QC Jobs at Piramal | Chemistry Graduates Apply Now
Are you looking for QC jobs, MSc Chemistry jobs, or Chemistry Graduate jobs in a leading pharmaceutical company? The Manager – Quality (DDRC) role at Piramal offers an excellent opportunity to work with a globally trusted organization known for innovation, integrity, and scientific excellence. This position is ideal for experienced professionals seeking growth in analytical review, quality compliance, and cGMP-driven operations.
About Piramal
Piramal Enterprises is a global business conglomerate with diverse interests in pharmaceuticals, financial services, healthcare insights & analytics, and real estate. Committed to excellence and customer satisfaction, our pharmaceutical division leverages innovation and cost-effective solutions to deliver quality products. Join us to be part of a leading company where innovation, collaboration, and integrity drive success. This opportunity is ideal for candidates seeking QC jobs, MSc Chemistry jobs, and Chemistry Graduate jobs in a reputed organization.
Job Description
Provide remote analytical support to PPL sites, including review of analytical data and preparation of documents such as specifications, test methods, and protocols. Upload documents for review in ENSURE and initiate QMS elements in TrackWise/eDMS. Prepare and review stability protocols and reports, and perform stability data trending and analysis.
Responsibilities
- Review of analytical data generated in the analytical lab (QC/AS), including but not limited to IPC, raw materials, intermediates, finished products, cleaning verification/validation, stability, and method validation data according to cGMP, GDP, in a timely manner.
- Review of reports for accuracy and completeness. Reports may include, but not be limited to: method validation reports, stability reports, lab equipment and instrumentation Calibration and Preventive Maintenance (PM) Reports, etc.
- Ensure compliance with the internal approved procedures, specifications, and protocols of all generated data.
- Review all planned and unplanned deviations for accuracy, completeness, and compliance with data integrity, written procedures, and CGMP regulations.
- Release raw materials and intermediate products, based upon conformance with specifications and completion of associated documents.
- Analytical/Microbial data review in Empower/Chromeleon/Open-Lab/Lab-Notebooks/LIMS/QMS module and activity signoff per site procedures.
- Data reviewed virtually or on-site in Empower/Chromeleon/Open-Lab/Lab-Notebooks/LIMS, etc., whenever required across the Piramal plants.
- Share the review deficiencies with the site team for further action.
- Preparation of Specification, Test procedure, Analytical Protocol, and Analytical Report as per site procedure.
- Create/review the LIMS master built whenever required across the Piramal plants.
- To coordinate with the site for review activities/planning.
- Routing the documents in the Ensur application (or any application mode) whenever required across the Piramal plants.
- To participate and support the site during customer audits and regulatory inspections.
- Lead and participate in any other task assigned by the HOD.
Qualifications
B. Pharm / M. Pharm / M.Sc. Chemistry / B.Sc. Chemistry or equivalent.
- Job Identification: 8773
- Apply Before: 12/30/2025, 05:13 AM
- Degree Level: Bachelor’s Degree
- Job Schedule: Full-time
- Locations: Project: Piramal Agastya, PRL Agastya Pvt Ltd., LBS Marg, Kamani Junction, Mumbai, Maharashtra, 400070, IN
