. • Must be conversant will Quality Management System principles and implementation of the same. • Previous experience of handling a team will be an added advantage. • Handling of country audits. • Not less than 10 years of experience in Pharmaceutical Industry. • Conversant with local and international regulatory Guidelines and GMP requirements. • Candidate should be FDA approved and experienced in liasoning with FDA |
| Uploaded Date | : 16-Feb-2018 |
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