Ami Lifesciences is conducting a walk-in interview in Vadodara for experienced candidates in API manufacturing. The openings are for R&D, Quality Assurance and Production departments. This opportunity is suitable for candidates who want to build their career with a leading name in API manufacturing excellence and work in a world-class environment.
The walk-in is scheduled for 17th October 2026 at Ami Lifesciences’ Productivity House venue in Vadodara. Candidates should review the role-wise eligibility, skills and required documents before attending the interview.
1. R&D – CDMO, API Synthesis & Specialty Chemicals
Job Overview
The R&D role is for candidates with a chemistry background and 2 to 8 years of experience in API/CDMO and specialty chemicals. The role requires understanding of API synthesis, process development and DMF documentation.
Responsibilities
- Work on API synthesis, process development and related R&D activities.
- Support documentation and development work aligned with API specifications.
- Follow GMP, mass and IR characterization requirements.
- Work collaboratively with the R&D team for process optimisation and development.
Qualifications
- M.Sc. Organic Chemistry / Ph.D. Chemistry.
Key Skills and Experience Required
- 2 to 8 years of experience in API, CDMO and specialty chemicals.
- Basic understanding of API synthesis, process development and DMF documentation.
- Knowledge of cost-effective, quality-driven and eco-friendly processes aligned with ICH guidelines.
- Exposure to lab-scale process optimisation, product validation and technology transfer basics.
- Familiarity with KSM, intermediate and API specifications.
- Working knowledge of NMR, Mass and IR characterization.
2. Quality Assurance
Job Overview
The Quality Assurance role is for candidates with M.Sc. Organic or M.Pharm qualification and 3 to 8 years of experience in the API industry. The role focuses on cGMP, compliance, documentation, audits, change control and quality systems.
Responsibilities
- Ensure cGMP and regulatory compliance across QA operations.
- Manage AQA, IPQA, batch release, deviations, CAPA, change control and annual product quality review.
- Maintain quality documentation and ensure accurate compliance records.
- Support audit readiness and regulatory requirements.
Qualifications
- M.Sc. Organic / M.Pharm.
Key Skills and Experience Required
- 3 to 8 years of experience in the API industry.
- Hands-on experience in AQA, IPQA, batch release, deviations, CAPA, change control and audit management.
- Ability to oversee analytical data review and ensure batch adherence to data integrity principles such as ALCOA+.
- Monitor on-floor QA activities, in-process checks and documentation for accuracy and compliance.
- Maintain strong control over qualifications, preventive maintenance and calibration reviews.
- Prepare quality documents independently as per regulatory and organisational requirements.
- Drive automation, digitalisation and continuous improvement initiatives.
3. Production
Job Overview
The Production role is for candidates with B.E./B.Tech in Chemical Engineering, M.Sc. Organic Chemistry or M.Sc. Chemistry and 3 to 8 years of experience in the API industry. The role involves API production, bulk drug operations and compliance-driven production documentation.
Responsibilities
- Support API production and bulk drug manufacturing operations.
- Maintain compliance with regulatory standards and quality requirements.
- Handle batch start-up, activity monitoring and production documentation.
- Review technical documents such as batch records, SOPs, BMR, validation protocols and related records.
Qualifications
- B.E./B.Tech Chemical Engineering / M.Sc. Organic Chemistry / M.Sc. Chemistry.
Key Skills and Experience Required
- 3 to 8 years of experience in the API industry.
- Knowledge of API production and bulk drug operations.
- Ability to ensure compliance with regulatory standards for quality and efficiency.
- Experience in batch start-up, activity monitoring and calibration of balances.
- Review of technical documents including batch records, SOPs, BMR and validation protocols.
- Knowledge and exposure to cGMP is required.
Walk-In Interview Details
| Company | Ami Lifesciences |
| Venue | Productivity House, 4th Floor, BPC Road, Alkapuri, Vadodara, Gujarat 390007 |
| Date | 17th October 2026 (Saturday) |
| Time | 09:30 am to 3:00 pm |
Documents to Carry
- Updated Resume
- Educational Certificates
- Experience Certificates
How to Apply
Candidates can attend the walk-in interview at the venue on the scheduled date and time with all required documents.
Job Location: Karkhadi, Near Vadodara
Candidates unable to attend the interview can share their profiles on:
Candidates can also share their profiles on:
Note: Ami Lifesciences does not directly or indirectly charge any fees for job application, processing, training or testing. Do not participate in any such invitations.
