Lupin Limited Hiring for Production, QC, QA

Are you a skilled professional in the pharmaceutical industry looking for rewarding career opportunities? Lupin Manufacturing Solutions Ltd., a leader in API and bulk drug manufacturing, is hiring for multiple roles in Vadodara, Gujarat. With a commitment to innovation, quality, and process safety, Lupin offers a dynamic work environment for professionals in production, quality control, and quality assurance. Explore these exciting pharma job openings and take the next step in your career today!

Available Positions and Responsibilities

1. Production – Jr. Officer/Officer

Join Lupin’s production team to contribute to high-quality API manufacturing in a USFDA/EDQM/TGA-inspected facility.

• Operate and manage API production equipment with precision.
• Ensure compliance with cGMP standards and unit operations/processes.
• Handle plant-specific tasks in shifts, ensuring process safety.
• Maintain documentation and uphold basic GMP and safety protocols.

2. Production (GMP Coordinator) – Officer/Executive

Play a pivotal role in ensuring GMP compliance and quality management.

• Coordinate GMP activities, including change control, CAPA, and deviation initiation.
• Prepare BPR/BCR documentation with accuracy.
• Leverage QAMS expertise to maintain compliance standards.
• Collaborate with cross-functional teams to support production processes.

3. Quality Control – Jr. Officer/Officer

Ensure product quality in Lupin’s API plant with hands-on QC expertise.

• Operate analytical instruments like HPLC, GC, UV, IR, KF, and Auto Titrator.
• Conduct wet lab testing and maintain QAMS documentation.
• Support investigations and comply with ICH/USP guidelines.
• Work on the QC shop floor for USFDA/EDQM/TGA-inspected facilities.

4. QA Analytical Reviewer – Executive

Drive quality assurance through analytical expertise and method validation.

• Review audit trails for software and analytical data.
• Handle advanced instruments like LCMS, GCMS, ICPMS, XRD, TGA, HPLC, GC, FTIR, and UV.
• Perform analytical method validation and transfer activities.
• Ensure compliance with regulatory standards and life cycle management.

Qualifications

• Education: B.Sc., M.Sc., Diploma (Chemical), B.Pharma, or M.Pharma from a recognized institution.
• Experience:
  • Jr. Officer/Officer (Production/QC): 1–6 years in the pharma industry.
  • GMP Coordinator (Officer/Executive): 3–8 years in GMP roles.
  • QA Analytical Reviewer (Executive): 4–8 years in analytical QA.
• Marks Requirement: Minimum 60% or 1st class in highest qualification, unless candidate has 5+ years of documented experience.
• Skills:
  • Production: Knowledge of unit operations, cGMP, and API equipment handling.
  • GMP Coordinator: QAMS expertise, BPR/BCR preparation, change control.
  • Quality Control: HPLC/GC operation, wet lab experience, ICH/USP knowledge.
  • QA Analytical Reviewer: LCMS/GCMS, method validation, audit trail review.

Benefits of Working at Lupin

• Competitive Salary: INR 3,00,000–8,00,000 per annum, based on experience and role.
• Career Growth: Opportunities to work in a globally recognized API facility with USFDA/EDQM/TGA inspections.
• Work Environment: Collaborative, innovative, and safety-focused culture.
• Professional Development: Access to training in cGMP, QAMS, and advanced analytical techniques.
• Location: Vadodara, a hub for pharmaceutical excellence in Gujarat.

How to Apply

Interested candidates should attend the walk-in interview:

• Date: August 13, 2025
• Time: 10:00 A.M. to 4:00 P.M.
• Venue: Lupin Manufacturing Solutions Ltd., Block No. 21, Vill.-Dabhasa, Tal.-Padra, Dist.-Vadodara.
• Requirements: Bring your updated resume, educational certificates, experience letters, and ID proof. Freshers are not eligible.
• Note: Only candidates meeting the 60% marks requirement or with 5+ years of experience should apply.

For more details, visit Pharmabharat.com or contact Lupin’s HR team.

FAQs

1. What documents are required for the walk-in interview?

Bring your updated resume, educational certificates, experience letters, and a valid ID proof. Ensure all documents reflect your qualifications and experience in the pharma industry.

2. Are freshers eligible for these roles?

No, freshers are not eligible. Candidates must have 1–8 years of relevant experience in the pharmaceutical industry, depending on the role.