Director of quality Audit,systems,compliance / Pharma / Up to $14,000/month! - Innovative Company

My client, a rapidly expanding pharma company is looking out for a Director of quality audit,systems and compliance.

Details of the roles as mentioned below:

Role Objectives:

 Lead a team of Quality professionals overseeing global aspects of Quality Audit, Systems, and Compliance.

• Ensure compliance with relevant competent authorities and company standards.
• Oversee internal quality compliance of business stakeholders with the Company’s Quality Management System worldwide.

Role Responsibilities:

Leadership in Change and Transformation:

• Identify and pursue continuous improvement opportunities within the Quality Management System, including electronic Quality Management Systems (eQMS) and other quality IT systems.
• Provide clear guidance to the global prescription products operations team to align quality operations with business objectives.
• Establish and maintain a risk-based and effective approach to quality operations.

Team Management:

• Review staff performance plans regularly to track progress against agreed objectives.
• Measure and enhance productivity of the QA team, reporting progress to executive management through metrics.
• Empower team members to take ownership of their roles and responsibilities, fostering a sense of accountability for business success.
• Direct operations of the QA Audit, Systems, and Compliance Group.

Collaboration and Stakeholder Management:

• Act as an integral member of the Quality Ops Leadership team.
• Represent the function in key quality governance meetings and collaborate with the organization to fulfil quality activities.

Additional Skills and Attributes:

• Minimum 10 years of experience in the Life Sciences, Pharmaceutical, or Consumer Healthcare industries.
• Strong background and expertise in quality management with a focus on overall business requirements.
• Experience in leading site audits, with at least 5 years of audit experience as Lead Auditor, preferably certified by an industry-recognized body such as ASQ.
• Knowledge of GMP/ISO standards, international regulations, and industry best practices in a manufacturing environment.

How to Apply:

Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:

Consultant: Tan Jun Jie

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