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Job Title: Insource Seninor Manager Quality Assurance APAC, R&D Quality Assurance
Job Location: Taiwan or Malaysia
Job Overview:
Our mission in Quality Assurance is to achieve enduring excellence in auditing, quality management, quality risk assessment and enhance the R&D quality mindset for the benefit of our patients.
The job holder is responsible for:
Planning, leading, conducts and reports audit activities for R&D GxP risk-based audit programs
Support of GxP inspection activities
Management of CAPAs related to audit and/or inspection findings in collaboration with QA colleagues and functions owning the issues.
Responsibilities:
Audit
Plans, leads, conducts and reports audits in assigned GxP areas, such as investigator site and/or project audits
Supports lead auditors in the planning, conduct and reporting of more complex audits such as Process / System, External supplier
Works with contract personnel or consultants to prepare, conduct and report outsourced audits
CAPA
Assesses need for, and assists in development of CAPA plans, approves and monitors plans to completion for assigned audits
Assists with the continuing follow-up of agreed audit CAPA actions from across QA to assist in the monitoring of QA Key Performance Indicators
General Accountabilities
Ensures own tasks are performed to current practices and in accordance with company policies, standards, SOPs and guidelines
Promotes a culture of ethics, integrity and continuous improvement that focuses on delivering efficiencies and planned business benefits
Communicates effectively with QA colleagues and business stakeholders
Maintains knowledge of relevant industry information affecting quality and compliance arena
May provide responsive and proactive quality and compliance advice to defined customers.
Support quality and compliance risk management for functional area using risk framework standards to define risk and develop mitigation recommendations
Travel expected
Requirements:
Essential
Degree level education or equivalent experience
Experience in pharmaceuticals or a related industry
Excellent analytical, written and oral communications skills
Fluent in written and spoken English
High ethical standards, trustworthy, operating with absolute discretion
Collaborative, influencing and interpersonal skills curious to understand business environment
Skilled at managing & using technology
Ability to develop professional networks with stakeholders
Desirable
Audit Experience
Supplier qualification
Experience of regulatory health authority GxP Inspections
Job ID: 135892367