APDM Pharmaceuticals Hiring for Quality Control & Quality Assurance Jobs

APDM Pharmaceuticals is conducting a walk-in interview on 20 January 2026 for experienced QC and QA professionals. Regulatory exposure to EU, MHRA, USFDA & ANVISA is mandatory. Excellent opportunity for pharma jobs in Ahmedabad.

About the Company

APDM Pharmaceuticals is a quality-focused pharmaceutical manufacturing company with a strong emphasis on international regulatory compliance. The organization operates in a highly regulated environment, maintaining exposure to stringent standards set by EU, MHRA, USFDA, and ANVISA.

With modern facilities and a commitment to cGMP and data integrity principles, APDM provides a professional platform for talented individuals to grow in the competitive pharmaceutical sector.

Job Details

• Company Name: APDM Pharmaceuticals
• Experience: 4–6 years
• Location: Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220
• Work Type: On-site

Job Description

APDM Pharmaceuticals is hiring experienced professionals for critical roles in Quality Control and Quality Assurance departments. These positions demand hands-on regulatory exposure and technical expertise in high-compliance manufacturing environments.

Executive / Senior Executive – Quality Control

• Department: Quality Control
• Role: Executive / Senior Executive
• Experience: 4–6 years
• Key Requirement: EU, MHRA, USFDA & ANVISA audits/regulatory exposure mandatory

Officer / Senior Officer / Executive – Quality Assurance

• Department: Quality Assurance
• Role: Officer / Senior Officer / Executive
• Experience: 4–6 years
• Key Requirement: EU, MHRA, USFDA & ANVISA audits/regulatory exposure mandatory

Skills/Qualifications

• Mandatory exposure to EU, MHRA, USFDA & ANVISA audits and regulatory requirements
• Proficiency in chemical and instrumentation analysis (HPLC, GC, IR, KF, UV, Polarimeter, Dissolution)
• Experience in RM sampling, FP/IP/Stability testing, AMT/AMV planning, and API verification
• Strong knowledge of cGMP, GLP, ALCOA++ principles, and GDP
• Expertise in documentation preparation and review
• Hands-on experience in IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, and Documentation

Key Responsibilities

• Conduct RM sampling and chemical/instrumentation analysis
• Perform FP, IP, and stability sample testing
• Plan and coordinate AMT, AMV, and technology transfer
• Handle IPQA and vendor qualification activities
• Manage QMS elements including deviations and CAPA
• Ensure validation, qualification, and documentation compliance
• Maintain GLP, cGMP, and data integrity standards

Benefits/Perks

• Opportunity to work in a highly regulated environment
• Exposure to international audits and standards
• Professional growth in quality systems
• Stable employment in a compliance-driven organization
• Platform to enhance technical and regulatory expertise

How to Apply

Candidates are requested to attend the walk-in interview in person. Please carry your updated resume and one passport-size photograph. Take the next step in your pharmaceutical career – attend the walk-in on 20 January 2026!

For the latest pharma jobs and walk-in updates across India, visit Pharma Recruiter.

Walk-in Interview Details

• Date: 20 January 2026
• Time: 8:30 AM to 3:30 PM
• Venue: Plot No. 775, 776 & 628, Village: Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220
• Documents to Carry: Updated Resume & One Passport-Size Photograph

Why You Should Join

APDM Pharmaceuticals offers a challenging yet rewarding environment for quality professionals who thrive under international regulatory standards. Working here means direct involvement in audits from globally recognized agencies, continuous learning in advanced quality systems, and contribution to high-standard pharmaceutical manufacturing.

The company values technical excellence, documentation accuracy, and compliance commitment, making it an ideal workplace for long-term career growth in the pharmaceutical industry.

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