AMI Lifesciences, a rapidly expanding and professionally managed organization recognized for its strong presence and market leadership in the Domestic and International API (Active Pharmaceutical Ingredient) manufacturing sector, is hosting a large-scale walk-in interview event. This is an exceptional opportunity for experienced professionals in the pharmaceutical industry to join their team in Gujarat.
The organization is seeking dynamic and skilled candidates for key positions across its Production, Quality Assurance (QA), and Quality Control (QC) departments at its Korakhadi facility, near Vadodara.
Open Positions and Eligibility Details
Candidates must meet the specific educational and experience criteria for each department:
1. Production Department
Criteria
Details
Eligibility
B.Tech Chemical / M.Sc. Chemistry
Experience
2 to 7 years in the API Industry
Key Skills Required
Expertise in API Production and Bulk Drug manufacturing. Must ensure compliance with all regulatory standards for efficiency and quality. Responsibilities include Batch start-up activity, process monitoring, balance calibration, and thorough review of technical documents like SOPs, BMRs (Batch Manufacturing Records), and validation protocols. Comprehensive knowledge and exposure to cGMP (current Good Manufacturing Practices) is mandatory.
2. Quality Assurance (QA) Department
Criteria
Details
Eligibility
M.Sc. Organic Chemistry / M.Pharma
Experience
4 to 12 years in the API Industry
Key Skills Required
Ensuring strict cGMP and regulatory compliance across all QA operations. Core duties involve managing AQA (Analytical Quality Assurance), IPQA (In-Process Quality Assurance), batch release, and critical quality events like deviations, CAPA (Corrective and Preventive Actions), and change control. Candidates must oversee analytical data review and strictly enforce ALCOA+ data integrity principles. The role also involves monitoring on-floor QA activities, documentation accuracy, and maintaining control over qualifications, preventive maintenance, and calibration reviews. Driving automation and continuous improvement initiatives is a plus.
3. Quality Control (QC) Department
Criteria
Details
Eligibility
M.Sc. Organic / Analytical Chemistry / M.Pharma
Experience
2 to 5 years in the API Industry
Key Skills Required
Proficiency in operating analytical instruments, including HPLC, GC, and performing wet chemical analyses on raw materials, intermediates, and finished products. Key responsibilities include the preparation of SOPs (Standard Operating Procedures), conducting stability analysis, and testing market samples as per regulations. Must maintain GLP (Good Laboratory Practice)-compliant documentation and audit-ready records, and be proficient in operating multiple laboratory software platforms for testing and reporting.
Pharm'Up 
