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Division
Piramal Pharma Solutions
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Executive-Production
Job Description
Responsible for supervising and performing day-to-day production activities in SPPS Production, ensuring adherence to established standards, safety protocols, and regulatory compliance. The role encompasses workforce allocation, raw material issuance, work permit management, and maintenance of production-related documentation including BMR and BECR records, with a focus on quality, efficiency, and process consistency.
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Supervise and perform day-to-day production activities in SPPS Production
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Ensure all processes are carried out as per established standards and timelines.
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Monitor the production floor for quality, safety, and efficiency.
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Distribute work assignments among workmen as per operational requirements.
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Allocate manpower based on skill sets and production priorities.
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Issue raw materials as per production requirements with accurate documentation.
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Monitor and minimize raw material wastage during production.
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Issue and maintain all production-related documents in a timely manner.
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Ensure adherence to regulatory and internal documentation standards.
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Handle and process work permits in compliance with applicable safety protocols.
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Ensure all activities are duly authorized prior to commencement.
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Review and verify executed Batch Manufacturing Records (BMR) and Batch Equipment Cleaning Records (BECR)
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Ensure accuracy, completeness, and regulatory compliance of all reviewed records.
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Monitor and control cleaning activities on the production floor.
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Ensure BMR-BECR documentation is maintained with precision and consistency.
