QUALITY VALIDATION SPECIALIST at Evolve Scientific
Melbourne, Melaka, Australia -
Full Time


Start Date

Immediate

Expiry Date

27 Nov, 26

Salary

0.0

Posted On

29 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

n this role, you will:

·       Provide ownership and execution of key QMS processes, including internal audits, supplier audits, deviations, OOS investigations, CAPA management, change controls, Annual Product Reviews and Quality Risk Management activities.

·       Lead complex Quality investigations and risk assessments, ensuring scientifically sound root cause analysis, impact assessment and effective corrective actions.

·       Coordinate the MAUS internal audit program, including planning, execution, reporting, follow-up activities and verification of effectiveness.

·       Manage supplier assurance activities, including supplier qualification, performance monitoring, audits, quality issue management and GMP Agreement administration.

·       Support inspection readiness, audit-ready Quality records and timely closure of Quality actions, while partnering with cross-functional teams across Quality, Regulatory, Manufacturing and Supply Chain.

·       Provide technical guidance, mentoring and practical Quality support the QA Associate to build help strengthen capability and deliver key Quality outcomes effectively, accountability and continuous improvement across the QA function.

Responsibilities
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