203 Piramal Pharma Jobs
Deputy Manager - Quality Assurance
Piramal Pharma
posted 28d ago
Flexible timing
Key skills for the job
Job Overview
The incumbent will be responsible to ensure that all external and internal processes and systems are followed before our product reaches our customers. Would be responsible for inspecting procedures, review QMS documents and outputs and identifying non-conformity issues.
Location
Zirakpur Punjab
Reporting Structure
This role will report to Chief Manager - QA
Experience
Minimum 3-7yrs in QA/ QC/ Microbiology, experience of working at shop floor as IPQA/QC/ monitoring TP sites, experience in auditing formulation manufacturing sites is desirable.
Roles & Responsibilities
Timely issuance of Documents as Document Controller; issuance to CPD team members without any reminders • Keeping updated repository of all documents and related trackers; like CCF, Deviation, Specs, STPs etc. with complete document records and File Management; Documents to be closed as per timelines and all files and to be serially numbered with complete indexing • Handling of market complaints as L0 level in SamVaad and Complaint Samples tracking and Analysis; timely focus on this activity will help us to improve CRS score to positive • PTL (Public Testing Lab) Sample, Analysis and Report Management, with updated trackers; timely availability of quotations, and coordinating and tracking PTL teams performance for report issuance will help us to improve and commit testing timelines and projects • Timely PTL Payment and Invoice clearance; without any reminders from them, this will support business relations • Management of Shared Folder and common folder and efficient Archival System (soft as well as Hard Copies); ensuring timely availability of documents within the team at all times • Efficient Ensure Management (Document Management System), as system owner; this will help us keeping effect and LIVE documents at all times • Visit to sites for Quality audits if required • Review and audit of Raw data of Third Party sites • Coordinate with Public Test Labs, CFAs, TP sites for samples • Review BMR/ BPRs/ RM and PM specifications • Ensure validation activities related to PEL products, as per compliance • Document management for TP sites • Daily reporting to Chief Manager - Quality of PPL
Employment Type: Full Time, Permanent
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