B.E

Experience into Complex Injectable and Complex Equipment like HPH, Isolator, Wet Mill, ANFD. Experience in injectable and Ophthalmic dosage form like suspension & Gel forming and simple ophthalmic range.

Strong knowledge of GMP, GDP, and regulatory compliance for pharmaceutical warehousing. Exposure of various instruments/ software like empower 3, LIMS and other software.

BPharm or Post Graduate Degree in Basic, Allied Sciences Biotechnology, Biochemistry, Chemistry, Material Science, Environment Science, Any discipline of Life Sciences OR Graduate, Post Graduate Degree in Professional Course.

1st Class M.Sc, Masters degree in related discipline life sciences, Genetics, Biotechnology with 2 years research experience.

Finished, AMV & Stability Section, knowledge of Instrument - HPLC, GC, Preferably know-how of Chromeleon Software.  Good exposure require in IPQA - OSD & Sterile, Qualification OSD & Sterile & Documentation Cell

Masters, Integrated Masters Degree in Pharmaceutical Sciences or Natural or Agricultural OR bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent.

Masters, Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences MVSc, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent

He, she participates in all activities relating to preparation, submission and follow up to obtain approvals, renewals for products and its variations and line extension indications and labeling approvals of medical devices of various business units of Medtronic. He, she will be responsible for providing technical support by interpreting federal and local regulations as they apply to products, processes, practices and procedures

M.Pharm, B.Pharm, M.Sc, B.Sc. Functional experience in Calibration, Instrumentation, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities. Through knowledge on cGMP norms & Laboratory safety