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Piramal Pharma

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306 Piramal Pharma Jobs

Senior Manager- Quality (DDRC)

17-19 years

Mumbai

1 vacancy

Senior Manager- Quality (DDRC)

Piramal Pharma

posted 6d ago

Job Role Insights

Flexible timing

Job Description

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

3.0
 Rating based on 1 Quality Manager review

Likes

HR policy and transportation services

  • Salary - Good
Dislikes

Higher Management and their control

  • Job security - Poor
  • +1 more
Read 1 Quality Manager review

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
53%
42%
52%
96%
Flexible timing
Monday to Saturday
No travel
Day Shift
View more insights

Piramal Pharma Benefits

Submitted by Company
Free Transport
Soft Skill Training
Job Training
Health Insurance
Submitted by Employees
Health Insurance
Free Transport
Job Training
Free Food
Soft Skill Training
Cafeteria +6 more
View more benefits

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Piramal Pharma Mumbai Office Location

View all
Mumbai, Maharashtra Office
Headquarter
Kamani Junction, LBS Marg, Piramal Ananta, Agastya Corporate Park, Kurla, Maharashtra 400070, IN Mumbai, Maharashtra
400070

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