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Quality Assurance Site Leader

2 months ago

Provo, Utah, United States Kerry Search Partners Full time

Kerry Search Partners

  • Leading-edge technology
  • Strategic leadership role
  • Multi-site management

Ideal Candidate Profile

  1. Experience in client-facing roles.
  2. Proven track record in strategic quality improvement.
  3. Expertise in developing and managing high-performance teams.
  4. Strong executive presence and communication skills.

Are you an experienced quality management professional passionate about implementing strategic initiatives and achieving significant outcomes? Join our esteemed global organization specializing in healthcare and scientific solutions, where innovation and purpose converge.

Your Role: Senior Quality Manager - Site Quality Head

In this pivotal position, you will oversee the Quality division for the entire site. Your responsibilities will include fostering a customer-centric quality culture and establishing robust quality processes. This role emphasizes enhancing customer satisfaction through feedback and ensuring the delivery of products that meet top-tier industry quality standards.

Key Responsibilities:

  • Formulates the Quality strategy for products in alignment with Division, Group, and Company objectives, ensuring effective implementation.
  • Provides Quality leadership across a multi-site network.
  • Engages with customers, establishing professional relationships with their Quality counterparts.
  • Ensures alignment of all product value stream interactions to deliver high-quality products and processes.
  • Facilitates resolution of quality issues and communicates effectively with senior leadership and diverse audiences.
  • Employs Quality Risk Management techniques to mitigate risks that could affect the consistent supply of quality products.

Qualifications:

  • Degree in Science, Engineering, or related fields.
  • Over 10 years of experience in the Pharmaceutical, Biotechnology, or Medical Device sectors, focusing on Regulated Products.
  • A minimum of 2 years leading a multi-site organization.
  • Experience in audit (ISO9001 or similar) or inspection (FDA or similar) management.
  • Proficient in designing and overseeing Quality Management Systems from a pharmaceutical or medical device perspective.
  • Familiarity with compliance to quality standards (e.g., 21 CFR Part 820, 21 CFR Part 11, ISO 13485, 9001).

If you are prepared to advance your career and contribute to a dynamic and innovative organization, we look forward to your interest.