This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To prepare, review and check all Raw material, packing material, bulk and finish product specification, method of analysis, worksheet, and COA. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Bachelor’s degree in a scientific discipline (Masters Preferred). 3-7+ years of hands on experience in the pharmaceutical industry, with specific experience in Quality Control Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹35,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): What is your notice period? What is your current salary? License/Certification: FDA certification Chemical and Physio Chemical Testing. (Preferred) Work Location: In person
This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To prepare, review and check all Raw material, packing material, bulk and finish product specification, method of analysis, worksheet, and COA. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Bachelor’s degree in a scientific discipline (Masters Preferred). 3-7+ years of hands on experience in the pharmaceutical industry, with specific experience in Quality Control Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹35,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): What is your notice period? What is your current salary? License/Certification: FDA certification Chemical and Physio Chemical Testing. (Preferred) Work Location: In person
This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To perform HPLC and Dissolution analysis. To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet. To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials. To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Experience of performing HPLC analysis. Bachelors degree in a scientific discipline (Masters Preferred). 3-7+ years of hands-on experience in the pharmaceutical industry, with specific experience in Quality Control. Job Types: Full-time, Permanent Schedule: Day shift Yearly bonus License/Certification: FDA certification Chemical and Physio Chemical Testing. (Required) Work Location: In person,
This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP approved Tablets and Capsule manufacturing facility. Specific Responsibilities: In-Process Quality Assurance (IPQA) performing checks during manufacturing, such as sampling, manufacturing, packing, and line clearance, Review and approve SOPs, Batch Records, test methods, test results, labeling materials, specifications, analytical validation protocols and reports, stability protocols and reports. Review and approve records, including associated change controls, investigations (deviations, out-of-specification/out-of-trend), and analytical data. Understand and able to interpret regulatory authority regulations, guidelines and policies. Qualifications / Requirements: Bachelor’s degree in a scientific discipline (Masters Preferred). 2+ years of hands on experience in the pharmaceutical industry, with specific experience in GMP Quality Assurance Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Experience: Manufacturing: 1 year (Required) License/Certification: FDCA approval in Tablets/Capsule Production (Preferred) Work Location: In person
This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP approved Tablets and Capsule manufacturing facility. Specific Responsibilities: In-Process Quality Assurance (IPQA) performing checks during manufacturing, such as sampling, manufacturing, packing, and line clearance, Review and approve SOPs, Batch Records, test methods, test results, labeling materials, specifications, analytical validation protocols and reports, stability protocols and reports. Review and approve records, including associated change controls, investigations (deviations, out-of-specification/out-of-trend), and analytical data. Understand and able to interpret regulatory authority regulations, guidelines and policies. Qualifications / Requirements: Bachelor’s degree in a scientific discipline (Masters Preferred). 2+ years of hands on experience in the pharmaceutical industry, with specific experience in GMP Quality Assurance Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Experience: Manufacturing: 1 year (Required) License/Certification: FDCA approval in Tablets/Capsule Production (Preferred) Work Location: In person
As the Quality Control Operations Manager in a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility, your role involves the following responsibilities: - Performing HPLC and Dissolution analysis. - Reviewing and checking all Raw material, packing material, bulk and finish product specification, method of analysis, and all worksheets. - Reviewing and checking Different validation protocols like process, cleaning, analytical method. - Reviewing and checking Stability study and hold time study protocols. - Ensuring timely sampling and analysis of incoming materials, such as raw materials and packing materials. - Ensuring timely analysis of bulk, finish product, stability sample, and validation sample. Qualifications and Requirements: - Experience in performing HPLC analysis. - Bachelors degree in a scientific discipline (Masters Preferred). - 3-7+ years of hands-on experience in the pharmaceutical industry, with specific experience in Quality Control. In addition to the specific responsibilities and qualifications, the company offers a full-time, permanent job type with day shift schedule and a yearly bonus. A FDA certification in Chemical and Physio Chemical Testing is required for this position. The work location is in person.,
FDA approval in the tablet and capsule section is highly appreciated; Minimum 5 years of hands-on production experience Knowledge of various types of equipment of granulation, compression, coating, and capsule filling; Review Standard operating procedure of manufacturing equipment and process; Execute qualification process and validation process of equipments and products; Prepare/review batch manufacturing records; and Handle and review change control, deviation, risk assessment, CAPA for various manufacturing activities. Job Type: Full-time Pay: ₹55,000.00 - ₹85,000.00 per month Experience: total work: 5 years (Required) License/Certification: FDA approval (Required) Work Location: In person