candidates for QC. 10. Providing resources and guidance to Managers and Executives to carry out their jobs. Setting KRAs/gols for sub-ordinates, monitoring and guide them to complete the KRAs/gols. Performance review identifying the training and development needs of all staff and fulfill it. 11. Provide
* 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
1. General Manager - QA - Site QA Head for USFDA / MHRA Approved Formulation unit 2. General Manager - QC - Site QC Head for USFDA / MHRA Approved Formulation unit Candidate should have faced USFDA / MHRA & other regulatory audits. Should have worked as a site QA / QC head for Pharma
* 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