Live opening · Posted 5 days ago

Senior Executive - Production (Drug Product)

Piramal Pharma · Indore, Madhya Pradesh, India (On-site)
Linkedin No
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At a glance

The key details from the original listing.

Posted 5 days ago
CompanyPiramal Pharma
LocationIndore, Madhya Pradesh, India (On-site)
Work modeNo
SourceLinkedin
Listed5 days ago

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About the role

Description supplied by the original job listing.

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Division
Piramal Critical Care
Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders.
PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management.
PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs.
For more details, please visit https://www.piramalcriticalcare.com/global/
Job Title
Senior Executive - Production (Drug Product)
Job Description
Senior Executive - Production (Drug Product)
Key Roles & Responsibilities: 1. To carryout filling and packing activities as per BFR, BPR & SOPs. 2. To follow & maintain current GMP standards in production area/activities. 3. To follow day-to-day production schedule and ensure to complete production activities (filling & packing) as per schedule. 4. To take & follow operating instructions for the shift activities from superior/Manger 5. If any abnormality found in production area / activities, authorized to stop activity immediately & highlight to production Manager. 6. To maintain manufacturing records online & should comply data integrity practices. 7. Verification of Raw material & Packing material during receipt. 8. Sample request/submission to QC after filling activity. 9. Transfer finished goods through “Finished Goods Transfer Note” to Stores.

Work arrangement
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