India's DMPLOI - Jobs & Networking AppAmi Drugs Pvt. Ltd., a well-established API pharmaceutical manufacturing company, has announced a Walk-In Interview Drive for experienced professionals in Quality Control (QC) and Environment, Health & Safety (EHS) departments. The recruitment drive is scheduled for 12th June 2026 (Friday) at the company’s manufacturing facility in Bavla, Ahmedabad, Gujarat.
This hiring initiative offers excellent career opportunities for candidates with relevant experience in the API and pharmaceutical industry who are looking to advance their careers in quality assurance, analytical chemistry, safety management, and environmental operations.
About Ami Drugs Pvt. Ltd.
Ami Drugs Pvt. Ltd. is a reputed pharmaceutical API manufacturer known for maintaining high standards of quality, safety, and regulatory compliance. The company focuses on cGMP-compliant manufacturing practices and continuously seeks skilled professionals to strengthen its operational excellence.
Available Positions
1. Quality Control (Chemist to Officer)
Qualification:
M.Sc. in Organic Chemistry / Analytical Chemistry
M.Pharm
Experience:
3 to 7 years in the API industry
Key Skills:
Hands-on experience with GC and HPLC operations
Wet analysis and stability testing
cGMP documentation practices
Method validation and instrument qualification
OOS/OOT investigations
Regulatory compliance activities
2. EHS (Safety Executive)
Qualification:
M.Sc. Environmental Science + PDIS
Experience:
5 to 10 years in the API industry
Key Responsibilities:
Ensure cGMP and regulatory compliance
Handle deviations, CAPA, audits, and change controls
Analytical data review and ALCOA+ compliance
On-floor QA monitoring and documentation review
Qualification, calibration, and preventive maintenance oversight
3. EHS (MEE / ETP Operator)
Qualification:
ITI AOCP
Experience:
2 to 5 years in API/Pharma Industry
Key Responsibilities:
EHS regulatory compliance
Safety inspections and risk assessments
Permit-to-work system management
PPE compliance monitoring
Safety training and awareness programs
Maintenance of statutory and compliance records
Coordination with production and engineering teams
Walk-In Interview Details
Interview Date: 12th June 2026 (Friday)
Time: 10:30 AM to 4:00 PM
Venue: Ami Drugs Pvt. Ltd.
Survey No. 748 (2),
Bavla–Adroda Road,
Adroda Village, Ta. Bavla,
Dist. Ahmedabad – 382220, Gujarat
Job Location: Bavla (Near Ahmedabad)
Email for Profile Submission: careers@amidrugs.com
Candidates who are unable to attend the walk-in interview may share their updated profiles through the above email address.
Important Notes
Ami Drugs does not charge any fee for recruitment, processing, training, or testing.
Candidates should be 18 years or older.
Applicants should carry updated resumes, educational certificates, experience documents, and identification proof.
Why Join Ami Drugs?
Opportunity to work in a regulated API manufacturing environment.
Exposure to advanced analytical instruments and quality systems.
Career growth in QC and EHS functions.
Strong focus on compliance, safety, and professional development.
Technical FAQs
1. What is the role of HPLC in pharmaceutical Quality Control?
HPLC (High-Performance Liquid Chromatography) is used to identify, quantify, and verify the purity of active pharmaceutical ingredients (APIs), impurities, and finished products. It is one of the most critical analytical techniques in pharmaceutical quality testing.
2. What are OOS and OOT investigations?
OOS (Out of Specification) refers to test results that fall outside approved specifications, while OOT (Out of Trend) indicates results that deviate significantly from historical trends. Both require systematic investigation to determine root causes and corrective actions.
3. What is ALCOA+ in data integrity?
ALCOA+ stands for Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available. It is a globally accepted framework for ensuring pharmaceutical data integrity and regulatory compliance.
4. What is the purpose of an ETP and MEE system in pharmaceutical manufacturing?
An Effluent Treatment Plant (ETP) treats industrial wastewater before discharge, while a Multiple Effect Evaporator (MEE) concentrates and reduces liquid waste volume. Both systems help organizations meet environmental regulations and sustainability goals.
5. Why is method validation important in Quality Control laboratories?
Method validation demonstrates that an analytical method consistently produces reliable, accurate, and reproducible results. Regulatory agencies require validation to ensure the quality, safety, and efficacy of pharmaceutical products.
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