Software Quality Assurance Director directs and oversees the implementation of policies and procedures for the software quality assurance function. Evaluates and monitors tools, methodologies, and automation to ensure effective testing and identification of defects. Being a Software Quality Assurance Director oversees user acceptance, alpha, and beta testing efforts. Requires a bachelor's degree. Additionally, Software Quality Assurance Director reports to top management. The Software Quality Assurance Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a Software Quality Assurance Director typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
Job Title : Quality Associate
Duration : 12 Months (Possibilities of extension)
Location : Durham, NC 27709 (Onsite)
Job Description :
Ø Activities include but are not limited to a review of GMP raw data for compliance.
Ø The QA Associate II will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental, and human resources policies and procedures and adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers.
Ø Review and approval of batch related documentation (Solution Lot records, Reports, Logbooks and Release of Autoclaved Equipment) to support product disposition.
Ø Transport batch related documentation across RTP buildings to support chain of custody and life cycle management.
Ø Supports resolution of both technical and compliance issues / gaps of mild to moderate complexity.
Ø Assists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by Client.
Ø Complete and maintain related GMP training.
Ø Additional job duties that may be assigned from time to time.
Required :
Ø 0-2 years directly related to position responsibilities or biologic experience preferred.
Last updated : 2024-02-25
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