Job Description
The JD is given below:
Role : LIMS Specialist - Master Creation/An enduser
Designation : Sr.Associate |
Exp - 3 to 10 Years
Shift Timing - 12 PM - 9PM1. Create and revise CofAs and revise Analytical Test Methods in the corporate document management system due to ongoing change control activities.
2. Create and revise laboratory documentation for solid dosage, liquid dosage and raw material products to support Global and cross-site product transfers to apply common harmonized testing policy for laboratories.
3. Issue document numbers for new CofAs and analytical test methods.
4. Route electronic documents in LIMS and Document Management Systems to secure the history and allow items to become available to subsequent users for re-editing purposes in a controlled environment.
5. Update appropriate Global databases and Change Management Systems to reflect revision history for revised laboratory documents.
6. Ensure the timely distribution of lab documentation to the appropriate laboratories & external customers by posting to the intranet or via physical distribution.
7. Monitor ApoWeb document collections for CofAs and analytical test methods to ensure that electronic versions for viewing purposes are current.
8. Collaborate with internal customers to resolve laboratory documentation issues.
9. Develop and maintain effective working relationships with internal customers.
10. Load basic product specifications into LabWare LIMS, with Supervision.
11. Develop and maintain detailed working knowledge of corporate document, change and laboratory management system through all software upgrades.
12. Track all work using designated tracking systems and process.
13. Perform all work in compliance with current SODs and GMPs.
14. Participates in department projects as required.
15. Works as a member of a team to achieve all outcomes.
16. Performs all work in support of our Corporate Values of Pride, Accountability, Integrity and Diligence; Demonstrates strong and visible support of our values.
17. Performs all work in accordance with all established regulatory and compliance and safety requirements.
18. All other duties as assigned.
Interested candidates share your updated CVs to
ar***t@bv**c.comEmployement Category:
Employement Type: Full time
Industry: Pharma / Biotech
Role Category: R&D / Product Design
Functional Area: Not Applicable
Role/Responsibilies: LIMS / eLab - Pharma MNC - Mumbai (Shift12pm
Contact Details:
Company Name: BVR eopleLocation(s): Mumbai