Lupin Recruitment-Send Resume TO HR Mail

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