Job Description
Piramal Pharma is inviting applications for the role of Executive – TSD at Digwal, TS. This opportunity is with Piramal Pharma Solutions, a contract development and manufacturing organization offering end-to-end development and manufacturing solutions across the drug life cycle.
The Executive – TSD role is responsible for providing technical support and documentation for PPL Pharma Inc.’s products and processes within the Technical Services Department. The position supports regulatory compliance and contributes to the efficiency of pharmaceutical operations.
Job Details
| Company | Piramal Pharma |
| Division | Piramal Pharma Solutions |
| Position | Executive – TSD |
| Department | Quality Assurance |
| Location | Digwal, TS |
| Qualification | Bachelor’s degree in Chemical Engineering, or a related scientific discipline |
| Experience | 2-4 years |
Key Responsibilities
- Develop, revise, and maintain technical documentation, including batch records, Standard Operating Procedures (SOPs), protocols, and reports for pharmaceutical manufacturing processes.
- Provide technical support for manufacturing operations, including troubleshooting process deviations and implementing corrective and preventive actions (CAPAs).
- Participate in process validation activities, including authoring protocols and reports, and executing validation runs.
- Assist in investigating product quality issues, deviations, and customer complaints, including root cause identification and solution proposal.
- Collaborate with Manufacturing, Quality Assurance, Regulatory Affairs, and Research & Development teams to support project execution and regulatory compliance.
- Support the implementation of new technologies and processes with proper documentation and training.
- Stay updated with industry trends, regulatory requirements such as GMP and ICH guidelines, and best practices in pharmaceutical manufacturing and technical services.
- Conduct data analysis and generate reports to support process improvements and decision-making.
Qualification
- Bachelor’s degree in Chemical Engineering, or a related scientific discipline.
- Strong understanding of Good Manufacturing Practices (GMP) and other relevant regulatory guidelines such as ICH.
- Proven ability to author clear, concise, and accurate technical documentation.
- Experience with process validation, deviation investigation, and CAPA management.
- Excellent analytical, problem-solving, and written and verbal communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
- Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.
Experience
Candidates should have a minimum of 2-4 years of experience in a technical services, manufacturing, or quality assurance role within the pharmaceutical industry.
How to Apply
Interested candidates can apply online through the official Piramal Pharma careers link given below.
