Attend Lupin Ltd walk-in interview at Hotel Red Maple, Indore on 14th September 2025 for Quality Control (API & FML) and Quality Assurance (API & FML) positions. Openings for B.Sc, M.Sc (Chemistry), B.Pharm candidates with 2–5 years’ experience. Apply now for a pharma career at Mandiddep (Bhopal) facility.
Lupin Ltd Walk-In Interview – Indore (Mandiddep Unit) – QC & QA Openings – 14th September 2025
Are you a pharmaceutical professional looking for an excellent opportunity to work with a leading pharma organization? Lupin Ltd, one of India’s top pharmaceutical companies, is conducting a walk-in interview for multiple positions in Quality Control (QC – API & FML) and Quality Assurance (QA – API & FML) for its Mandiddep (Bhopal) facility.
📍 Walk-In Interview Details
- Company: Lupin Ltd
- Location: Mandiddep (Bhopal), Madhya Pradesh
- Venue: Hotel Red Maple, Indore
- Date: 14th September 2025 (Sunday)
- Time: 10:00 AM to 3:00 PM
- Departments Hiring: Quality Control (API & FML), Quality Assurance (API & FML)
- Qualification: B.Sc / M.Sc (Chemistry) / B.Pharm
- Experience: 2–5 Years
💼 Quality Control (API & FML) – Roles and Responsibilities
The Quality Control team plays a vital role in ensuring product quality and regulatory compliance. Selected candidates will be responsible for:
- Sampling and testing of raw materials, excipients, and packing materials.
- Performing analysis using advanced analytical instruments such as HPLC, GC, LCMS, GCMS, IR, UV, Dissolution, Polarimeter, Potentiometric titrations, KF, and PSD analysis using Malvern.
- Conducting wet chemical and physical analysis as per standard operating procedures (SOPs).
- Executing stability studies and preparing related documentation.
- Ensuring compliance with cGMP guidelines and data integrity requirements.
- Handling deviations, OOS (Out of Specification) and OOT (Out of Trend) investigations.
- Maintaining accurate documentation and adherence to regulatory standards.
📋 Quality Assurance (API & FML) – Roles and Responsibilities
QA professionals are expected to review and maintain compliance with regulatory requirements. Responsibilities include:
- Review of Batch Production Records (BPR), batch cleaning records, and test data sheets.
- Preparation of Annual Product Quality Review (APQR).
- Review of Change Control, Deviations, CAPA, OOS, and OOT documentation.
- Responding to customer queries and preparing regulatory questionnaires.
- Reviewing qualification and validation documents, investigation reports, and Quality Risk Management (QRM) data.
- Reviewing analytical documents, method validation reports, specifications, and test methods.
- Conducting audit trail reviews of analytical tests and QC systems to ensure compliance with data integrity standards.
✅ Eligibility Criteria
- Candidates must have secured a minimum of 60% in their highest educational qualification (for candidates with less than 5 years of experience).
- Candidates who have appeared for an interview with Lupin Ltd in the last six months are not eligible.
- Good knowledge of cGMP, QMS, regulatory compliance, and documentation practices is mandatory.
- Strong communication and teamwork skills are preferred.
📑 Documents Required
Interested candidates must carry photocopies of the following documents:
- Updated CV and a recent passport-size photograph.
- Academic certificates (10th, 12th, Graduation, Post-Graduation).
- Offer letter, appointment letter, and current CTC breakup.
- Last 3 months’ salary slips from the current employer.
- Relieving letter from previous employers.
- PAN Card and Aadhaar Card (self-attested copies).
📧 Application Process
If you are planning to attend this walk-in interview, kindly email your updated resume to:
Please confirm your availability by replying with “YES” in the email subject line.
🌟 Why Choose Lupin Ltd?
Lupin Ltd is a globally recognized pharmaceutical leader with a strong focus on quality, innovation, and regulatory compliance. Joining Lupin gives you exposure to world-class manufacturing practices, challenging assignments, and excellent career growth opportunities in the pharmaceutical industry.
