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Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry, has a proud, historical track record going back one hundred years. With a turnover in excess of Rs. 3000 crores today, Alembic Pharmaceuticals Limited is one of the leading API & Formulations manufacturing and marketing pharmaceutical company. We continue to enjoy leadership positions in antibiotics, anti-infective, anti-cough, and also have a significant worldwide presence in specialty therapeutic areas such as cardiology, neurology, diabetology, etc.
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We have newly setup plants of Oncology, General Injectable, and Dermaceuticals. Upcoming plans of General Oral Solid Dosage at Jarad, near Vadodara. Alembic is having manufacturing facilities at Vadodara, Panelav, Karkhadi, Jarod in Gujarat, and Domestic manufacturing of Formulations at Sikkim. Gujarat based facilities are approved by the US FDA, EDQM, TGA, MHRA, and MCC. Alembic Research Center at Vadodara (ARC) and AG Research Center at Hyderabad a world-class research organization provides a comprehensive range of services in the areas of synthetic chemistry, formulations, NDDS, Oncology as also preclinical pharmacology, bioequivalence / bio-analytical studies, etc. ARC & AG Research, designed to state-of-the-art GLP standards with more than 350 scientists working on the latest technology and systems. Our current employee strength is in excess of 8000 across the country. A continuously expanding organization, we invite dynamic, result-oriented competent personnel to join us across various functions
Alembic Pharmaceuticals is looking for competent personnel to be an integral part of our team for USFDA approved API plant-based at Karakhadi in Vadodara, Gujarat.
Position:Â Executive/Sr Executive Validation Lab – Reviewer & Documentation
Location: Karakhadi, Vadodara, Gujarat
Job Description
CVL-Reviewer & Documentation
- Thorough knowledge of RS, Assay, Residual solvent, and PSD method validation as per ICH guidelines.
- Expert in analytical raw data review for method validation, method transfer, and instrument calibration.
- Aware of cGMP practices, must follow and maintain GLP.
- Experience in GLP activities such as instrument installation and qualification.
- Knowledge of regulatory requirements.
- Knowledge of cinematographic software Empower 3.
- Able to maintain all Lab records, logbooks, calibration data, SOPs, training records, etc.
- The applicant should be comfortable working at the plant location.
Qualification: B.Sc/B.Pharma/M.Pharma/MS/M.Sc
Experience: 3-7 Years
Salary: Negotiable
Contact Details:
Ms. Samiksha Upadhyay
Ph: +91265-300 8105 M.+918866081543
samiksha.upadhyay@alembic.co.in, researchcareers@alembic.co.in, talent@alembic.co.in
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