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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 carrying out production documentation activities in compliance with cGMP, EHS, and quality requirements to ensure safe, efficient, and timely manufacturing as per the production plan.
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Prepare, review, and maintain Batch Manufacturing Records (BMR) and production documents.
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Ensure documentation complies with cGMP, GDP, and data integrity requirements.
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Initiate and coordinate Change Controls for production-related activities.
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Perform Quality Risk Assessments (QRA) and implement risk mitigation actions.
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Investigate deviations, incidents, and quality events, and support root cause analysis (RCA) and CAPA.
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Review completed BMRs for accuracy and submit them to QA for batch release.
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Prepare and revise SOPs, formats, and production-related documents.
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Coordinate with QA, QC, Engineering, and other functions for timely closure of quality documents.
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Ensure timely closure of Change Controls, investigations, CAPAs, and risk assessments.
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Support internal, customer, and regulatory audits by maintaining audit-ready documentation.
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Identify and implement documentation and process improvements.
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Ensure compliance with cGMP, EHS, and company quality standards at all times.
Qualification:
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B.Sc. / M.Sc. in Chemistry or Diploma / B.E. in Chemical Engineering
Experience:
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2–8 years of experience in API, Intermediate, Chemical manufacturing with exposure to cGMP-compliant production operations.
