Senior Executive - TSD

Be the First to Apply

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

Senior Executive - TSD

Job Description

The Senior Executive - TSD will be responsible for providing comprehensive technical support for pharmaceutical manufacturing processes, ensuring product quality, process efficiency, and regulatory compliance.

• Lead and execute process validation activities, including protocol generation, execution, and report writing for new and existing products.
• Provide technical expertise and troubleshooting support for manufacturing operations, resolving deviations, and implementing corrective and preventive actions (CAPAs).
• Participate in technology transfer activities for new products and processes from R&D to commercial manufacturing.
• Conduct process optimization studies to improve yields, reduce cycle times, and enhance product quality.
• Collaborate with cross-functional teams including Production, Quality Assurance, Quality Control, and R&D to ensure seamless execution of projects.
• Prepare and review technical documents, including batch records, specifications, and standard operating procedures (SOPs).
• Support regulatory submissions by providing necessary technical data and documentation.
• Stay updated with industry best practices, regulatory guidelines (e.g., cGMP, ICH), and new technologies in pharmaceutical manufacturing.
• Participate in investigations of critical quality events, out-of-specification (OOS) results, and customer complaints.

Job Qualifications

• Bachelor's degree in Chemical Engineering.
• 5-8 years of experience in a Technical Services, Process Development, or Manufacturing role within the pharmaceutical industry.
• Strong understanding of pharmaceutical manufacturing processes (e.g., solid oral dosage forms, sterile injectables, APIs).
• Proficient in process validation, technology transfer, and process optimization principles.
• Familiarity with cGMP, ICH guidelines, and other relevant regulatory requirements.

Chemical Engineering