Lupin Walk-in Interview 2025.Lupin Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..
Vacancy details:
- ❇️Bachelor’s / Master’s degree in Pharmacy, Pharmaceutical Sciences, or related field.
- ❇️7– 8 years of experience in ophthalmic formulation development or sterile dosage forms.
- ❇️Strong understanding of cGMP, GDP, and regulatory frameworks (USFDA, EMA, etc.).
Important Details :
- Selection Process: The selection will be on the basis of Interview
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Description:
Greetings from Lupin..!!
We are Hiring for Executive – PDL (Process Devlopment Lab) at Lupin Limited, Pithampur.
📌Key Responsibilities:
❇️Demonstrate in-depth knowledge of manufacturing processes for ophthalmic dosage forms such as solutions, suspensions, and emulsions.
❇️Design and execute process development, optimization, and validation activities.
❇️Conduct scale-up, exhibit, and validation batches in alignment with project timelines and regulatory expectations.
❇️Maintain awareness of regulatory guidelines applicable to USA, EU, and other regulated markets.
❇️Ensure all development activities align with global regulatory standards and submission requirements.
❇️Prepare and review scale-up protocols, batch manufacturing records (BMRs), and technical reports.
❇️Ensure adherence to Good Documentation Practices (GDP) and internal quality systems.
❇️Collaborate effectively with cross-functional teams including R&D, QA, RA, and manufacturing.
❇️Utilize SAP and other quality system software for documentation, batch tracking, and data management.
Interested candidates can share their profiles at 📧 suhailkhan1@lupin.com
📌 Subject Line: Executive – PDL
We are Hiring for Officer – Validation (Hormonal Plant) at Lupin Limited, Pithampur.
🎓Qualifications & Skills:
❇️Bachelor’s degree in Pharmacy.
❇️2– 6 years of experience in formulation.
❇️Strong understanding of Validation & Regulatory frameworks (USFDA).
📌Key Responsibilities:
❇️Cleaning Validation: Handle protocol/report preparation, acceptance criteria, and tracking of cleaning verification activities.
❇️Equipment Qualification: Prepare, review, and execute FAT, IQ, OQ, PQ; review URS, DQ, SAT, and vendor documents.
❇️HVAC & Utility Qualification: Execute and document qualifications for AHUs, HEPA filters, water, steam, compressed air, nitrogen, etc.
❇️Packaging Validation: Conduct and document packaging validation activities including data compilation and report preparation.
❇️Facility Qualification: Manage facility qualification tasks and related documentation.
❇️Cross-Functional Coordination: Collaborate with QA, QC, Engineering, Production, and external vendors for validation activities.
❇️Documentation: Prepare/review SOPs, Validation Master Plans, study protocols/reports, and qualification status labels.
❇️Compliance & QMS: Handle change controls, deviations, CAPAs, and ensure adherence to SOPs and requalification timelines.
❇️Training: Participate in training and mentor team members as required.
Interested candidates can share their profiles at 📧 suhailkhan1@lupin.com
📌 Subject Line: Officer – Validation
ABAC
