Chennai
INR 3.5 - 5.5 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Ensure compliance with GMP guidelines during API manufacturing processes. Monitor equipment performance and troubleshoot issues related to piping systems. Maintain accurate records of production data, quality control tests, and inventory management. Experience needed: Production - 0 -4 years Engineering production-6-8 yrs
Chennai
INR 3.0 - 8.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities: Conduct microbial testing of raw materials, in-process samples, and finished products using techniques such as BET, Sterility Testing, Media Fill, Bioburden Testing, etc. Maintain accurate records of test results and reports according to cGMP guidelines. Collaborate with cross-functional teams to resolve issues related to product quality. Operate laboratory equipment including autoclave, incubator, pH meter, spectrophotometer, microscope, etc. to conduct various analyses. Experience needed : Quality control : 1 -10 years Microbiology :5-7years
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Collaborate with cross-functional teams to resolve issues related to product development, manufacturing processes, and regulatory compliance. Ensure adherence to cGMP guidelines and company policies throughout all aspects of production chemistry operations.
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Prepare and review batch records for API production runs to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Develop and maintain knowledge of current Good Manufacturing Practices (cGMP) guidelines and industry standards.
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Develop analytical methods for pharmaceutical products using techniques such as HPLC, GC, UV-Vis Spectrophotometry, Ion Chromatography, etc. Conduct research on new analytical methodologies and technologies to improve existing methods or develop new ones. Validate analytical methods to ensure accuracy and reliability of test results. Ensure compliance with regulatory requirements and industry standards in all aspects of analytical work. Collaborate with cross-functional teams to resolve analytical issues and implement solutions.
Hyderabad
INR 3.0 - 6.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Conduct research and development activities for bulk drugs, APIs, and bulk material handling processes. Collaborate with cross-functional teams to ensure successful product launches and commercialization. Troubleshoot issues related to manufacturing processes, quality control, and regulatory compliance. Stay updated on industry trends, technologies, and regulations to drive continuous improvement initiatives.
Hyderabad, Tupran
INR 1.0 - 5.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Ensure smooth operation of production activities, including API (Active Pharmaceutical Ingredient) manufacturing, bulk drugs, and pharmaceutical production. Maintain accurate records of production data, inventory management, and batch documentation.
Hyderabad
INR 4.0 - 7.5 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Conduct quality control analysis of bulk drugs, APIs, and finished products using GC, HPLC, and other relevant techniques. Develop and maintain SOPs for laboratory operations, sampling procedures, and testing protocols. Ensure timely reporting of test results and maintain accurate records.
Hyderabad, Tupran
INR 1.0 - 2.5 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Monitor and maintain accurate records of production processes, including batch tracking and inventory management. Collaborate with cross-functional teams to resolve issues related to productivity, yield improvement, and equipment maintenance.
Hyderabad
INR 2.0 - 3.0 Lacs P.A.
Work from Office
Full Time
Roles and Responsibilities Develop and optimize organic synthesis routes to produce bulk drugs. Conduct research on new chemical compounds for pharmaceutical applications. Collaborate with cross-functional teams to design, develop, and test new products. Participate in literature searches, patent analysis, and intellectual property protection. Ensure compliance with regulatory requirements and industry standards during product development.
Nellore
INR 5.0 - 10.0 Lacs P.A.
Work from Office
Full Time
Role & responsibilities: Person skilled in analytical handling, VQ, APQR, QMS. Preferred candidate profile we have requirements 2-5 year's for Chemist and 10-12 year's for Asst. Manager. Only for male candidates.
Nellore
INR 1.0 - 5.0 Lacs P.A.
Work from Office
Full Time
Preferred candidate Profile: Only for Male candidates. Shift Incharge: 06 to 10yrs Chemist : 0yrs to 5yrs
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