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Quality Assurance Jobs at Virchow Biotech Pvt Ltd - 25 posts | M.Pharm, B.Pharm, MSc apply

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Quality Assurance Jobs at Virchow Biotech Pvt Ltd - 25 posts | M.Pharm, B.Pharm, MSc apply

VBPL is an ISO 13485:2012 and WHO – GMP certified leading global player in Biopharma sector having more than 15 years of operational experience, situated at Hyderabad. We also have offices located in USA. Innovative, ever motivated Research team and uncompromising manufacturing team in providing quality products are our strengths.

Executive (or) Sr Executive
Department : Quality Assurance
Sub-Dept : Process Validation & Equipment Validation
Vacancies : 10
Qualification : M.Tech, B.Tech M.Sc (Biotechnology, Bio Chemistry & Mechanical) ,M.Pharm B.Pharma
Budget  :  2.4 to 3.6 Lac p.a
Job Description : 1) Preparation and Execution of documents.
i) Process/Cleaning Validation activities Handling of Hold Time Studies.
ii) Review of BMR and BPR of Domestic and Export Products
2) Preparation and Execution of Different Protocol studies (Packing, Process validation, Feasibility Trial Protocol, Exhibit bath Protocol.)
3) Assisting in handling of QMS documents i.e. change control, Deviation, Incident, NCR,CAPA, Market complaint, and Product Recall.
4) Hands on experience in qualifications and validations of HVAC/Clean rooms and smoke flow studies/Air flow visualization studies.
Remarks : Exp should be between 2 to 5 years

Executive (or) Sr Executive
Department : Quality Assurance
Sub-Dept : QMS & IPQA
Vacancies : 15
Qualification : M.Tech, B.Tech M.Sc (Bio-technology, Bio Chemistry & Mechanical) ,M.Pharm B.Pharma
Budget  :  1.8 to 3.6 Lac p.a
Job Description : Handling of Change Control - Logging, Review, evaluation, Follow up, Closing, Implementation and Maintaining Documents.
Handling of Incident & Deviation - Logging, review, Follow up, Closing, Implementation and Maintaining Documents
Handling of CAPA - Review; Follow up, Closing, Implementation and Maintaining documents.
Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA
Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past
Remarks : Exp should be between 2 to 5 years

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