Are you passionate about creating a healthier future? APDM Pharmaceuticals, a leading name in the pharmaceutical industry, is hosting walk-in interviews for multiple roles at their state-of-the-art facility in Sakodara, Ahmedabad. With opportunities in Quality Control, Quality Assurance, Engineering, and Production, this is your chance to join a dynamic team committed to excellence. The interviews are scheduled from October 11 to October 14, 2025, from 9:30 AM to 4:30 PM. Explore rewarding pharmaceutical careers with APDM and take the next step in your professional journey.
Job Responsibilities
Quality Control (M.Sc./M.Pharm)
- Officer/Senior Officer (4 Positions, 2-5 Years Experience): Conduct sampling, testing, and release of packaging materials using UV, IR, KF, Polarimeter, Titration, and Chemical Analysis. Prepare SOPs, specifications, and protocols. Support method transfer, API verification, and regulatory audits (EU, MHRA, USFDA, ANVISA).
- Executive/Senior Executive (5 Positions, 4-6 Years Experience): Perform RM sampling, chemical and instrumentation analysis (HPLC, GC, IR, UV, Dissolution). Conduct FP/IP/Stability testing and ensure compliance with cGMP standards.
- Senior Executive/Assistant Manager (1 Position, 6-10 Years Experience): Plan AMT, AMV, and API verification. Maintain GLP compliance, prepare MOA, and coordinate technology transfer. Ensure adherence to cGMP and ALCOO++ principles.
- Executive/Senior Executive (AQA) (2 Positions, 7-9 Years Experience): Manage in-process AQA, QMS activities, and investigate deviations, OOS, and OOT results.
Quality Assurance (M.Sc./B.Pharm/M.Pharm)
- Executive/Senior Executive/Assistant Manager (IPQA) (6-9 Years Experience): Draft and review BMR/BPR, ensure batch release, and prepare for regulatory audits.
- Executive/Senior Executive (Documentation) (1 Position, 6-8 Years Experience): Manage BMR/BPR issuance, logbooks, and SOP reviews.
- Executive/Senior Executive (Reviewer Qualification) (1 Position, 5-7 Years Experience): Oversee reviewer qualification, layouts, VMP, and HVAC validation.
- Senior Executive/Assistant Manager (Reviewer QMS) (1 Position, 7-9 Years Experience): Approve QMS documents and ensure compliance with cGMP and ISO standards.
- Executive/Senior Executive (Reviewer Validation) (1 Position, 6-8 Years Experience): Coordinate documentation for product launches and regulatory compliance.
Engineering (ITI/Diploma/BE)
- Instrumentation Technician (1 Position, 3-5 Years Experience): Troubleshoot automation-based process and utility equipment.
- Officer (2 Positions, 3-5 Years Experience): Manage HVAC and water system operations, ensuring SOP compliance.
- Fitter (1 Position, 3-5 Years Experience): Maintain utility equipment (AHU, Chiller, Boiler) and ensure cGMP compliance.
- Operator (HVAC/Utility) (1 Position, 4-7 Years Experience): Monitor and maintain HVAC/utility systems and support qualification activities.
- Electrician (1 Position, 3-5 Years Experience): Install and troubleshoot electrical systems, ensuring cGMP compliance.
- Operator (RO) (1 Position, 3-5 Years Experience): Operate and maintain RO and purified water systems, ensuring water quality.
Production (B.Pharm/M.Pharm/ITI/12th Pass)
- Executive/Senior Executive (Packaging) (1 Position, 4-7 Years Experience): Supervise packaging operations and ensure cGMP/GDP compliance.
- Officer/Senior Officer (Tablet & Capsule) (2 Positions, 2-6 Years Experience): Operate tablet/capsule manufacturing equipment and ensure in-process checks.
- Assistant Manager (2 Positions, 8-12 Years Experience): Supervise tablet/capsule production and ensure regulatory compliance.
- Operator (Granulation, Coating, Capsule, Compression, Packaging) (4 Positions, 3-5 Years Experience): Operate production machines and maintain cGMP standards.
Qualifications
- Education: M.Sc., B.Pharm, M.Pharm, ITI, Diploma, BE, or 12th Pass, depending on the role.
- Experience: 2-12 years in pharmaceutical manufacturing, quality control, quality assurance, or engineering.
- Skills: Knowledge of cGMP, GLP, GDP, HPLC, GC, UV, IR, and regulatory audits (EU, MHRA, USFDA, ANVISA). Strong documentation and analytical skills.
- Certifications: Regulatory audit exposure is mandatory for most roles.
Benefits
- Competitive salary packages (₹3,00,000 – ₹8,00,000 per annum, based on experience and role).
- Opportunities for career growth in a leading pharmaceutical company.
- Exposure to global regulatory standards (EU, MHRA, USFDA, ANVISA).
- Supportive work environment with a focus on innovation and teamwork.
How to Apply
Attend the walk-in interviews from October 11 to October 14, 2025, between 9:30 AM and 4:30 PM at the following venues:
- Quality Control/Quality Assurance/Production: 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad.
- Engineering: Plot No. 775, 776 & 628, Vill. Sakodara, Taluka Bavla, Ahmedabad, Gujarat-382220.
Requirements: Bring your updated resume and one passport-size photograph. Ensure you meet the experience and skill requirements for the desired role.
For more details, visit Pharmabharat.com or contact the APDM Pharmaceuticals HR team.
FAQs
1. What documents are required for the walk-in interview?
Bring an updated resume and one passport-size photograph. Additional documents like educational certificates and experience letters may be requested during the interview.
2. Are freshers eligible for these pharmaceutical jobs?
Most roles require 2-12 years of experience. However, candidates with relevant qualifications and minimal experience may be considered for entry-level operator positions.
