Manager- Quality (DDRC) Micro

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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.

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Job Title

Manager- Quality (DDRC) - Micro

Job Description

Job Description JOB OVERVIEW: The role entails providing remote support for the Quality Management System (QMS) and reviewing microbiology data for Piramal Pharma Limited (PPL) sites. Key responsibilities include overseeing Out of Specification (OOS) investigations laboratory incidents deviations and change controls as well as reviewing data generated in the microbiology laboratory. Additional duties involve drafting and reviewing documentation ensuring adherence to regulatory standards and recommending ongoing improvements. KEY STAKEHOLDERS: INTERNAL Site Quality Team (QC QA) Corporate Functions EXTERNAL Regulators (during inspection) Solution Providers REPORTING STRUCTURE: PPL Site Quality (Functionally) and CQA Document Data Review & Creation (Administratively) Key ResponsibilitiesReview any microbial data generated in the microbiology Review microbiological and analytical data generated in labs including entries in Open-Lab lab notebooks LIMS and QMS modules. Ensure accuracy and completeness in the review and generation of reports. Prepare and review OOS OOT and lab incident investigations ensuring thorough analysis and initiation of change controls. Review planned and unplanned deviations for accuracy completeness and compliance with cGMP data integrity and written procedures. Review protocols reports and Annual Product Quality Reviews (APQR). Collaborate with site teams to identify and address gaps during QMS event reviews and documentation. Coordinate with sites for review activities and planning to ensure efficient workflows. Engage with customers and site teams to ensure timely closure of critical QMS events. Share review deficiencies with site teams for corrective actions. Route documents through the Ensur application (or other relevant platforms) across Piramal plants. Participate in customer audits and regulatory inspections providing support to site teams. Lead and participate in additional tasks or projects as assigned by the Head of Department (HOD). Essential QualificationQUALIFICATION: B. Pharm / M. Pharm / . Chemistry / . Chemistry or equivalent/Microbiology EXPERIENCE: Need to be ready to live and embrace the Piramal values. Quality professional with 10 years of QC/QA experience in regulated pharmaceutical companies. Hands-on experience reviewing microbial data generated in microbiology laboratories. Skilled in reviewing OOS OOT and lab incident investigations as well as initiating and managing deviations and change controls. Experience in reviewing Annual Product Quality Reviews (APQR). Strong knowledge of regulatory requirements including USFDA EU and Health Canada. Proficient in current Good Laboratory Practices (cGLP) and use of QC instrumentation. Demonstrated experience coordinating with customers and site management teams for effective QMS closure. Well-organized detail-oriented and committed to maintaining high-quality standards. Excellent verbal and written communication skills. effective team player with strong collaboration skills.