Senior Executive – Quality Control (QC)
Location: Navi Mumbai, Maharashtra, India
Industry: Pharmaceutical Manufacturing | CDMO
Function: Quality Control / Analytical Operations
Employment Type: Full-Time
Travel Requirement: Low
Job Overview
Piramal Pharma Solutions (PPS) is seeking a skilled Senior Executive – Quality Control (QC) to support analytical testing, stability studies, and cGMP-compliant documentation at its Navi Mumbai facility. The role involves hands-on analysis of in-process, intermediate, hold-time, and stability samples, preparation of stability protocols and reports, and ensuring compliance with internal quality systems and global regulatory standards.
The position also requires the ability to independently manage delegated responsibilities and support laboratory operations in the absence of the reporting authority.
Key Responsibilities
Quality Control & Analytical Testing
Perform analysis of in-process samples in accordance with approved SOPs and cGMP guidelines.
Conduct sampling and testing of intermediate samples as per in-house procedures and regulatory requirements.
Execute stability sample analysis, including charging, withdrawal, and testing as per approved protocols.
Analyze hold-time study samples and document results accurately.
Stability Studies & Documentation
Prepare, review, and maintain stability protocols, trend reports, and study summaries.
Ensure complete and accurate analytical documentation in compliance with cGMP, data integrity, and internal quality systems.
Maintain laboratory records, worksheets, and logs as per regulatory expectations.
Compliance & Operational Support
Support quality compliance by ensuring adherence to SOPs, safety guidelines, and laboratory best practices.
Handle delegated responsibilities of the reporting authority during their absence.
Perform additional QC-related tasks as assigned by senior management.
Education & Experience Requirements
Educational Qualifications
Bachelor’s or Master’s degree in Chemistry or a related scientific discipline.
Experience
3 to 6 years of relevant experience in Quality Control within a pharmaceutical manufacturing, API, or CDMO environment.
Hands-on experience in in-process analysis, stability studies, and GMP documentation is required.
Key Skills & Competencies
Strong knowledge of cGMP, GLP, and data integrity principles.
Experience with stability studies, hold-time studies, and analytical testing workflows.
High attention to detail and strong documentation practices.
Ability to work independently and collaboratively in a regulated laboratory environment.
Good communication and coordination skills.
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a global Contract Development and Manufacturing Organization (CDMO) offering integrated solutions across the pharmaceutical value chain. With a presence across North America, Europe, and Asia, PPS delivers expertise in APIs, peptides, highly potent compounds, biologics, sterile fill-finish, ADCs, and finished dosage forms. Its strong scientific capabilities and compliance-driven culture make PPS a trusted partner to pharmaceutical innovators worldwide.
Equal Employment Opportunity
Piramal Group is an Equal Employment Opportunity and Affirmative Action employer. All employment decisions are based on merit, qualifications, skills, and performance, without discrimination on any legally protected basis.
Apply Now
Apply through thepharmadaily.com to advance your career in pharmaceutical quality control and analytical sciences with a globally recognized CDMO.
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