Job Title:
Senior Executive – Technical Services Department (TSD)
Location:
Ennore, Tamil Nadu (Onsite)
Employment Type:
Full-Time
Department:
Technical Services Department (TSD)
Division:
Piramal Pharma Solutions
About Piramal Pharma Solutions
Piramal Pharma Solutions is a leading Contract Development and Manufacturing Organization (CDMO) offering integrated solutions across the pharmaceutical product lifecycle. With a global presence across North America, Europe, and Asia, the company provides services in drug discovery, process development, clinical trial supplies, API manufacturing, and finished dosage forms for innovator and generic pharmaceutical companies worldwide.
For more details, visit: Piramal Pharma Solutions
Job Summary
We are seeking an experienced and result-oriented Senior Executive – TSD to provide technical support for pharmaceutical manufacturing operations. The role involves process validation, technology transfer, process optimization, troubleshooting manufacturing issues, and ensuring compliance with regulatory standards.
The ideal candidate should possess strong technical expertise in pharmaceutical manufacturing processes and demonstrate the ability to work collaboratively with cross-functional teams to achieve operational excellence and product quality objectives.
Key Responsibilities
Lead and execute process validation activities, including protocol preparation, execution, and report generation for new and existing products.
Provide technical support and troubleshooting assistance for manufacturing operations.
Investigate process deviations and implement effective Corrective and Preventive Actions (CAPAs).
Support technology transfer activities from R&D to commercial manufacturing.
Conduct process optimization studies to improve yield, productivity, cycle time, and product quality.
Collaborate with Production, Quality Assurance (QA), Quality Control (QC), and R&D teams for smooth project execution.
Prepare, review, and maintain technical documents such as batch manufacturing records, SOPs, specifications, and validation reports.
Support regulatory submissions by providing required technical data and documentation.
Ensure compliance with cGMP, ICH guidelines, and other applicable regulatory requirements.
Participate in investigations related to OOS results, quality events, and customer complaints.
Stay updated with industry trends, best practices, and advancements in pharmaceutical technologies.
Required Qualifications
Bachelor’s Degree in Chemical Engineering.
5–8 years of experience in Technical Services, Process Development, or Manufacturing within the pharmaceutical industry.
Required Skills & Competencies
Strong knowledge of pharmaceutical manufacturing processes, including APIs, sterile injectables, and solid oral dosage forms.
Expertise in process validation, technology transfer, and process optimization.
Good understanding of cGMP, ICH guidelines, and regulatory compliance standards.
Strong analytical, problem-solving, and troubleshooting abilities.
Effective communication and cross-functional collaboration skills.
Ability to manage multiple projects and priorities in a fast-paced environment.
Work Mode
Onsite – Ennore, Tamil Nadu
Application Deadline
Applications close on May 31, 2026.
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