Candidate must have experience in API manufacturing Qualification- B.sc / M.sc Chemistry / Organic chemistry Experience - 1-4 years Candidate must have knowledge of synthesis reaction. To assist scientists in planning, performing experiments, record the process and observation on time. Follow up for analytical data and record the results on time and learn interpretation of the data with the help of seniors. To ensure the adherence to the SOPs and the safety policies of the organization. Job Types: Full-time, Permanent Pay: Up to ₹320,000.00 per year Benefits: Provident Fund Schedule: Day shift Work Location: In person
Candidate must have experience in API manufacturing Qualification - B.E Mechanical only Experience - 2-5 years in maintenance Routine maintenance tasks on production equipment and machinery according to established schedules and procedures. Preventive maintenance inspection and maintain accurate records to ensure equipment reliability. Handling of Preventive Maintenance as per Schedule and Breakdown of Equipment and Utility Equipment in consultation with Senior Engineer. Maintain the records as per SOP. To ensure Operation and Maintenance of Utilities and HVAC as per user requirement to maintain healthy condition. To maintain Engineering documentation like SOP, Qualification and Validation (HVAC and Equipment), PM Schedule, Calibration Schedule and other GMP documentation. To make sure that deviations (if any) are reported. To e aluate changes in general system, facilities and/or Equipment. To make sure that new arid when appropriate facilities and Equipment are qualified. To manage Mechanical Spares and inventory control. To ensure Safety procedures and Work Permit system for all Engineering activities. To ensure Operation and Maintenance of Purified Water System and Water System to maintain healthy condition. To maintain History Card of API, Utility and HVAC Equipment. To provide support to User department for routine activities and Job Cards in consultation with Senior Engineer. To prepare Annual Preventive Maintenance and Filter cleaning Schedule. To perform HVAC Validation and Calibration activity. To restart the required utilities and HVAC after Power failure / Power resume. Job Types: Full-time, Permanent Pay: Up to ₹216,000.00 per year Benefits: Provident Fund Schedule: Day shift Work Location: In person
Note: We required candidates who has done MSc. / BSc. Chemistry / Organic chemistry and who has experience in DMF submission for API. Experience - 5-10 years of as as RA in API manufacturing. Job Description: 1. Be the point of contact and support on regulatory matters. 2. Prepare draft for regulatory / DMF submission for API. 3. Generate, collect, compile & Review the regulatory submission documents. 4. Ensure that company product comply with the regulation of the regions where they want to distribute them. 5. Keep up to date with national and international legislation, guidelines and customer practices. Skills: 1 Excellent working proficiency in English. 2 Ability to plan, work in a dynamic and challenging environment. 3 Communication and collaboration skills. 4 Proficiency in MS office applications. 5 Data and information Management Skills Job Types: Full-time, Permanent Pay: Up to ₹600,000.00 per year Benefits: Provident Fund Schedule: Day shift Work Location: In person
Looking for a candidate who stays in nearby Ambernath and kalyan Candidate must have API manufacturing experience Experience: 4 to 10 Years Qualification: BSc. Chemistry ++ Job Responsibilities 1. To ensure that required documents available for the analysts to conduct the analysis. 2. To review of all kinds of analytical records. 3. To receive samples for analysis from Manufacturing and make entry in register. 4. To ensure analytical data generated is adequate and accurate for purpose. 5. To review RM and PM reports. 6. Executing daily activities with following safety requirement. 7. To perform analysis of Raw, Packing, Intermediate material, finished product and execute relevant documentation contemporaneously. 8. To perform analysis of hold time study samples. 9. To review all additional documents viz. AWR Log books, Protocol etc. And related raw data / electronic data. 10. To initiate change control, deviation, CAPA and incidence. 11. To involve in investigations related to all QMS elements. 12. To contribute in general upkeep of department. 13. To perform online documentation. 14. To work as per GMP/GLP in the department. 15. Any other responsibility assigned by the HOD. Job Types: Full-time, Permanent Pay: Up to ₹700,000.00 per year Benefits: Provident Fund Schedule: Day shift Work Location: In person
Looking for a candidate who who having API QA, IPQA background with minimum 1-4 year QA experience. QMS documentation is must. Qualification - B.pharma / M . pharma / B,SC chemistry Job Responsibilities 1. Document's and records issuance as per requests received from the user department as per QA SOP documents like, BMR/ BPR/ECR/SOPs/AWRs/ Protocols etc. 2. To make master documents effective and issue the controlled copies to the respective departments. 3. Retrieval and archival of documents. 4. Sampling of Raw Material and Packing material as per SOP. 5. Issuance and printing of Finished Good label. 6. Additional other activity assigned by HOD. 7. Ensure the documents are made effective then scan and word documents are saved in respective folder previous version copies of Master documents to be superseded & obsolete as applicable. 8. Strict adherence with cGMP & data integrity norms. 9. Strict adherence with safety norms. 10. Maintenance of QA Logbooks ie.Issuance logbook. To ensure document kept in document room & upkeep the document room. Job Types: Full-time, Permanent Benefits: Provident Fund Schedule: Rotational shift Work Location: In person
Note: We required only male candidates who has done MSc. /BSc. Chemistry and who has experience in DMF submission for API. Experience: 3 to 6 Years Job Description: 1. Be the point of contact and support on regulatory matters. 2. Prepare draft for regulatory / DMF submission for API. 3. Generate, collect, compile & Review the regulatory submission documents. 4. Ensure that company product comply with the regulation of the regions where they want to distribute them. 5. Keep up to date with national and international legislation, guidelines and customer practices. Skills: 1 Excellent working proficiency in English. 2 Ability to plan, work in a dynamic and challenging environment. 3 Communication and collaboration skills. 4 Proficiency in MS office applications. 5 Data and information Management Skills. Interested candidates please contact on below number. Contact: 8767919047 Job Types: Full-time, Permanent Pay: ₹300,000.00 - ₹600,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Day shift Work Location: In person Application Deadline: 10/07/2025 Expected Start Date: 27/06/2025
We are looking for Male candidate for ADL department. Candidate must have experience on HPLC and GC. candidate from nearby location is preferred. 1. To receive & register samples for analysis from R&D. 2. To analyze the samples as per instruction from Executive / Manager and as per Specification / Method of analysis. 3. To assist the Seniors during method development 4. To execute calibration of assigned Analytical instruments as per schedule. 5. To acquire training on instruments, analytical techniques and SOPs. 6. To contribute in general upkeep of department To work as per GMP/GLP in the department. Qualification - M.s c Analytical Chemistry Experience - 1-4 years in ADL Department Job Type: Full-time Pay: ₹200,000.00 - ₹350,000.00 per year Benefits: Provident Fund
As a Production Officer with API manufacturing experience in the pharmaceutical industry, you will play a key role in overseeing and managing day-to-day production activities in the API manufacturing unit. Your responsibilities will include ensuring that production processes are conducted in compliance with Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP). You will be responsible for monitoring production schedules to ensure timely completion of production targets and troubleshooting any production-related issues or deviations that may arise. Additionally, you will collaborate with quality control and quality assurance teams to maintain product quality and regulatory compliance. Maintaining accurate production records and documentation, ensuring adherence to safety and environmental regulations, and implementing process improvements to enhance efficiency and productivity will be crucial aspects of your role. You will also be responsible for training and supervising production staff, ensuring their adherence to SOPs and safety protocols. This position requires a Bachelor's or Master's degree in Chemistry (B.Sc/M.Sc) along with 1-4 years of experience in API manufacturing. The ideal candidate will possess a strong background in production processes, quality control, and regulatory compliance within the pharmaceutical industry. This is a full-time, permanent position with benefits such as Provident Fund. The work location is on a rotational shift basis, and the role will involve working in person at the assigned location.,