APDM Pharmaceuticals Walk-in for QC, QA, Engineering & Production Roles in Ahmedabad – October 11-14, 2025

Seize pharma jobs at APDM! Attend walk-in interviews for QC jobs, QA roles, production jobs, and engineering in pharmaceutical careers in India. Regulatory exposure required—apply now in Ahmedabad.

About the Company

APDM Pharmaceuticals Pvt. Ltd., founded in June 2022 in Ahmedabad, Gujarat, is a dynamic contract development and manufacturing organization (CDMO) specializing in solid oral formulations.

Driven by visionary entrepreneurs and seasoned scientists, the company emphasizes innovation, regulatory compliance with EU, MHRA, USFDA, and ANVISA standards, and sustainable growth in the global pharma sector.

As a closely held entity, APDM fosters credibility through advanced R&D and client-focused solutions, exporting quality generics while building a robust presence in regulated markets.

Job Details

• Company Name: APDM Pharmaceuticals
• Experience: 2 to 12 Years (varies by role)
• Qualification: M.Sc./M.Pharm/B.Pharm, ITI/Diploma/BE, 12th Pass
• Location: Sakodara Village, Ahmedabad, Gujarat
• Work Type: On-site

Job Description

APDM Pharmaceuticals is conducting a multi-day walk-in drive to recruit for its expanding operations in quality, production, and engineering. These pharma jobs demand regulatory exposure to EU, MHRA, USFDA, and ANVISA audits. Join a innovative CDMO advancing pharmaceutical careers in India through solid oral expertise.

Quality Control Officer / Sr. Officer

• Department: Quality Control
• Role: Packing Material & Chemical Analysis
• Experience: 2 to 5 Years
• Education/Qualification: M.Sc./M.Pharm

Quality Control Executive / Sr. Executive

• Department: Quality Control
• Role: RM Sampling & Instrumental Analysis
• Experience: 4 to 6 Years
• Education/Qualification: M.Sc./M.Pharm

Quality Control Sr. Executive / Assistant Manager

• Department: Quality Control
• Role: AMT Planning & GLP Compliance
• Experience: 6 to 10 Years
• Education/Qualification: M.Sc./M.Pharm

Quality Control Executive / Sr. Executive (AQA)

• Department: Quality Control
• Role: In-Process & QMS Activities
• Experience: 7 to 9 Years
• Education/Qualification: M.Sc./M.Pharm

Quality Assurance Executive / Sr. Executive / Assistant Manager (IPQA)

• Department: Quality Assurance
• Role: BMR Review & Batch Release
• Experience: 6 to 9 Years
• Education/Qualification: M.Sc./B.Pharm/M.Pharm

Quality Assurance Executive / Sr. Executive (Documentation)

• Department: Quality Assurance
• Role: BMR Issuance & Doc Management
• Experience: 6 to 8 Years
• Education/Qualification: M.Sc./B.Pharm/M.Pharm

Quality Assurance Executive / Sr. Executive (Reviewer Qualification)

• Department: Quality Assurance
• Role: Calibration & HVAC Validation
• Experience: 5 to 7 Years
• Education/Qualification: M.Sc./B.Pharm/M.Pharm

Quality Assurance Sr. Executive / Assistant Manager (Reviewer QMS)

• Department: Quality Assurance
• Role: QMS Document Review
• Experience: 7 to 9 Years
• Education/Qualification: M.Sc./B.Pharm/M.Pharm

Quality Assurance Executive / Sr. Executive (Reviewer Validation)

• Department: Quality Assurance
• Role: Product Launch Documentation
• Experience: 6 to 8 Years
• Education/Qualification: M.Sc./B.Pharm/M.Pharm

Instrumentation Technician

• Department: Engineering
• Role: Equipment Breakdown Repairs
• Experience: 3 to 5 Years
• Education/Qualification: ITI/Diploma

Engineering Officer

• Department: Engineering
• Role: HVAC & Water System Maintenance
• Experience: 3 to 5 Years
• Education/Qualification: BE (Any Stream)

Fitter (Process Equipment)

• Department: Engineering
• Role: Utility Equipment Operations
• Experience: 3 to 5 Years
• Education/Qualification: ITI

Operator (HVAC/Utility)

• Department: Engineering
• Role: System Monitoring & Maintenance
• Experience: 4 to 7 Years
• Education/Qualification: ITI

Electrician

• Department: Engineering
• Role: Electrical Systems Troubleshooting
• Experience: 3 to 5 Years
• Education/Qualification: ITI

Operator (RO)

• Department: Engineering
• Role: Water System Operations
• Experience: 3 to 5 Years
• Education/Qualification: ITI

Production Executive / Sr. Executive (Packaging)

• Department: Production
• Role: Packaging Operations Supervision
• Experience: 4 to 7 Years
• Education/Qualification: B.Pharm/M.Pharm

Production Officer / Sr. Officer (Tablet & Capsule)

• Department: Production
• Role: Manufacturing Equipment Operations
• Experience: 2 to 6 Years
• Education/Qualification: B.Pharm/M.Pharm

Production Assistant Manager

• Department: Production
• Role: Tablet & Capsule Supervision
• Experience: 8 to 12 Years
• Education/Qualification: B.Pharm/M.Pharm

Production Operator (Granulation, Coating & Capsule, Compression, Packaging)

• Department: Production
• Role: Machine Operations in Sections
• Experience: 3 to 5 Years
• Education/Qualification: ITI/12th Pass

Skills/Qualifications

• Expertise in HPLC, GC, UV, IR, KF, Polarimeter, Dissolution
• Knowledge of cGMP, GLP, ALCOA++, GDP compliance
• Experience in SOP preparation, MOA, protocols, method transfer
• Regulatory audit exposure (EU, MHRA, USFDA, ANVISA mandatory)
• Proficiency in BMR/BPR review, deviation investigation, OOS/OOT
• Technical skills in HVAC, utilities, electrical, RO systems
• B.Pharm/M.Pharm for QA/QC; ITI/Diploma/BE for engineering/production

Key Responsibilities

• Perform chemical/instrumental analysis daily
• Review and approve QMS documents promptly
• Maintain HVAC/utilities per SOPs
• Execute production batches with cGMP adherence
• Investigate deviations and ensure audit readiness
• Document operations for regulatory compliance

Benefits/Perks

• Strong career progression in CDMO environment
• Continuous training on regulatory standards
• Competitive salary with audit bonuses
• Supportive culture fostering innovation
• Global exposure via international compliance

How to Apply

Attend the walk-in interview with your resume and one passport-size photo. For additional pharma jobs advice, visit Pharma Recruiter. Secure your spot—walk in today for transformative pharmaceutical careers in India!

Verified Post

The post is released by the APDM Pharmaceuticals LinkedIn page. Click here to visit the post

Walk-in Interview Details

• Date: October 11 to 14, 2025
• Time: 09:30 AM to 04:30 PM
• Venue (QC/QA): 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad
• Venue (Engineering/Production): Plot No. 775, 776 & 628, Vill. Sakodara, Taluka Bavla, Ahmedabad, Gujarat-382220
• What to Bring: Resume and one passport-size photo

Why You Should Join

APDM Pharmaceuticals nurtures a culture of collaboration and excellence, recognized for its rapid growth since 2022 in solid orals CDMO. Enjoy long-term stability through regulatory mastery and R&D innovation, with ample learning opportunities in a compliance-centric setting that propels your QA, QC, and production expertise forward.

FAQs