Director of quality Audit,systems,compliance

2 weeks ago


Singapore INTEGRITY PARTNERS PTE. LTD. Full time
Roles & Responsibilities

Seeking a Director of Quality Audit, Systems, and Compliance for a thriving pharma company.

Role Objectives:

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

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

Role Responsibilities:

Leadership in Change and Transformation:

  • Identify and pursue continuous improvement opportunities within the Quality Management System, including electronic Quality Management Systems 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.
  • 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 the provided contact person or apply directly.

Consultant: Tan Jun Jie

EA personnel reg. no.R1878852

EA License No. 17C8502

Tell employers what skills you have

Healthcare Industry
Leadership
Quality Management
Quality Management Systems
ISO
Auditor
MS Word
Compliance
Team Management
Audits
Life Sciences
Stakeholder Management
Manufacturing
Audit
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