Avenza Pharmaceuticals Pvt. Ltd., a fast-growing company in the Pharmaceuticals (OSD Formulation) segment, is inviting applications from young and dynamic professionals with proven track records in regulated market operations. If you are a professional with experience in Tablets (General & Effervescent), Capsules, and Suppositories, this is the right opportunity to build your career with us.
We are looking for skilled individuals who are passionate about quality, compliance, and innovation, with strong exposure to international standards such as USFDA, MHRA, TGA, and EU-GMP.
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Why Join Avenza Pharmaceuticals?
- Opportunity to work in a global regulatory environment
- Exposure to advanced pharmaceutical manufacturing and cGMP practices
- Professional growth in Quality Control and Quality Systems
- Collaborative work culture driven by innovation & compliance
Current Openings in Quality Control (QC)
QC – GLP (Good Laboratory Practice)
- Experience: 4 to 8 years
- Gender: Male only
- Hands-on exposure to GLP compliance, regulated lab environments, and analytical testing.
QC – HPLC (Open Lab)
- Experience: 4 to 7 years
- Gender: Male only
- Strong expertise in HPLC operations within Open Lab environment. Practical knowledge of advanced chromatographic techniques and documentation is essential.
QMS (Quality Management System)
- Experience: 5 to 8 years
- Skilled in documentation, audit handling, SOP management, deviation control, CAPA, and compliance documentation.
QC Investigation
- Experience: 4 to 6 years
- Gender: Male only
- Exposure to root cause analysis (RCA), OOS, OOT investigations, and corrective & preventive action documentation.
RM/PM Analyst (Raw Material / Packaging Material)
- Experience: 2 to 3 years
- Gender: Male only
- Responsible for analytical testing of raw materials and packaging materials in compliance with GLP/GMP standards.
Candidate Profile
We are looking for professionals who:
- Come from a pharma OSD formulation background.
- Have solid exposure to regulated markets (USFDA, MHRA, TGA, EU-GMP).
- Are capable of handling quality documentation and compliance requirements.
- Are team-oriented, detail-focused, and compliance-driven.
Application Process
Interested candidates are invited to apply immediately by sending their updated resume.
- Email ID: seema@avenzapharma.com
- Subject Line Format: Application for QC-GLP/QMS/etc.
Location: Vadodara
Candidates are advised to clearly mention the department they are applying for in the subject line to ensure faster response.
Important Notes
- Only candidates from the pharma industry (OSD Formulation background) will be considered.
- Positions marked with Male only are restricted due to operational requirements.
- Avenza Pharmaceuticals does not engage agents or consultants charging recruitment fees. Applicants should beware of such fraudulent calls.
About Avenza Pharmaceuticals Pvt. Ltd.
Avenza Pharmaceuticals Pvt. Ltd. is committed to delivering high-quality pharmaceutical formulations for both domestic and global markets. With a state-of-the-art manufacturing facility at Vadodara, we ensure compliance with stringent international guidelines and regulatory standards.
Our goal is to touch lives worldwide by ensuring the highest quality medicines, backed by research, innovation, and uncompromising quality standards.
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