Quality Manager Female Graduate Jobs in Palghar

An Assistant Manager - Quality Control (QC) [Formulation] in a pharmaceutical company manages day-to-day laboratory operations, analytical testing, and compliance for drug formulations (such as tablets, capsules, liquids, or injectables) to ensure adherence to Current Good Manufacturing Practices (cGMP) and pharmacopeial standardsRequired Qualifications & Experience Education: B.Pharm / M.Pharm or M.Sc. in Chemistry / Analytical Chemistry / Biochemistry Experience: Typically 5 to 10 years of hands-on experience in a pharmaceutical formulation manufacturing or R&D setup, with at least 2-3 years in a supervisory or assistant managerial role. Technical Skills:o Hands-on proficiency in modern analytical instrumentation (HPLC, GC) and data integrity guidelines (ALCOA+). Strong knowledge of Pharmacopoeias, ICH guidelines, and stability testing Soft Skills:o Leadership, problem-solving, cross-functional communication, and audit-facing capability. Key Responsibilities Laboratory Operations & Testing:o Supervise and review testing of Raw Materials (RM), Packing Materials (PM), Water Systems (WFI/Purified Water), In-Process samples, and Finished Goods (FG) for formulation products. Ensure timely analysis using advanced analytical instruments such as HPLC, GC, UV-Vis, Dissolution Testers, FTIR, and LIMS. Compliance & Documentation:o Review and approve Certificates of Analysis (CoA), raw data, standard operating procedures (SOPs), and analytical method validation/verification (AMV) protocols. Ensure strict compliance with cGMP, GLP, and pharmacopeial standards (USP, BP, EP, IP). Investigations & CAPA:o Handle Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and laboratory incidents.

Urgent OpeningQA Manager (Veterinary Pharma)(Formulation)Veterinary Pharmaceutical Manufacturing Company.Palghar East, MaharashtraExperience 12-16 years of experience in the pharmaceutical or veterinary pharmaceutical industry. Education: B.Sc, M. ScThe QA Manager will lead the Quality Assurance function in our veterinary pharmaceutical manufacturing facility. The candidate will be responsible for ensuring compliance with GMP, regulatory requirements, quality management systems, and company policies while maintaining the highest quality standards across manufacturing operations.Key Responsibilities Manage the overall Quality Assurance function of the manufacturing plant. Ensure compliance with GMP, GLP, SOPs, and regulatory guidelines. Review and approve SOPs, Batch Manufacturing Records (BMR), Batch Packing Records (BPR), protocols, reports, and quality documents. Monitor in-process quality controls and manufacturing activities. Handle deviations, change controls, investigations, CAPA, OOS, OOT, and risk assessments. Conduct internal audits and coordinate external customer and regulatory audits. Ensure qualification and validation of equipment, utilities, and processes. Review and approve validation protocols and reports. Ensure proper documentation and data integrity practices. Coordinate with Production, QC, Warehouse, Engineering, and Regulatory Affairs to maintain quality standards. Lead vendor qualification and quality risk management activities. Train employees on GMP, GDP, SOPs, hygiene, and quality systems. Ensure timely closure of audit observations and implementation of corrective and preventive actions.

Urgent OpeningQuality Control Officer (Female)(Manufacturer of high-quality sugar-free sweeteners and nutraceuticals)Nandore, Manor Road- Palghar East, Palghar, MH Experience: 1-2 years or fresher Qualification: B. Sc (Chemistry) Working Days: Saturday to Thursday (8:30 AM - 5:00 PM) with Friday as a weekly off.------------------------------------------------------------------------------------------------------------------Job Responsibilities Ability and aptitude to contribute novel ideas and approaches in support of scientific and engineering investigations in powder processing, product formulation and functional properties of powders. Work with the formulation, quality, packaging and engineering departments. Make product samples for internal and external customers. Contribute ideas to improve process efficiency and company operations wherever possible. Maintains accurate records of work. Work with a sense of urgency and be customer-oriented. Perform any other tasks as and when assigned by the companys seniors/directors.Benefits: - PF and ESIC deductions would be there in the total salary 10 additional paid leaves are given besides regular Co. holidays 6 months would be the probation period. Employee would have to report to work on their own; The company does not provide transport

Review customer requirements Work with purchasing staff to establish quality requirements from external suppliers Set standards for quality as well as health and safety; Make sure that manufacturing or production processes meet international and national standards; Look at ways to reduce waste and increase efficiency; Define quality procedures in conjunction with operating staff; Set up and maintain controls and documentation procedures; Monitor performance by gathering relevant data and producing statistical reports; Make suggestions for changes and improvements and how to implement them; Use relevant quality tools and make sure managers and other staff understand how to improve the business; Make sure the company is working as effectively as possible to keep up with competitors; Develop quality assurance plans by conducting hazard analyses; identify critical control points and preventive measures; establishing critical limits, monitor procedures, corrective actions, and verification procedures;