Job Description

Master in Pharmacy with 7-9 years of experience in API industry with related experience in the following fields: QA, Manufacturing, Training & GMP Technical skills & Competencies / Language Knowledge of cGMP & Regulatory Guidelines Modern HR Techniques Communication Analytical Ability Listening Public Speaking KEY ACCOUNTABILITIES Quality Management/Continuous Improvement Management and control of SOPs, Master documents, labels & other GMP impacted documents. Implementing necessary quality systems at the site including complaint Investigation, qualification and validation, change control, deviation and non-compliance management, documentation, supplier quality assurance etc. Out of specification & Out of trend investigation. Deviation Investigation. Incidence investigation. Review of Batch Manufacturing Records (BMRs), Analytical record & related documentation. Validation & Qualification. Change control review & management. Preparing the Annual Product Review and Annual Quality Review. Batch Rework/Reprocessing Approval. Approval of repacking, relabeling and non-standard batch size procedures as per applicable SOPs. Release/ rejection API & Intermediate. Conducting training program. Reviewing stability program. Review of Analytical method validation and qualification documents of Analytical instruments. Review of Equipment cleaning Records (ECRs). Issuance of all related GMP document. Compliance Ensure adherence to Corporate Quality Directives, Local FDA regulations by Knowing the requirements Performing Gap analysis and making a compliance plan for closure of gaps Audit trail review Supporting Regulatory Affairs in related documentation. Prepare for and attend to external / regulatory quality audits. Review of calibration and preventive maintenance program. Review of work orders. GMP round in plant. Validation: Review of validation plans, protocols and reports. Review of qualification plans, protocols and reports. Documentation Control: Preparations of quality system SOPs. Review of other departmental SOPs. To ensure controlled distribution and archival of documents and records. Control changes in master documents and records through change control procedure. Assuring quality of products by Ensuring compliance with applicable SOPs Management of deviation/failure investigations By controlling the changes made to facility / equipment / product / process and master documents and records by following change control procedure Investigation of customer complaints By ensuring implementation of corrective and preventive actions proposed in deviation/failure investigations, audit / inspection compliance, and customer complaint investigations. Training : To develop cGMP training modules and impart training. Coordination QC (Pharmaceuticals-Ankleshwar): For testing of water for microbiological attributes, environmental monitoring, stability program & local regulatory compliance. HR&A for training activity API-II (Production): For co-ordination of QA related activities Purchase (Mumbai and Ankleshwar): For co-ordination of supplier QA activities IS - Ensure IS compliance in coordination with IS experts. Other Coordinating with various agencies for making of the quality agreements. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations. To support PD (Pharmaceutical Development) and supplier quality assurance activity as needed. Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.

foundit