APDM Pharmaceuticals, a growing name in the Indian pharmaceutical sector focused on creating a healthy future, is actively recruiting talented professionals for its plant in Sakodara, Gujarat. The company has announced a walk-in interview drive for key positions in Quality Control (QC) and Quality Assurance (QA) departments.
This is an excellent opportunity for candidates with experience in analytical techniques, regulatory audits (EU, MHRA, USFDA, ANVISA), and compliance standards like cGMP, GLP, and GDP. The walk-in is scheduled for February 24, 2026, from 08:30 AM to 03:30 PM at the plant location.
Available Positions and Departments
- Trainee / Sr. Officer / Executive / Sr. Executive – Quality Control Experience: 0 to 6 years Qualification: M.Sc./M.Pharm / B.Pharm
- Officer / Sr. Officer / Executive – Quality Assurance Experience: 2 to 7 years Qualification: M.Sc./M.Pharm / B.Pharm
Candidates with exposure to EU, MHRA, USFDA, and ANVISA audits/regulatory inspections are strongly preferred.
Key Skills and Responsibilities
For Quality Control Roles:
- Raw Material (RM) sampling and analysis using instruments like HPLC, GC, IR, KF, UV, Polarimeter
- Chemical and instrumentation testing for Finished Product (FP), In-Process (IP), and Stability samples
- Dissolution testing and related chemical analysis
- Planning and execution of Analytical Method Transfer (AMT), Analytical Method Validation (AMV), and API verification
- Review of documents, maintaining GLP compliance
- Preparation of Method of Analysis (MOA) and protocols
- Coordination for Technology Transfer (TT) and AMV
- Overall adherence to cGMP, GLP, ALCOA++ principles, and Good Documentation Practices (GDP)
- Strong experience in document preparation and review is mandatory
For Quality Assurance Roles:
- In-Process QA (IPQA) activities
- Analytical QA oversight
- Vendor qualification and Quality Risk Management (QRM)
- Technology Transfer processes
- Validation activities including Process, Cleaning, Hold Time, Utility, Equipment/Instrument, and Computer System Validation (CSV)
- Quality Risk Assessment
- Documentation and QMS (Quality Management System) handling
These roles demand hands-on experience in regulated environments and a commitment to quality standards in API/pharmaceutical manufacturing.
Salary and Benefits
While exact salary figures are not disclosed in the announcement, typical ranges for these positions in Gujarat pharmaceutical plants are:
- Entry-level/Trainee (0-2 years): ₹2.5 – 4.5 LPA
- Mid-level (2-6 years): ₹4 – 8 LPA
- Senior roles (5+ years): ₹6 – 12 LPA or higher, depending on expertise and regulatory exposure
Benefits often include PF, ESI, health insurance, performance incentives, and transport facilities (common in plant locations like Sakodara). Final offers depend on interview performance and negotiation.
How to Apply
This is a walk-in interview opportunity—no prior application required. Date: February 24, 2026 Time: 08:30 AM to 03:30 PM Venue: APDM Pharmaceuticals Plant, Plot No. 775, 776 & 628, Village: Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220
Instructions:
- Bring your updated resume and one passport-size photograph.
- Candidates are advised to arrive early to avoid waiting.
- Prior experience in regulatory audits and document handling will be a key advantage.
Don’t miss this chance to join APDM Pharmaceuticals and contribute to quality-driven pharmaceutical manufacturing. Prepare your documents and head to the venue on February 24!
