* Prepare production plan as per requirement * Overall Production department activity * GMP Documentation * Make, Review, Verify SOPs & Train team as per CGMP norms * Online Completion and Reviewing of BMR/BPR * Co-ordinate with all department * Manpower management * participate with CVG/QA during validation of area * Evaluation and investigation of all market complaints and necessary corrective and preventive actions ...
* Should be well versed with Planning and Execution of Microbiological activities. * Key exposure to solid oral dosage forms (Tablet, Capsules,Oral Powder). * Should be recognized from FDA. * Male Candidates only * Excellent Communication Skill
* Candidate should have knowledge of BMR preparation & filing,FR & D Documentation,PV ,Regulatory documentation * Responsible for handling Regulatory Affairs Documentary requirements. * Experience in ROW Markets, African Countries and South East Asia * Strong knowledge of Â Regulatory documentation * Experience in Pharma Industry preferred
,confirming rework Conducting measurements test as and when required Be an active member of quality audits Conduct random inspection at manufacturing locations Responsible for overall AQL compliance at unit Qualifications B Sc/M Sc (Diploma in Quality Assurance would be preferred) or B.Pharma Experience