Walk-in Interview at Avenza Pharmaceuticals Hiring for Production, QA, QC & AR&D Jobs (24-26 Dec 2025)

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.

Immediate availability preferred. Advance your career in formulations—apply now! Explore more pharma jobs at Pharma Recruiter.

Walk-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.

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