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

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

Preferred candidate Profile: Only for Male candidates. Shift Incharge: 06 to 10yrs Chemist : 0yrs to 5yrs

Roles and Responsibilities Ensure compliance with GMP guidelines during API manufacturing processes. Operate centrifuges, reactors, and other equipment safely and efficiently. Maintain clean room design principles to prevent contamination. Monitor bulk drug production lines for quality control purposes. Collaborate with team members to achieve production targets.

Roles and Responsibilities Only for male candidates Department requirements - Production, solvent recovery plant, Technical service dept, Warehouse, Quality assurance, Quality control, R&D, AR&D, DQA, RA and HR Ensure compliance with GMP guidelines and regulatory requirements for API manufacturing. Oversee bulk drug production, quality control, and warehousing operations. Develop and implement effective QA/QC procedures to ensure product quality and purity. Collaborate with cross-functional teams to resolve issues related to active pharmaceutical ingredients (APIs) and bulk drugs. Conduct regular audits and inspections to maintain high standards of quality assurance.

Roles and Responsibilities ONLY FOR MALE CANDIDATES. Conduct quality control tests on OSD products to ensure compliance with regulatory requirements. Perform IPQA activities such as inspection, sampling, and testing of raw materials, intermediates, and finished goods. Ensure adherence to cGMP guidelines during formulation development and manufacturing processes.

Roles and Responsibilities: ONLY FOR MALE CANDIDATES Conduct quality assurance activities such as BPR review, BMR review, SOP preparation, validation, cleaning validation, equipment qualification, process validation, stability analysis, and OOS/OOT investigations. Ensure compliance with regulatory requirements by maintaining records of batch manufacturing, testing results, and other relevant documents. Develop and implement quality control procedures for bulk drugs production. Perform analytical testing of APIs using HPLC/GC techniques.

Roles and Responsibilities ONLY FOR MALE CANDIDATES Prepare and review batch records for API production runs. Collaborate with cross-functional teams to resolve issues related to product development and manufacturing. Maintain accurate records of test results, inventory management, and equipment maintenance.

Role & responsibilities : Only for male candidates Shri Kartikeya Pharma [Jadcherla / India] located in JADCHERLA TELANGANA, India had its last known inspection on 04 Jan 2024. There are 1 known inspections on record Preferred candidate profile Freshers,1-2 yrs

Role & responsibilities : Only for Men Development, Synthesis & Manufacturing of Pharmaceutical Intermediates and Active Pharmaceutical Ingredients,Research. Preferred candidate profile 2YRS TO 5YRS EXPERIENCE MALE CANDIDATES