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Qa Product Release Coordinator Jobs in Indiana

Sap Ns2 Director Of Qa & Release Management - Virtual
By SAP At , Newtown Square, 19073
Minimum of 10 years of experience in Quality Assurance and Release Management, with at least 5 years in a leadership role.
Develop and manage the release management process, ensuring that all releases are planned, tracked, and executed efficiently.
Deep understanding of quality assurance practices and a strong background in release management and release cycles.
Strong knowledge of SAP cloud offerings.
All internal transfers must have manager’s approval.
Manage high volume and high risk/complex projects, ensuring that they are delivered on time and within budget.
Qa Project Coordinator Jobs
By Planet Pharma At Albany, New York Metropolitan Area, United States
Quality assurance or document/ records management experience (must be clear on resume)
Archival of batch documentation in an electronic document management system.
Cultivates own working knowledge of QA & the roles within a cGMP environment.
Performs other administrative support responsibilities as requested.
Responsible for documentation support for QA Department staff
Tracks status and timelines of QA record review/approval and QA lot disposition.
Qa Batch Release Technician
By Novartis At , Indianapolis, In $57,000 - $85,600 a year
Controlled issuance of batch records in preparation for manufacturing.
Perform review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately.
Assist functional areas with achieving timely and compliant final product disposition of the product.
Ensure Specifications in place and are within GMP compliance.
Organize and file all executed and associated GMP documentation (e.g. batch records).
Maintain batch documentation library (record check-in, check-out, follow-up, and distribution).
Qa Batch Release Specialist
By Novartis At , Indianapolis, In $92,800 - $139,200 a year
CAPA management as well as improving processes within QA Batch release.
Proven track record and practical experience with cGMP requirements.
Knowledge of FDA and EU regulations and experience in US and international regulatory agency inspections.
2+ years of experience in a GxP Biopharmaceutical manufacturing operations. 1+ years of experience in a quality assurance role.
QA and QC experience in biotech pharmaceutical biotechnology industry with environmental monitoring & cleanliness zones is desired.
Your responsibilities include, but are not limited to: