Piramal Enterprises is Hiring for Executive Lab QA and has issued notification to accept Applications.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. A global leader in integrated solutions, it offers a comprehensive range of services across the drug life cycle from drug discovery services and development to commercial manufacturing of drug substances and drug products. With accreditations from regulatory bodies in the US, Europe & Japan, its development centres and manufacturing sites across the globe, committed to research and development programs.. Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Executive Lab QA as follows.
Vacancy summary details :
- Company Name: Piramal Enterprises
- Location : Indore, Pithampur
- Post Name: Executive Lab QA
- Qualification: B.Pharma
- Experience:4 to 8 years of relevant experienceÂ
- No of Vacancies: NA
- Details of Salary: NA
- Closing date for online Application : Apply as soon as possible
- Mode of application : online
- Selection Process: Shortlisted candidates may called for selection process (Â Personal interview , Group discussion , etc…,)
- Contact : NA
Job Description/Skills Required:Â
- o ensure cGMP in Quality Control laboratory.
- Review of QC / QA documents.
- Review and approve OOS, OOT, and Incident and Stability data of QC Laboratory.
- To review and ensure effective implementation of regulatory requirement, guidelines and pharmacopeia changes like IP,BP,USP,Ph.Eur,JP etc.
- To review of QC laboratory records on periodic basis.
- To impart training to QC Laboratory personnel on SOPs, on-job training, regulatory requirements and guidelines.
- To ensure monthly back-up of software data of all QC instruments.
- To ensure compliance of AMC/PM visit for all QC instruments
- To ensure compliance of Qualification and calibration planner for QC instruments.
- To control and maintain QC Laboratory records (Issuance and archival of the documents like Laboratory note Book, Chromatograms, COA etc.).
- To provide Quest data on monthly basis to concern person.
- To perform self-audit of QC laboratory on periodic basis.
- To take the responsibilities of the activity in absence of immediate superior.
- To assign/disable password for QC laboratory analyst and to check audit trail in QC Instruments.
- To assign/disable password for QC Biometric system.
- Ensure compliance to KRAs and other such assignments.
- Analytical and Electronic data review of respective batches at the time of release.
- Involving in Self Inspection activity at Site.
- Document Submission/Regulatory submission to Customer regulatory department.
- Document Submission to PEL Corporate Regulatory Affairs (CRA).
- Â Â Support to site DICO (Data Integrity Compliance Officer) for monitoring and implementation of actions related to Data Integrity awareness at site.
