Posted:1 day ago|
Platform:
Work from Office
Full Time
2.To execute corporate and/or internal audits and extend support during regulatory inspections across the sites.
3.Handling document issuance and control at CQA department.
4.To review and approve the major / minor change controls across the sites and review and approve the change controls initiated by CQA or other corporate departments as applicable.
5.To prepare, review & approve the Corporate SOPs and provide training to the employees.
6.To execute, review, approve and monitor the vendor management, contract testing labs, contract manufacturing, process validation, annual product quality review, deviations, CAPA, complaints, technology transfer, quality risk management, service providers, calibration, preventive maintenance, returned goods related activities.
7.To execute the training sessions to personnel concerned on cGMP, compliance, regulatory updates and especially major findings / integrity issues detected during corporate / regulatory inspections for better awareness and minimize the repeated human errors.
8.To oversee and monitor the engineering related activities, implementation of corporate procedures and computerized systems across the sites of Cohance Lifesciences Limited.
9.To execute vendor audits/ external audits (CMU/ CTL/ Service Providers Audits).
Cohance Lifesciences
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