Aadish Consultancy is organizing a walk-in recruitment drive for Lupin Ltd, Tarapur, a USFDA-approved API manufacturing facility. This opportunity targets freshers and experienced candidates in Production, Quality Control (QC), and Quality Assurance (QA) departments. Candidates with a science background are encouraged to apply.
This drive is scheduled for Sunday, 8th February 2026, at Dombivli East, providing a chance to start or grow your career in the pharmaceutical industry.
Available Positions & Departments
1. Production (API)
- Designation: Sr. Officer / Officer / Associate
- Eligibility: B.Sc./M.Sc./Diploma in Chemical (Male only)
- Experience: Freshers to 5 years
2. Quality Control (QC)
- Designation: Sr. Officer / Officer / Associate
- Eligibility: B.Sc./M.Sc. Chemistry (Male/Female)
- Experience: 0 to 5 years (Analytical Chemistry preferred)
- Skills: HPLC mandatory, GC, KF, GLP/GDP, lab safety, QAMS & LIMS
3. Quality Assurance (QA)
- Designation: Sr. Officer / Officer / Associate
- Eligibility: B.Sc./M.Sc./B.Pharm (Male/Female)
- Experience: 2 to 5 years
- Skills: IPQA, Sampling, Documentation, BPR review, QAMS software
Key Responsibilities
Production:
- Ensure adherence to SOPs, GMP, and safety protocols
- Achieve production targets and manage process-related issues
- Handle centrifuge, reactors, and other manufacturing equipment
Quality Control:
- Perform analytical testing using HPLC, GC, and KF
- Maintain lab safety, follow GLP/GDP standards
- Manage documentation and LIMS/QAMS software
Quality Assurance:
- Conduct IPQA and sampling activities
- Review Batch Production Records (BPR)
- Maintain quality documentation and compliance with SOPs
Qualifications & Experience
- B.Sc./M.Sc./Diploma in Chemical / B.Pharm (depending on department)
- 0-5 years of relevant experience
- Analytical Chemistry knowledge preferred for QC roles
- Freshers eligible for Production & QC roles
Benefits
- Exposure to USFDA-approved API manufacturing
- Hands-on experience in production, QC & QA
- Opportunity to work with advanced instruments and quality systems
- Career growth in a reputed pharmaceutical company
How to Apply / Walk-In Details
- Date: Sunday, 8th February 2026
- Location: Aadish Consultancy, 308, Globe Pinnacle, Opp. Pendharkar College, Next to Royal Enfield Showroom, Dombivli East
- Contact:
- Production: 8169151525
- QC: 9867646673
- QA: 9372148553
- Email: jobs@aadishconsultancy.com
MENTION ” PHARMABHARAT” ON RESUME
Note: Freshers and candidates with relevant experience are encouraged to apply. Male candidates only for Production.
WE DONT TAKE MONEY FROM CANDIDATES | LUPIN TEAM IS COMING | AND YOU WILL GET DIRECT OFFER LETTER ON SPOT | LETS MEET SOON
✅ Production (API) – HR & Technical Questions
HR Questions
- Tell me about yourself and your educational background.
- Why do you want to work in pharmaceutical manufacturing?
- Are you comfortable working in shifts and plant environments?
- How do you handle work pressure and tight production targets?
- Where do you see yourself in 3–5 years?
Technical Questions
- Explain GMP and why it is important in API manufacturing.
- What is the function of a reactor and centrifuge?
- What are SOPs and why must they be followed?
- Explain batch manufacturing process.
- What actions would you take if a deviation occurs?
✅ Quality Control (QC) – HR & Technical Questions
HR Questions
- Why did you choose Quality Control as a career?
- What attracts you to Lupin Ltd?
- How do you manage multiple samples and deadlines?
- Are you open to documentation and repetitive work?
Technical Questions
- What is HPLC and its principle?
- Difference between GC and HPLC.
- What is calibration and why is it required?
- Explain GLP and GDP.
- What is system suitability in HPLC?
- What do you understand by OOS and OOT?
✅ Quality Assurance (QA) – HR & Technical Questions
HR Questions
- Why do you prefer QA over QC or Production?
- How do you ensure compliance in daily activities?
- Describe a situation where you handled a documentation error.
- Are you comfortable with audits and inspections?
Technical Questions
- What is IPQA?
- What is a Batch Production Record (BPR)?
- Difference between deviation, CAPA, and change control.
- What is QMS/QAMS?
- What documents are required for GMP compliance?
🎯 Interview Preparation Tips
- Revise GMP, GLP, GDP, and SOP concepts.
- Be clear about your final-year project or internship.
- Carry updated resume, certificates, and passport-size photos.
- Answer confidently and honestly.
