Pharm'Up 
APDM Pharmaceuticals Private Limited, a global pharmaceutical service provider with extensive experience in CDMO, R&D, and regulatory affairs, is conducting a Walk-In Interview drive for its Quality Control (QC) and Analytical Development (AD) teams in Ahmedabad.
A key requirement for all QC roles is mandatory regulatory exposure to major audits, including EU, MHRA, USFDA, and ANVISA.
Walk-In Interview Details
APDM is conducting interviews at two separate locations based on the department:
- QC Department: Plant location is at Sakodara Village, Ahmedabad.
- Analytical Development (R&D) Department: R&D Unit is at Changodar, Ahmedabad.
| Department | Date | Time | Venue |
| Both QC & Analytical Development | Saturday, 15th November 2025 | 09:30 am to 04:30 pm | 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad |
| Analytical Development Only | Saturday, 15th November 2025 | 09:00 am to 04:30 pm | Unit No. 90 & 91, Parishram Industrial Hub, Chacharwadi – Vasna, Changodar, Ahmedabad |
Please Bring: Your updated Resume and one passport size photograph.
Detailed Job Roles and Requirements
1. Quality Control (QC)
- Location: Plant (Sakodara Vill., Ahmedabad)
- Qualification: M.Sc. / M.Pharm
| Post | Total Vacancies | Experience (Yrs) | Key Skills / Profile Focus |
| Officer / Sr. Officer | 4 | 2 to 5 | Packing material handling and release, UV, IR, KF, Polarimeter, Titration, Chemical Analysis. Preparation of SOP, Specifications (RM/PM/IP/FP/Stability), MOA, Protocols, GTP, Method Transfer/Verification, API Verification, and Documentation. |
| Executive / Sr. Executive | 5 | 4 to 6 | RM Sampling & Analysis (Chemical & Instrumentation). Hands-on experience with HPLC, GC, IR, KF, UV, Polarimeter, Dissolution Chemical Testing, and FP/IP/Stability Analysis (Chemical & Instrumentation). |
| Sr. Exe. / AM / Manager / Dy. Manager | 2 | 6 to 12 | Planning and Review of AMT, AMV, API verification. Overall GLP maintaining & compliance. Preparation of MOA and protocols. Coordination for TT & AMV. Must have strong knowledge of cGMP, GLP, ALCOA++ principle & GDP. |
2. Analytical Development (AD)
- Location: R&D Unit, Changodar
- Qualification: M.Sc. / M.Pharm
- Post: Officer / Sr. Officer / Executive / Sr. Executive (Total 6)
- Experience: 0 to 8 Years
- Key Skills / Profile Focus:
- Analytical Method Development for Assay, Dissolution, Related substance, and other tests for Drug Products.
- Perform Analytical Method Validation, Verification, and Transfer.
- Perform Multimedia Dissolution profiles, R&D stability analysis, and plant support for investigation study.
- Preparation of STP and Specification for Drug Product, Drug substance, and excipient.
- Preparation of Protocol and Report for Analytical Method Validation/Verification/Transfer.
- Maintaining raw data as per GDP/GLP.
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