Avenza Pharmaceuticals Pvt. Ltd. is hiring experienced pharmaceutical quality professionals for multiple Quality Control (QC) positions at its facility in Jarod, Samlaya, Vadodara, Gujarat. Candidates with 3–5 years of pharmaceutical industry experience and knowledge of cGMP, regulatory requirements, SOPs and quality documentation can apply.
Company: Avenza Pharmaceuticals Pvt. Ltd.
Department: Quality Control (QC)
Experience: 3–5 Years
Location: Jarod, Samlaya, Vadodara, Gujarat
Job Type: Full-time
Openings: 5 positions
Author: Pharmabharat Editorial Team
Avenza Pharmaceuticals QC Jobs 2026
Avenza Pharmaceuticals Pvt. Ltd. is expanding its Quality Control team and has announced openings across several QC functions. The company is seeking professionals who can contribute to pharmaceutical quality, compliance, documentation and laboratory operations.
The current recruitment drive includes openings for QC Reviewer – HPLC/GC, QC QMS and QC Documentation. Candidates should have relevant pharmaceutical industry experience and a strong understanding of applicable regulations, standard operating procedures and current Good Manufacturing Practices (cGMP).
The company states that its plant is HPRA Approved and WHO Approved.
Available QC Positions
| Position | Experience | Vacancies |
|---|---|---|
| QC Reviewer – HPLC/GC | 3–5 Years | 2 |
| QC QMS | 3–5 Years | 1 |
| QC Documentation | 3–5 Years | 1 |
| Additional QC Position | 3–5 Years | 1 |
Total reported openings: 5
QC Reviewer – HPLC/GC
The QC Reviewer – HPLC/GC position is suitable for professionals experienced in pharmaceutical quality control and analytical laboratory activities.
Candidates should be familiar with HPLC/GC-related documentation, review processes, laboratory compliance and pharmaceutical quality requirements.
Key areas may include:
- Review of analytical and QC documentation
- HPLC/GC-related quality control records
- Compliance with approved SOPs
- Review of laboratory records and supporting documents
- Ensuring adherence to cGMP requirements
- Supporting investigation and documentation activities where applicable
QC QMS
The QC QMS position focuses on quality management activities within the Quality Control function.
Professionals applying for this position should understand pharmaceutical quality systems, documentation practices, SOP compliance and applicable regulatory requirements.
QC Documentation
The QC Documentation position is focused on maintaining accurate and compliant quality documentation.
Strong documentation skills, attention to detail and familiarity with pharmaceutical quality systems are important for this role.
Key Requirements
Candidates applying for these Avenza Pharmaceuticals QC jobs should meet the following requirements:
- 3–5 years of relevant pharmaceutical industry experience
- Knowledge of applicable pharmaceutical regulations
- Understanding of cGMP requirements
- Familiarity with SOPs and quality systems
- Strong documentation skills
- Good communication skills
- Ability to work effectively in a team
- Ability to meet deadlines and manage assigned responsibilities
- Relevant experience in Quality Control or related pharmaceutical quality functions
Experience related to HPLC, GC, QC review, QMS or pharmaceutical documentation will be particularly relevant depending on the position.
Educational Qualification
The supplied recruitment announcement does not specify a particular educational qualification.
Candidates should therefore refer to their relevant academic and professional qualifications in their updated resume and confirm role-specific eligibility with the recruiter.
Salary / CTC
Salary: Not disclosed by Avenza Pharmaceuticals in the recruitment announcement.
For reference only, the indicative market range for experienced pharmaceutical QC professionals with 3–5 years of experience in the Vadodara/Gujarat market may be approximately ₹4.5–7.5 LPA, depending on role, analytical expertise, employer, qualifications and experience.
Important: This is a market estimate and is not an employer-confirmed salary range.
Why Consider These Avenza Pharmaceuticals QC Opportunities?
These positions may be relevant for pharmaceutical professionals looking to develop their careers in:
- Pharmaceutical Quality Control
- HPLC/GC operations and review
- Quality Management Systems
- QC documentation
- cGMP compliance
- Pharmaceutical regulatory compliance
- Quality assurance and laboratory processes
Avenza Pharmaceuticals describes itself as a growing pharmaceutical company focused on quality, compliance and better healthcare.
Work Location
The positions are based at:
Avenza Pharmaceuticals Pvt. Ltd.
Jarod, Samlaya, Vadodara, Gujarat, India
The recruitment announcement identifies the facility as an HPRA Approved Plant and WHO Approved Plant.
How to Apply for Avenza Pharmaceuticals Jobs
Interested and eligible candidates should send their updated resume to:
