APDM Pharmaceuticals is conducting a walk-in interview on 14 March 2026 for multiple positions in the Quality Control and Quality Control Microbiology departments. The recruitment drive will be held at the company’s manufacturing plant in Sakodara, Bavla (Ahmedabad, Gujarat).

This walk-in opportunity is ideal for B.Pharm, M.Pharm, B.Sc, and M.Sc Microbiology graduates looking to build a career in the pharmaceutical industry. Candidates with 0–7 years of experience in quality control, microbiology testing, and regulatory compliance are encouraged to attend.

The company is seeking professionals with exposure to EU, MHRA, USFDA, and ANVISA regulatory audits, along with strong knowledge of cGMP, GLP, ALCOA++ principles, and Good Documentation Practices (GDP).

Walk-In Interview Details

• Company: APDM Pharmaceuticals
• Interview Date: 14 March 2026
• Reporting Time: 08:30 AM – 03:30 PM
• Job Location: Sakodara Plant, Bavla, Ahmedabad, Gujarat
• Venue: Plot No. 775, 776 & 628, Village Sakodara, Taluka Bavla, Ahmedabad – 382220
• Documents Required: Updated Resume + One Passport Size Photograph

Available Positions

1. Sr. Officer / Executive / Sr. Executive – Quality Control

Department: Quality Control
Experience: 0 – 6 Years
Qualification: M.Sc / M.Pharm / B.Pharm

Key Responsibilities

• Perform raw material sampling and analysis using chemical and instrumentation techniques.
• Handle instruments such as HPLC, GC, IR, KF, UV, Polarimeter, and Dissolution systems.
• Conduct chemical testing, FP/IP analysis, and stability studies.
• Plan and execute AMT and AMV activities.
• Review API verification data and analytical reports.
• Maintain Good Laboratory Practices (GLP) and documentation.
• Prepare method of analysis (MOA), protocols, and analytical reports.
• Coordinate with teams for technology transfer and validation activities.
• Ensure compliance with cGMP, ALCOA++, and GDP requirements.

2. Sr. Officer / Executive / Sr. Executive – QC Microbiology

Department: Quality Control Microbiology
Experience: 2 – 7 Years
Qualification: B.Sc / M.Sc Microbiology

Key Responsibilities

• Conduct microbiological testing of raw materials and finished products.
• Perform microbial limit tests, sterility testing, and microbial identification.
• Execute environmental monitoring in cleanrooms and controlled areas.
• Manage water system monitoring and microbial culture maintenance.
• Prepare and maintain culture media and laboratory reagents.
• Ensure GMP compliance and regulatory documentation integrity.
• Support OOS investigations, deviations, and contamination control activities.
• Maintain laboratory equipment calibration and validation records.

Required Skills

Candidates applying for APDM pharmaceutical jobs should have:

• Experience with USFDA, EU, MHRA, and ANVISA regulatory environments
• Strong knowledge of cGMP, GLP, and data integrity practices
• Experience in documentation review and laboratory compliance
• Analytical skills in pharmaceutical QC testing and microbiology analysis

Qualifications

Eligible candidates must possess one of the following:

• B.Pharm / M.Pharm
• M.Sc (Chemistry or related field)
• B.Sc / M.Sc Microbiology

Experience requirements vary from 0 to 7 years depending on the role.

Benefits of Working at APDM Pharmaceuticals

• Opportunity to work in a regulated pharmaceutical manufacturing environment
• Exposure to global regulatory audits (USFDA, EU, MHRA, ANVISA)
• Hands-on experience with advanced analytical instrumentation
• Professional growth in quality control and microbiology operations