Job Description
- Responsible for performing various IPQA oversight during the manufacturing operations, product simulation activities, campaign change activities and validations.
- Responsible for IPQA oversight of various activities of QC, Stores and Engineering departments.
- Preparation and review of the DQ, IQ, PQ and RV protocols of equipment.
- Review of the validation documents of HVAC.
- Preparation and review of the trend analysis reports.
- Review and closure of the CAPA.
- Participation in the internal audit and review of the internal audit documents.
- Assistance in the external audit.
- Document support to regulatory affairs, clinical &other departments.
- Review of BPR and Summary protocols.
- Change control review and closure.
- Preparation and review of SOP’s, STP’s, Protocols, specifications and Technical Directions.
- To prepare and review the Annual product reviews.
- Handling of Non conforming products, Expired goods, Market complaints and Recalled products
- Review of OOS/OOT and to participation in investigations
Additional Information:
Experience: 5-7 Years
Age: 28-32 years
Location: Okhla
Education: M.Pharma/ M.Sc Pharmaceutical Chemistry/ M.Sc Bio-Chemistry Industry Type: Pharma/Biotech/Vaccines
Functional Area: QA
Last Date: 10th May, 2014
Experience: 5-7 Years
Age: 28-32 years
Location: Okhla
Education: M.Pharma/ M.Sc Pharmaceutical Chemistry/ M.Sc Bio-Chemistry Industry Type: Pharma/Biotech/Vaccines
Functional Area: QA
Last Date: 10th May, 2014
Apply/Forward your Resume, okhlavfp@panaceabiotec.com
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