Looking for QC jobs in Vadodara? Avenza Pharmaceuticals Pvt Ltd is hiring experienced professionals for multiple positions in the Quality Control department. This is an excellent opportunity for candidates with HPLC, method validation, and regulatory exposure for pharma jobs in Gujarat. Build your pharmaceutical career in India with a growing OSD manufacturer.
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About the Company
Avenza Pharmaceuticals Pvt Ltd is a fast-growing pharmaceutical manufacturing company based in Vadodara, Gujarat. Established in 2015, the company specializes in Oral Solid Dosage (OSD) forms including Tablets (General & Effervescent), Capsules, and Suppositories. With a state-of-the-art manufacturing facility spanning over 100,000 sq ft, Avenza focuses on quality, innovation, and regulatory compliance for regulated markets such as USFDA, MHRA, TGA, and EU-GMP.
The company combines production, R&D, and sales under one roof, delivering high-quality healthcare solutions globally. Avenza emphasizes advanced analytical systems and a commitment to building the future of healthcare through excellence and compliance.
Job Details
- Company Name: Avenza Pharmaceuticals Pvt Ltd
- Experience: Varies by role (3–10 years)
- Qualification: B.Pharm / M.Pharm / MSc (relevant experience required)
- Location: Jarod, Samlaya, Vadodara, Gujarat
- Work Type: On-site
Job Description
Avenza Pharmaceuticals is expanding its Quality Control team at the Vadodara manufacturing facility. They are looking for dynamic professionals with strong experience in regulated markets for various QC functions including Stability, Analytical Method Validation (AMV), Process Validation, and Quality Management System (QMS). These roles are critical for maintaining high product quality standards.
Stability Analyst
- Department: Quality Control (Stability)
- Role: Analyst
- Experience: 3 to 5 years
- Education/Qualification: B.Pharm / M.Pharm / MSc
AMV Analyst
- Department: Quality Control (AMV)
- Role: Analyst
- Experience: 5 to 7 years
- Education/Qualification: B.Pharm / M.Pharm / MSc
Process Validation / FP / In-Process Analyst
- Department: Quality Control
- Role: Analyst
- Experience: 3 to 5 years
- Education/Qualification: B.Pharm / M.Pharm / MSc
Process Validation / FP / AMV / Stability Reviewer
- Department: Quality Control
- Role: Reviewer
- Experience: 8 to 10 years
- Education/Qualification: B.Pharm / M.Pharm / MSc
Documentation / QMS (Microbiology)
- Department: Quality Control (Microbiology)
- Role: Documentation / Reviewer / QMS
- Experience: 3 to 5 years
- Education/Qualification: B.Pharm / M.Pharm / MSc
Skills/Qualifications
- Strong experience in HPLC, UV, IR, and chemical testing
- Knowledge of stability sample testing and management
- Hands-on method validation experience
- Expertise in audit trail review and instrument handling (HPLC/UV/IR/GC)
- Proficiency in SOP, STP, SPEC, TDS revision and validation protocols
- Understanding of QMS documentation and reports
- Exposure to regulated markets (USFDA, MHRA, TGA, EU-GMP)
- Good communication and teamwork skills
Key Responsibilities
- Conduct stability sample testing and summary preparation
- Perform HPLC, UV, IR and chemical testing
- Execute analytical method validation
- Support process validation and in-process testing
- Review documents, audit trails, and validation reports
- Revise SOPs, STPs, and validation protocols
- Manage QMS-related documentation and reports
Benefits/Perks
- Career growth in a rapidly expanding company
- Learning opportunities in regulated market operations
- Competitive salary based on experience
- Collaborative and innovative work culture
- Global exposure to international pharmaceutical standards
How to Apply
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Avenza Pharmaceuticals career page.
Interested candidates should send their updated resume to recruitment@avenzapharma.com with the subject line “Application for QC”.
In the mail body, mention:
- Total Experience
- Current CTC
- Expected CTC
- Notice Period
Apply now and take the next step in your pharma career. For more QC jobs and pharmaceutical opportunities across India, visit Pharma Recruiter.
Why You Should Join
Avenza Pharmaceuticals offers a dynamic work environment where your contributions are recognized and valued. Join a company focused on long-term career stability, continuous learning, and professional growth. You will work in a compliance-driven yet innovative setting that supports excellence in pharmaceutical manufacturing and helps you build a rewarding career in the industry.
FAQs
Q1: What qualifications are needed for Avenza QC jobs?
A: Candidates should have B.Pharm, M.Pharm, or MSc with relevant QC experience in OSD formulations.
Q2: How do I apply for these positions?
A: Email your resume to recruitment@avenzapharma.com with the required details in the mail body.
Q3: Is this a walk-in interview?
A: No, applications are accepted via email only. Shortlisted candidates will be contacted.
Q4: What is the experience range for these QC roles?
A: Experience varies from 3–10 years depending on the specific position (Analyst or Reviewer).
