Manufacturing Chemist Job Vacancies in Maharashtra

Key Responsibilities:Implement and monitor QA systems (as per GMP/ISO/FDA guidelines).Conduct internal audits and support external audits (regulatory & client).Review and approve SOPs, batch records, and quality documents.Investigate and document deviations, CAPA, OOS, and change controls.Coordinate with production, QC, and regulatory teams for compliance.Ensure training and qualification of QA team members.Maintain records and documentation per regulatory standards.

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.

Job Title: Production/Manufacturing Chemist - Pharma IndustryJob Overview:We are seeking a highly skilled and motivated Production/Manufacturing Chemist to join our pharmaceutical manufacturing team. The successful candidate will play a key role in the production process, ensuring the efficient and compliant manufacturing of pharmaceutical products. This position requires a strong background in chemistry, a keen attention to detail, and a commitment to maintaining high-quality standards.Responsibilities:Production Planning and Execution:Collaborate with the production planning team to develop and implement production schedules.Execute production processes according to established protocols, ensuring timely completion and adherence to quality standards.Batch Record Review and Documentation:Review and approve batch records for accuracy and compliance with standard operating procedures (SOPs).Maintain detailed and accurate production documentation.Quality Assurance:Work closely with the quality control team to ensure product quality and compliance with regulatory requirements.Implement corrective and preventive actions as needed to address deviations from quality standards.Equipment Operation and Maintenance:Operate manufacturing equipment and machinery in accordance with safety guidelines and SOPs.Perform routine maintenance and calibration of equipment to ensure optimal performance.Process Optimization:Continuously evaluate and improve manufacturing processes to enhance efficiency and reduce costs.Collaborate with the research and development team to scale up new processes for commercial production.Compliance and Regulatory Affairs:Stay informed about industry regulations and ensure compliance with current Good Manufacturing Practices (cGMP) and other relevant standards.Support regulatory inspections and audits as needed.Team Collaboration:Work collaboratively with cross-functional teams, including research and development,

We have vacant of 01 Assistant Manufacturing Chemist Job in Raigad, Experience Required : 1 Year Educational Qualification : B.Sc Skill Candidates with Bsc chemistry, Candidates with Bsc chemistry etc.

Equipment handling:Operation and Cleaning of Equipments used in the process area.Trouble shooting of the equipments during process.Production PlanningManufacturing and packing of the products as per BMR / BPR.Material HandlingConsumption of Raw and packing material and solvents in shop floor.Safety, health and environment:On line monitoring of the environment conditions in process area.Desired Certifications: cGMP certificates, Ms Office, SAP preferredFunctional Skills:Handling of unit operations and unit process.Documentation capabilities like filling of BMR / BPR/ECR etc.Knowledge of basic cGMPCritical thinkerProblem solving attitudeAttention to detailsHandling manpower in Shop-floorPlanning of day to day activity

A. COORDINATION OF MANUFACTURING SITES FOR TABLETS, CAPSULES, OINTMENT AND INJECTIONS.. IPQC- VERIFICATION OF PARAMETERS ON SITE. B. FOR QUALITY ASSURANCE/QC- REGULATORY AFFARIS - FOR REGISTRATION OF PRODUCTS IN FOREIGN COUNTRY. PREPARATION OF ECTD AS PER FORMAT. VERFICATION OF QUALITY OF PRODUCTS, REPLYING TO QUERY FROM REGULATORY AUTHORITIES FROM FOREIGN AGENCY.