Avenza Pharmaceuticals Walk-in Quality Control
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- Summary Table
QC Openings for Experienced Pharma Candidates in Vadodara
Avenza Pharmaceuticals hiring experienced QC professionals for multiple sections. Walk-in for 2–10 yrs experienced candidates in Vadodara.
Intro Paragraph
Avenza Pharmaceuticals is hiring experienced Quality Control professionals for its advanced OSD formulation facility. The company is conducting a multi-day walk-in drive for candidates who have worked in regulated market environments and can manage QC activities with precision. These openings fit professionals who want a stable career in analytical operations, GLP systems, method validation, and regulated market compliance.
Company Overview
Avenza Pharmaceuticals Pvt. Ltd. is a growing pharmaceutical manufacturer with a strong focus on OSD formulations, including tablets, effervescent tablets, capsules, and suppositories. The company operates with a compliance-driven approach and supports submissions across regulated markets such as USFDA, MHRA, TGA, and EU-GMP. Its Vadodara facility is structured around modern QC labs, validated equipment, and disciplined documentation systems. This setup provides a strong environment for QC professionals aiming to build expertise in high-demand analytical operations.
Job Role & Responsibilities
Openings are available across multiple QC functions. Depending on experience and specialization, responsibilities include:
- Managing GLP activities and ensuring data integrity across QC workflows
- Reviewing analytical reports, raw data, and documentation
- Handling HPLC testing and open lab operations
- Supporting QMS activities, including change control and deviation management
- Conducting QC investigations and documenting findings
- Performing raw material and packaging material testing (RM/PM)
- Supporting analytical method validation activities
- Conducting microbiology testing as per regulatory requirements
Candidates must have experience in regulated market operations and the ability to meet submission-driven timelines.
Eligibility / Qualifications
Required Education:
- B.Sc
- M.Sc
Relevant courses include: Chemistry, Analytical Chemistry, Organic Chemistry, Pharmaceutical Chemistry, Industrial Chemistry, Microbiology, Biochemistry, Biotechnology.
Experience required:
- 2 to 10 years, depending on the QC section
Available QC Sections:
- GLP (4–8 yrs)
- QC Reviewer (8–10 yrs)
- HPLC – Open Lab (4–7 yrs)
- QMS (5–8 yrs)
- QC Investigation (4–6 yrs)
- RM/PM Analyst (2–3 yrs)
- Analytical Method Validation (4–7 yrs)
- QC Micro (2–5 yrs)
Location & Salary
Location: 111/1, Jarod-Samalaya Road, At Vadadala, Tal. Savli, Dist. Vadodara – 391520.
Salary: Based on experience and company standards.
Application Process
Walk-in Interview Dates:
- 22 November 2025 (Saturday)
- 23 November 2025 (Sunday)
- 24 November 2025 (Monday)
Time: 10:00 AM – 04:00 PM
Candidates must bring:
- Updated CV
- Last 3 months’ salary slips
- Current CTC structure
FAQs
What experience is required?
Between 2 to 10 years depending on the QC section.
Which dosage forms does Avenza handle?
Tablets, effervescent tablets, capsules, and suppositories.
Are these roles for regulated markets?
Yes. Experience with USFDA, MHRA, TGA, and EU-GMP operations is preferred.
Do candidates need strong HPLC experience?
Yes. Several openings require functional HPLC hands-on experience.
Is there any online application link?
Walk-in only. Candidates should attend with required documents.
Summary Table
| Category | Details |
|---|---|
| Company | Avenza Pharmaceuticals Pvt. Ltd. |
| Vacancies | QC openings across multiple sections |
| Required Education | B.Sc, M.Sc |
| Experience | 2–10 years |
