Piramal Released Job Openings On 27/07/2022.Piramal Enterprises Limited is the Contract Development and Manufacturing Organisation (CDMO) business division of Piramal Enterprises Limited, with operations in North America, Europe and Asia.Â
Vacancy Details:
Piramal Recruiting B.Sc,B.Pharma,M.sc Graduates with 03-07 Years of Experience for Quality Assurance Consultant ( On contract – 6 months ).Position
Important Details :
- Location : Mumbai
- Details of Salary:NA
- Opening date for online Application: 27/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job: Cipla Hiring FRESHERS – Email Resume
Job Description/Skills Required
- 1) Timely issuance of Documents as Document Controller; issuance to CPD team members without any reminders
- 2) 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
- 3) 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
- 4) 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
- 5) Timely PTL Payment and Invoice clearance; without any reminders from them, this will support business relations
- 6) 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
- 7) Efficient Ensure Management (Document Management System), as system owner; this will help us keeping effect and LIVE documents at all times
- 8) Visit to sites for Quality audits if required
- 9) Review and audit of Raw data of Third Party sites
- 10) Coordinate with Public Test Labs, CFAs, TP sites for samples
- 11) Review BMR/ BPRs/ RM and PM specifications
Experience:
Looking for women applicants who are on career sabbatical/break and would to restart their career.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.
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