opening for the post  Officer to Senior Executive in Vaccines QC at Zydus Lifesciences

opening for the post  Officer to Senior Executive in Vaccines QC at Zydus Lifesciences

 

Inviting candidates for the post of Officer to Senior Executive in Vaccines QC for Vaccine Technology Centre, Ahmedabad

Seeking candidates for Vaccines QC related to Bacterial, Recombinant and Viral Vaccine products.

Officer to Senior Executive
M.Sc. in Biotechnology / Microbiology with 5-7 years of experience in technical work in bacterial and viral vaccine in-process, DS & DP testing, release and stability, should be well versed with biochemical assays (protein, o-acetyl) immuno-chemical assays, cell-based assays, virus titration, RT-PCR and electrophoresis, should have instrumental knowledge on pH meter, analytical balance, UV-spectrophotometer, karl fischer, real time PCR, multimode plate reader and ELISA.

Candidates should also have knowledge on calibration and qualification of equipment and instruments and experience in preparing SOPs, specifications, STPs, study protocols, handling stability studies and maintaining records. They would be responsible in performing / monitoring activities in compliance with GMP / GLP / GDP and record keeping, preparing method validation protocol, executing method validation, coordinating with engineering / maintenance department or third-party labs as and when required and should possess basic skills in MS-Office, LIMS and SAP.

Candidate Profile
• The candidate should possess 5 to 7 years of technical work experience in Bacterial and viral vaccine In-Process, DS & DP testing, release & stability.
• Shall be well versed with Biochemical assays (Protein, O-acetyl) immuno-chemical assays, Cell based assays, Virus titration, RT-PCR and electrophoresis,
• Instrument knowledge on pH meter, Analytical balance, UV-Spectrophotometer, Karl Fischer, Real time PCR, Multimode plate reader and ELISA.
• Knowledge in calibration and qualification of equipment and instruments.
• To perform/ monitor activities in compliance with GMP/GLP/GDP and record keeping.
• Experience in preparing SOPs, Specification, STPs and Study protocols
• To prepare method validation protocol and execute method validation.
• Experience in handling stability studies and maintaining records.
• Role shall require to coordinate with engineering/ maintenance department or third party labs as and when required.
• Should possess basic skills in MS-Office, LIMS & SAP

Additional Information
Experience : 5 to 7 years
Qualification : M.Sc. in Biotechnology / Microbiology
Location : Ahmedabad, Gujarat
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : QC
End Date : 31st August 2023

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Job Category: pharma
Job Type: Full Time
Job Location: Ahmedabad

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Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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