Job Title: Production Chemist Company: Ambrosia Remedies Pvt. Ltd. Location: Waghodia GIDC, Vadodara Experience Required: 13 Years (in pharmaceutical production) CTC: 3.5 4.5 LPA About the Company Ambrosia Remedies Pvt. Ltd. is a growing pharmaceutical company committed to manufacturing high-quality medicines while adhering to international regulatory standards. We focus on innovation, compliance, and excellence in healthcare. Job Responsibilities Carry out day-to-day production activities in accordance with SOPs and GMP guidelines. Monitor and operate production equipment for manufacturing of formulations. Ensure proper weighing, dispensing, granulation, compression, coating, and packaging processes. Maintain production records such as BMR (Batch Manufacturing Record) and BPR (Batch Packing Record). Coordinate with Quality Control (QC) and Quality Assurance (QA) teams to ensure product compliance. Maintain hygiene, safety, and discipline within the production area. Assist in process validation, scale-up, and continuous improvement initiatives. Adhere to regulatory standards (WHO, GMP) during all production operations. Key Skills & Competencies Knowledge of production processes in pharmaceutical formulations. Familiarity with GMP, GLP, and regulatory compliance. Good documentation and record-keeping abilities. Strong technical, analytical, and problem-solving skills. Team player with strong discipline and work ethics. Reach Experience in tablets and capsules production and formulation development. Approval in tablet and capsule sections from FDA is essential. Educational Qualification B.Sc. (Chemistry) / B.Pharm / M.Pharm Why Join Us? Exposure to regulated pharmaceutical manufacturing practices. Opportunity to work on end-to-end production processes. Career growth in a professional and compliance-driven environment.
Job Title: Quality Assurance Chemist Company: Ambrosia Remedies Pvt. Ltd. Location: Waghodia GIDC, Vadodara Experience Required: 13 Years CTC: 3.0 4.5 LPA About the Company Ambrosia Remedies Pvt. Ltd. is a trusted pharmaceutical company committed to ensuring the highest standards of product quality and compliance. With a strong focus on regulatory excellence, we deliver safe and effective healthcare solutions. Job Responsibilities Review and ensure compliance of batch manufacturing records (BMR) and batch packing records (BPR). Monitor in-process quality checks during production to ensure adherence to GMP guidelines. Review and approve Standard Operating Procedures (SOPs), validation protocols, and reports. Handle change controls, deviations, and CAPA (Corrective and Preventive Actions) documentation. Conduct internal audits and support external regulatory inspections. Coordinate with QC, Production, and R&D teams to maintain product quality standards. Ensure strict compliance with WHO, GMP, and GLP guidelines in all processes. Key Skills & Competencies Strong knowledge of QA processes in the pharmaceutical industry. Familiarity with documentation practices as per WHO/GMP guidelines. Good analytical, observation, and reporting skills. Ability to manage compliance and support audits effectively. Detail-oriented with strong organizational skills. Educational Qualification B.Pharm / M.Pharm Why Join Us? Exposure to regulatory audits and compliance-driven work culture. Opportunity to build expertise in Quality Assurance functions. Career growth in a structured and professional environment.
Job Title: Store Incharge Company: Ambrosia Remedies Pvt. Ltd. Location: Waghodia GIDC, Vadodara Experience Required: 25 Years (in store/warehouse management, preferably pharma or manufacturing industry) CTC: 2.5 3.25 LPA About the Company Ambrosia Remedies Pvt. Ltd. is a reputed pharmaceutical company committed to providing quality healthcare solutions with strict adherence to regulatory standards. Job Responsibilities Supervise and manage day-to-day operations of the store/warehouse. Maintain proper records of inward and outward materials, raw materials, Packing Materials and finished goods. Ensure proper storage, handling, and issuance of materials as per FIFO/FEFO. Coordinate with production, purchase, and quality teams for timely availability of materials. Monitor stock levels and conduct regular physical verification of inventory. Maintain accurate documentation, GRNs (Goods Receipt Notes), stock registers, and other records. Ensure compliance with GMP and audit requirements for material management. Optimize storage space and maintain housekeeping & safety standards in the store. Strong knowledge of computer is essential. Key Skills & Competencies Strong knowledge of store/inventory management processes. Proficiency in MS Office / ERP or inventory management software. Good documentation and record-keeping skills. Strong organizational and time management abilities. Attention to detail with problem-solving approach. Educational Qualification B.Sc. / B.Com. Why Join Us? Opportunity to work in a regulated pharmaceutical environment. Hands-on experience in store and inventory management. Career growth in a stable and reputed company.
Job Title: Quality Control Chemist Company: Ambrosia Remedies Pvt. Ltd. Location: Waghodia GIDC, Vadodara Experience Required: 13 Years CTC: 3.0 4.0 LPA About the Company Ambrosia Remedies Pvt. Ltd. is a fast-growing pharmaceutical company dedicated to delivering safe, effective, and high-quality healthcare solutions. We are committed to maintaining global quality standards while ensuring compliance with regulatory norms. Job Responsibilities Conduct quality control testing of raw materials, Packing materials, intermediates, and finished products as per defined specifications. Perform analysis using analytical instruments such as HPLC, UV, and other relevant techniques/Instruments. Monitor and test purified water, effluent water, and other utilities as per regulatory requirements. Prepare and maintain accurate documentation, analytical reports, and test records in line with WHO and GMP guidelines. Ensure adherence to Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLP). Participate in audits, validations, and continuous improvement activities in the QC department. Collaborate with production and QA teams to ensure consistent product quality. Key Skills & Competencies Proficiency in analytical techniques (HPLC, UV, Titrations, etc.). Strong knowledge of regulatory guidelines (WHO, GMP, GLP). Good documentation and reporting skills. Problem-solving mindset with attention to detail. Ability to work under timelines and in a team environment. Approval as Technical Person from FDA is preferred. Educational Qualification B.Sc. / M.Sc. in Chemistry / Pharmaceutical Chemistry / Industrial Chemistry Why Join Us? Opportunity to work with advanced analytical instruments and techniques. Exposure to international quality standards and compliance requirements. Career growth in a professional and supportive work environment.