Executive - Documentation (Prod. Dept.)
5 months ago Engineering Palghar 25 views Reference: 33786Job Details
- To Handled all QMS documents as per cGMP guidelines.
- Preparation of new BPR, ECR, formats, SOPs and protocols its review and execution.
- To ensure all raw materials receipt, Solvent receipt and Verification.
- Co- ordinate with other department personnel for smooth operation of manufacturing activities.
- To plan and conduct process development batches as per technology transfer document.
- To maintain and check batch production records and other record on daily basis.
- To ensure operation procedure and instruction required for production.
- Handling of the deviation, OOS,OOT and incidents its investigation.
- To provide training to workers and shop floor officer of cGMP.
- To perform and check calibration activity, PM activity as per scheduled.
- To ensure facility and documents all time in presentable manner.
- To prepare and ensure reconciliation record and MIS report.
- To Keep plant updated in terms of GMP.
- Please Contact - Pranav Patil
Company Description
Aarti Pharmalabs Limited (APL) is an established, internationally recognised manufacturer of Active Pharmaceutical Ingredients (API), pharmaceutical intermediates, New Chemical Entities (NCE), and xanthine derivatives situated in India. In order to build a sustainable future, we integrate process chemistry proficiency (recipe focus) with scale-up engineering proficiency (asset utilisation).
Over the past two decades, enabled by cutting-edge R&D and manufacturing capabilities APL has evolved as a reliable partner of choice for generic players and innovators across the globe. We specialise in generic APIs, generic intermediates, and xanthine derivatives. We deliver CDMO services for drug substance/NCE development and manufacturing for innovative pharmaceutical and biotech firms with a focus on the Ph-I/II/III, launch, and commercial phases. We have dedicated facilities for the production of HPAPIs, corticosteroids, cytotoxic medicines, and oncology products.
With the biggest manufacturing capacity in India for our flagship product Caffeine APL has emerged as a preferred partner for the Beverages, Nutraceuticals manufacturing companies, and Pharmaceuticals Industries across the world.
Over the past two decades, enabled by cutting-edge R&D and manufacturing capabilities APL has evolved as a reliable partner of choice for generic players and innovators across the globe. We specialise in generic APIs, generic intermediates, and xanthine derivatives. We deliver CDMO services for drug substance/NCE development and manufacturing for innovative pharmaceutical and biotech firms with a focus on the Ph-I/II/III, launch, and commercial phases. We have dedicated facilities for the production of HPAPIs, corticosteroids, cytotoxic medicines, and oncology products.
With the biggest manufacturing capacity in India for our flagship product Caffeine APL has emerged as a preferred partner for the Beverages, Nutraceuticals manufacturing companies, and Pharmaceuticals Industries across the world.
