APDM Pharmaceuticals is hosting a walk-in interview for Quality Control roles in Chemical and Microbiology departments. This is a great opportunity for pharma professionals with regulatory exposure to join a growing CDMO in Gujarat. Explore exciting pharma jobs, QC jobs, and pharmaceutical careers in India today.
Contents
About the Company
APDM Pharmaceuticals Pvt. Ltd. is a dynamic Contract Development and Manufacturing Organization (CDMO) founded in June 2022. Headquartered in Ahmedabad, Gujarat, the company operates a state-of-the-art manufacturing facility spanning 15,000 square meters in Sakodara, Bavla.
Specializing in solid oral dosage forms (with capabilities in injectables, ophthalmics, and semisolids), APDM serves global markets including the USA, UK, EMEA, Canada, Australia, and PICS countries. Committed to innovation, quality, transparency, and regulatory excellence, APDM empowers partners with end-to-end formulation support, commercial & clinical supply, and world-class GMP standards.
Job Details
- Company Name: APDM Pharmaceuticals Pvt. Ltd.
- Experience: 0 to 7 years (varies by role)
- Qualification: M.Sc. / M.Pharm / B.Pharm; B.Sc. / M.Sc. (Microbiology)
- Location: Plant, Sakodara, Taluka Bavla, Ahmedabad, Gujarat – 382220
- Work Type: On-site
Job Description
APDM Pharmaceuticals is actively recruiting skilled professionals for its Quality Control department to ensure product quality, regulatory compliance, and data integrity in a fast-paced GMP environment. These positions are ideal for candidates experienced in analytical and microbiological testing, supporting global regulatory audits.
Sr. Officer / Executive / Sr. Executive – Quality Control (Chemical)
- Department: Quality Control
- Market: EU, MHRA, USFDA & ANVISA
- Role: Sr. Officer / Executive / Sr. Executive
- Experience: 0 to 6 years
- Education/Qualification: M.Sc. / M.Pharm / B.Pharm
Sr. Officer / Executive / Sr. Executive – Quality Control Microbiology
- Department: Quality Control Microbiology
- Market: EU, MHRA, USFDA & ANVISA
- Role: Sr. Officer / Executive / Sr. Executive
- Experience: 2 to 7 years
- Education/Qualification: B.Sc. / M.Sc. (Microbiology)
Skills / Qualifications
- Mandatory exposure to EU, MHRA, USFDA, and ANVISA audits / regulatory requirements
- In-depth knowledge of cGMP, GLP, ALCOA++ principles, and GDP
- Proven experience in document preparation, review, and compliance
- Strong focus on data integrity and laboratory best practices
- For Chemical QC: Hands-on expertise with HPLC, GC, IR, KF, UV, Polarimeter, Dissolution apparatus
- For Microbiology QC: Proficiency in pharmacopeial methods, microbial techniques, and environmental monitoring
Key Responsibilities
Quality Control (Chemical):
- Conduct raw material sampling and analysis using advanced instrumentation
- Perform finished product, in-process, and stability sample testing
- Plan and execute analytical method transfer (AMT) and validation (AMV)
- Verify APIs, review results, and maintain GLP compliance
- Prepare MOAs, protocols, and coordinate technology transfer activities
Quality Control Microbiology:
- Execute microbiological testing of raw materials, finished products, and water systems
- Perform microbial limit tests, sterility testing, and culture identification
- Carry out environmental monitoring in cleanrooms and controlled areas
- Prepare culture media, maintain cultures, and calibrate laboratory equipment
- Investigate OOS results, deviations, and support contamination control programs
Benefits / Perks
- Strong career progression in a rapidly expanding global CDMO
- International regulatory exposure and market knowledge
- Continuous learning in advanced pharmaceutical technologies
- Positive, collaborative, and innovation-focused work culture
- Opportunity to contribute to high-quality healthcare solutions worldwide
How to Apply
Prepare your updated resume and one passport-size photograph. Attend the walk-in interview directly at the venue.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the APDM LinkedIn page.
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Walk-in Interview Details
- Date: March 14
- Time: 08:30 AM to 03:30 PM
- Venue: Plot No. 775, 776 & 628, Village: Sakodara, Taluka: Bavla, Ahmedabad, Gujarat – 382220
Why You Should Join
APDM Pharmaceuticals combines entrepreneurial vision with scientific expertise to deliver exceptional quality and innovation. With rapid growth since 2022, the company offers long-term stability, hands-on experience with stringent global audits, and a supportive environment for professional development.
Join APDM to build a meaningful career while contributing to safer, more effective medicines on a global scale.
FAQs
What experience levels are required for these QC positions?
Experience ranges from 0–6 years for QC Chemical and 2–7 years for QC Microbiology, with mandatory regulatory audit exposure (EU, MHRA, USFDA, ANVISA).
Is audit experience compulsory?
Yes, prior exposure to EU, MHRA, USFDA, and ANVISA audits or regulatory requirements is essential for both roles.
What documents should I bring to the walk-in?
Bring an updated resume and one passport-size photo. Interviews are held from 08:30 AM to 03:30 PM on the specified date.
What growth opportunities exist at APDM Pharmaceuticals?
The company provides excellent scope for career advancement, global exposure, skill enhancement, and professional growth in a dynamic CDMO setting.
