About the Company
APDM Pharmaceuticals Pvt. Ltd. is a fast-growing Contract Development and Manufacturing Organization (CDMO) founded in June 2022. Based in Ahmedabad, Gujarat, the company specializes in solid oral dosage forms, providing end-to-end formulation development, commercial and clinical supply, and cGMP-compliant manufacturing services.
With a state-of-the-art 15,000-square-meter facility near Ahmedabad equipped with advanced technologies like Wurster coaters, extruders, spheronizers, and IoT-driven systems, APDM serves global markets including the USA, UK, EMEA, Canada, Australia, and PICS countries.
The organization focuses on innovation, quality excellence, ethical partnerships, and scalable solutions to support pharmaceutical partners worldwide. Learn more at the official website: apdmpharma.com.
Job Details
- Company Name: APDM Pharmaceuticals Pvt. Ltd.
- Experience: 0 to 7 Years (varies by role)
- Qualification: M.Sc. / M.Pharm / B.Pharm
- Location: Plant, Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220 (On-site)
- Work Type: On-site
Job Description
APDM Pharmaceuticals is actively hiring skilled talent for its Quality Control and Quality Assurance departments through this walk-in interview. These roles demand hands-on experience with international regulatory audits and a dedication to maintaining high compliance standards in a dynamic CDMO setting.
Trainee / Sr. Officer / Executive / Sr. Executive – Quality Control
- Department: Quality Control
- Experience: 0 to 6 Years
- Education/Qualification: M.Sc. / M.Pharm / B.Pharm
Officer / Sr. Officer / Executive – Quality Assurance
- Department: Quality Assurance
- Experience: 2 to 7 Years
- Education/Qualification: M.Sc. / M.Pharm / B.Pharm
Skills/Qualifications
- Mandatory exposure to EU, MHRA, USFDA, and ANVISA audits / regulatory inspections.
- Solid knowledge of cGMP, GLP, ALCOA++ principles, and GDP.
- Practical expertise in analytical instruments: HPLC, GC, IR, KF, UV, Polarimeter, Dissolution.
- Proven track record in document preparation, review, and compliance adherence.
- Proficiency in analytical method transfer (AMT), method validation (AMV), and API verification.
- Skills in Quality Risk Management (QRM), vendor qualification, technology transfer, and QMS activities.
- Strong planning, coordination, and detail-oriented approach.
Key Responsibilities
- Carry out raw material (RM) sampling and chemical/instrumental analysis.
- Perform finished product (FP), in-process (IP), and stability sample testing.
- Plan, execute, and review AMT, AMV, API verification activities.
- Ensure full GLP compliance and accurate documentation.
- Prepare and review Method of Analysis (MOA), protocols, and reports.
- Manage IPQA, Analytical QA, vendor qualification, and QRM processes.
- Oversee technology transfer and validation (process, cleaning, hold time).
- Handle qualification of equipment, instruments, utilities, and CSV.
- Conduct quality risk assessments and maintain supporting documentation.
Benefits/Perks
- Clear career advancement in a rapidly expanding CDMO.
- Valuable exposure to global regulatory audits and standards.
- Ongoing training in cutting-edge pharmaceutical technologies.
- Supportive, innovation-oriented work culture.
- Long-term stability in Gujarat’s booming pharma sector.
How to Apply
Attend the walk-in interview directly with your updated resume and one passport-size photograph. No pre-registration is needed—simply arrive during the designated hours.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the APDM Pharma LinkedIn page.
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Walk-in Interview Details
- Date: February 24
- Time: 08:30 AM to 03:30 PM
- Venue: Plot No. 775, 776 & 628, Village: Sakodara, Taluka: Bavla, Ahmedabad, Gujarat – 382220
- Instructions: Bring resume and passport-size photo; participate within the time slot.
Why You Should Join
APDM Pharmaceuticals offers a stimulating environment blending regulatory rigor with innovative manufacturing in a modern facility. As a young, ambitious CDMO, it provides direct engagement in global projects and audits from USFDA, MHRA, EU, and ANVISA, helping build deep expertise.
Team members gain continuous professional development, collaborative culture, and defined growth paths. Contribute to a company dedicated to ethical excellence, global reach, and improving health outcomes through top-quality pharmaceutical solutions in India’s vibrant industry hub.
