Join pharma jobs in Vadodara with walk-in interviews at Avenza Pharmaceuticals Pvt Ltd. Experienced professionals needed for OSD formulations roles in Production, Quality Assurance, Quality Control, and AR&D.
About the Company
Avenza Pharmaceuticals Pvt Ltd operates a modern manufacturing facility in Vadodara, Gujarat. The company specializes in Oral Solid Dosage forms, including general and effervescent tablets, capsules, and suppositories.
It holds WHO-GMP and ISO 9001:2008 certifications, ensuring high-quality standards and regulatory compliance. Avenza integrates production, research & development, and sales in a comprehensive unit.
With state-of-the-art manufacturing and ultra-advanced analytical labs, it focuses on innovation and affordable healthcare.
Job Details
- Company Name: Avenza Pharmaceuticals Private Limited
- Experience: 2–8 years (varies by role)
- Qualification: B.Pharm/M.Pharm, B.Sc./M.Sc., ITI/Diploma (varies by role)
- Location: Vadodara, Gujarat
- Work Type: On-site
Job Description
Avenza Pharmaceuticals expands its OSD formulations business in Vadodara. Hiring experienced professionals for Production, Quality Assurance, Quality Control, and Analytical Research & Development.
Immediate joiners preferred in this walk-in interview drive.
Production Department
Officer (AP-PRD-OFF-01)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–8 years
Sr. Officer (AP-PRD-S.OFF-02)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–8 years
Executive (AP-PRD-EXE-03)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–8 years
Operators (AP-PRD-OPR-01)
- Qualification: ITI/Diploma
- Experience: 2–5 years
- Roles: Granulation, Compression, Coating, Capsule Filling, Effervescent Manufacturing, Suppository Manufacturing, Packing (Primary & Secondary), QMS
Quality Assurance Department
Sr. Officer (AP-QA-S.OFF-01)
- Qualification: B.Pharm/M.Pharm
- Experience: 3–7 years
- Roles: Quality Management System, Vendor Management, Stability Management
Executive (AP-QA-EXE-02)
- Qualification: B.Pharm/M.Pharm
- Experience: 3–7 years
- Roles: Quality Management System, Vendor Management, Stability Management
Quality Control Department
Officer (AP-QC-OFF-01)
- Qualification: B.Sc./M.Sc.
- Experience: 2 years minimum
- Roles: Document Management System, Good Laboratory Practices
Sr. Officer (AP-QC-S.OFF-02)
- Qualification: B.Pharm/M.Pharm
- Experience: Up to 8 years
- Roles: Analytical Method Validation, RM/PM Analyst, HPLC/GC Analyst
Executive (AP-QC-EXE-03)
- Qualification: B.Pharm/M.Pharm
- Experience: Up to 8 years
- Roles: HPLC/GC Analyst, Quality Management System, QC Investigation
Analytical Research & Development (AR&D)
Officer (AP-AR&D-OFF-01)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–5 years
- Roles: Method Development, Dissolution Development, Assay, RS Development
Sr. Officer (AP-AR&D-S.OFF-02)
- Qualification: B.Pharm/M.Pharm
- Experience: 2–5 years
- Roles: Method Development, Dissolution Development, Assay, RS Development
Skills/Qualifications
- Experience in OSD manufacturing processes
- Proficiency in granulation, compression, coating, capsule filling
- Knowledge of effervescent and suppository production
- Expertise in HPLC/GC and analytical method development
- Familiarity with QMS, vendor management, stability studies
- Strong understanding of GMP and regulatory guidelines
- Excellent documentation and problem-solving skills
Key Responsibilities
- Execute production processes efficiently
- Operate granulation and compression equipment
- Perform coating and capsule filling operations
- Manufacture effervescent tablets and suppositories
- Handle primary and secondary packing
- Maintain quality management systems
- Conduct analytical testing and validation
- Investigate quality deviations
Benefits/Perks
- Work in WHO-GMP certified facility
- Exposure to advanced manufacturing technology
- Opportunities for professional growth
- Collaborative team environment
- Focus on innovation and quality
- Training in regulatory compliance
- Stable career in expanding company
- Contribution to affordable healthcare
How to Apply
Attend the walk-in with updated resume, latest increment letter, and last 3 months’ salary slips. Email resume with job code in subject to recruitment@avenzapharma.com.
Source
You can view the Source of this post on the Avenza Pharmaceuticals LinkedIn page.
SWalk-in Interview Details
- Dates: 24th, 25th, and 26th December 2025
- Time: 10:00 AM to 04:30 PM
- Venue: Block/Survey No.: 111/1, Jarod-Samalaya Road, Village: Vadadala, Tal. Savli, Dist. Vadodara – 391520
- Note: Do not attend if interviewed in last 6 months or offered a position.
Why You Should Join
Avenza Pharmaceuticals offers a progressive environment with integrated R&D and production. Employees benefit from state-of-the-art facilities and commitment to global standards.
The company emphasizes quality, innovation, and employee development. Join a growing organization dedicated to accessible healthcare solutions. Secure long-term growth in Gujarat’s pharmaceutical hub.
FAQs
What experience levels are required?
Roles need 2–8 years experience depending on position; immediate joiners advantageous.
Can I apply without attending walk-in?
Who cannot attend the interview?
Candidates who participated in interview last 6 months or received an offer.
What career growth is available?
Opportunities in advanced formulations, quality systems, and R&D with progression in a certified facility.