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306 Piramal Pharma Jobs
Senior Manager- Quality (DDRC)
Piramal Pharma
posted 4d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
Business: Piramal Pharma Solutions
Department: Quality
Location: Kurla
Travel: Low
Job Overview
Remote support to PPL sites in reviewing analytical data remotely, preparing master build in LIMS (Lab Vantage / Labware), Document Preparation (specifications, test methods, protocols, etc. ) and uploading for review in ensure, initiating QMS elements in Trackwise / eDMS.
Key Stakeholders: Internal
Site Quality Team (QC, QA), Corporate Functions
Key Stakeholders: External
Regulators (during inspection), Solution Providers
Reporting Structure
PPL Site Quality (Functionally) and CQA Document, Data Review & Creation (Administratively)
Qualification:
B. Pharm / M. Pharm / M. Sc. Chemistry / B. Sc. Chemistry or equivalent/Microbiology
Experience
Need to be ready to live and embrace the Piramal values.
Quality professional with 12+ years of QC / QA experience in a regulated pharma companies.
Must have hands-on experience in Laboratory softwares, testing, applications and systems (Chromatography By HPLC and GC, UV, IR, Dissolution, Malvern, KF auto titrator, etc).
Must have worked in LIMS for Data entry / master build, and data review.
Knowledge of applicable regulatory requirements / regulations (USFDA, EU, Health Canada, others).
Need to be aware of latest regulations and pharmacopeial requirements.
Well-organized and committed, with strong verbal and written communication skills. Good Collaboration skills and Team player.
Key Roles and Responsibilities:
Supervise and manage the preparation of Master Builds in LIMS, ensuring the timely and accurate completion of all related tasks, including analytical data review, compendia assessments, document preparation, and uploading.
Oversee track-wise operations for QMS activities.
Lead the preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents, ensuring they meet regulatory and internal requirements.
Operational knowledge of eDMS and ensure application compliance.
Monitor compendial changes and prepare evaluation reports (including specifications and methods) for affected site products and materials.
Review analytical data, raw data, chromatography, and LIMS for RM/PM/FP.
Prepare and review new SOPs.
Ensure timely completion of documentation.
Maintain data integrity while preparing, uploading, or reviewing documents.
Collaborate effectively across Piramal Plants.
Provide support to any PPL site as required, with role assignments based on evolving needs and timelines.
Perform activities across US, Canada, and EU time zones; available to travel for up to 3 months to PPL sites (India and overseas) as needed.
Perform additional tasks as assigned by the Leadership team based on requirements
B. Pharm / M. Pharm / M. Sc. Chemistry / B. Sc. Chemistry or equivalent/Microbiology
Employment Type: Full Time, Permanent
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What people at Piramal Pharma are saying
Rating based on 1 Quality Manager
review
Anonymous · Other
in Hyderabad / Secunderabad
Likes
HR policy and transportation services
- Salary - Good
Dislikes
Higher Management and their control
- Job security - Poor
+1 more
Quality Manager salary at Piramal Pharma
reported by
4
employees
with 14-17
years exp.
₹11.2
L/yr - ₹16.4
L/yr
11%
more
than the average Quality Manager Salary in India
View more details
What Piramal Pharma employees are saying about work life
based on 966 employees
Flexible timing
Monday to Saturday
No travel
Day Shift
Piramal Pharma Benefits
Submitted by Company
Free Transport Soft Skill Training Job Training Health Insurance
Submitted by Employees
View more benefits 
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Piramal Pharma Mumbai Office Location
Mumbai, Maharashtra Office
Headquarter
Kamani Junction, LBS Marg, Piramal Ananta, Agastya Corporate Park, Kurla, Maharashtra 400070, IN
Mumbai, Maharashtra
400070
400070
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