To review vendor evaluation & approval
To maintain R&D, ADL & Biotech related documents & review of technical documents like PDR / Technology transfer
To review documents like SOPs, BPRs, ARS, RDPs, forms, validations, qualifications & experiments and APQR for effective closure.
Assisting in preparation of audit response to customer and regulatory audits and provide response to customer queries.
Participation in internal quality audits as internal quality auditor.
Review and updation of quality system related SOPs to verify adequacy as and when required.
Review of finished products documents / dispatch documents to ensure system effectiveness.
Review and release of finished products in absence of superior
Monitoring the day-to-day activities done by QA Supervisors and Officers.
To review all quality system documentation.
To monitor production related documents for all manufacturing blocks of this site. Also to take GMP rounds at all plants for effective implementation of cGMP.