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Walk-In for R&D Documentation Officer

Walk-In for R&D Documentation Officer

Leben Life Sciences is hiring R&D (Analytical Development Laboratory) Officers in Documentation at its EU-GMP certified facility in Akola. Walk-in on July 27, 2025. Apply now to advance your pharmaceutical career in GLP & cGMP-compliant documentation.

Leben Life Sciences Walk-In Drive – R&D Documentation Officer | 27th July 2025 in Akola

Are you an experienced pharmaceutical documentation professional looking for your next big opportunity? Leben Life Sciences Pvt. Ltd., a trusted pharmaceutical formulation company with over four decades of legacy, is conducting a Walk-In Interview for R&D (Analytical Development Laboratory) Officer – Documentation at its EU-GMP-approved facility in Akola, Maharashtra, on 27th July 2025.

🌐 Why Choose Leben Life Sciences?

Founded in 1980, Leben Life Sciences has been at the forefront of responsible healthcare, offering high-quality formulations across therapeutic segments like anti-infectives, gastroenterology, dermatology, and pain management. With its state-of-the-art R&D and manufacturing facility certified by EU-GMP, Leben is committed to regulatory excellence and innovation in oral solid dosage (OSD) and semi-solid formulations.

🗓️ Walk-In Interview Details

  • Date: 27th July 2025 (Saturday)
  • Time: 9:30 AM onwards
  • Venue: Leben Life Sciences Pvt. Ltd.,
    Plot No. C-20/1 & C-21, Phase III, MIDC, Akola, Shivar, Maharashtra – 444104
  • Pre-Registration: Scan the QR code on the official website or call 7498035480

👨‍🔬 Job Role: Officer – R&D Documentation (Analytical Development Laboratory)

Qualifications: M.Sc (Chemistry), B.Pharm, or M.Pharm
Experience: Minimum 1 year in R&D documentation (pharmaceutical industry)
Key Skills: GLP, cGMP, HPLC data handling, analytical method documentation

Responsibilities:

  • Prepare, review, and maintain analytical documentation in compliance with regulatory requirements.
  • Collaborate with the ADL team to ensure data integrity and audit readiness.
  • Support method development documentation for HPLC and related instrumentation.
  • Ensure alignment with GLP, cGMP, and EU-GMP standards.

📌 Eligibility Criteria

  • Minimum 60% marks in highest degree (First Class) OR
  • At least 5 years of relevant experience (Second Class)
  • Not eligible if interviewed within the last 3 months

🗂️ Documents to Carry

  • Updated resume
  • Educational certificates (original and photocopies)
  • PAN & Aadhar cards
  • Latest 3 months’ salary slips & CTC breakup

📩 How to Apply

If you’re unable to attend the walk-in, send your resume to career@lebenlifesciences.com. For queries, call 7498035480.
Note: Leben Life Sciences does not charge any recruitment fees—beware of fraudulent hiring agents.

🌟 Join a Legacy of Innovation

By joining Leben Life Sciences, you become part of a company that values integrity, innovation, and continuous learning. This is your opportunity to contribute to global healthcare and work in a regulatory-compliant, EU-GMP-certified facility with experienced pharmaceutical professionals.

Written by Pasupuleti

Empowering Aspirations: Your Ultimate Guide to Career and Academic Excellence.

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