Chemical Manager

## Chemical ManagerApply: Pakistan - Karachi: Full time: Posted Today: End Date: October 10, 2026 (10 days left to apply): 31163026## **JOB DESCRIPTION:**Provide support to Quality Control Manager in managing QC activities related to Cleaning Validation, Computer System Validation and Annual PQR process. **Major Responsibilities:*** Prepare PQR (product Quality Review) Annual plan and implement it in timely manner.* Collect PQR related data from all stakeholders, review and analyse data and prepare PQR report.* Share PQR findings / observations / trends with respective sections and Senior Management for appropriate CAPA/recommendation.* **Cleaning Validation*** Preparation of Cleaning Validation Master Plan (CVMP), protocols and reports with worst case selection as per recent guidelines and products at site.* To ensure Cleaning Validation activities related with Products, Processes, and Equipment.* To provide support to QC in conducting glassware cleaning validation.* Conduct Cleaning validation and revalidation via preparing cleaning validation protocols, relevant documentation as per Master plan.* Perform and manage cleaning validation sampling activities along with QA support.* Revision of cleaning validation schedule as per production and supply priority as per their request and consensus.* **Computer System Validation:*** Prepare annual Computer System Validation Master Plan (CSVMP) of QC equipment and ensure adherence, prepare, and communicate monthly computer system validation plan to all stake holders.* Prepare protocols and reports of computer system validation and to perform computer system validation activity accordingly.* **General Responsibility:*** Review of applicable policies and align SOPs (related to PQR, cleaning validation, and computer system validation).* Implementation and compliance of all the SOPs and applicable policies and procedures.* To review and complete change control tasks with respect to Cleaning Validation, Computer System Validation and PQR.* To prepare impact assessment and risk assessment as or when required.* To provide support to other sections/departments with respect stability program and any data required for to PQR, Cleaning Validation, and Computer System Validation* To review AQR LL, HPR and other quality projects for assessment and actions related to above-mentioned sections.* To participate in self-inspection, Regional, Divisional and AQR Audits as an SME of above-mentioned sections.* To implement Audit CAPAs of above-mentioned sections in timely manner* Any other responsibility, assigned by Quality Control Manager or Head of Quality Assurance.* As an SME support will be provided to Stability Section when required.**Education/Knowledge & Experience:*** M.Sc. Chemistry / Pharm-D* 8-10 years’ experience in the same capacity* Knowledge of requirement for QC/QA activities, Cleaning Validation, Computer System Validation problem resolution skills and other all activities taking place in QC/QA including knowledge of Annual product quality review.* Knowledge regarding Validation and Facility etc. #J-18808-Ljbffr