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Senior Manager of Quality Assurance
2 months ago
Kerry Search Partners
- Leading-edge organization
- Strategic management position
- Multi-location oversight
Overview of the Ideal Candidate
- Experience in client-facing roles.
- Proven strategic leadership (how to enhance our quality organization).
- Track record of developing and managing high-performing teams.
- Strong executive presence.
Are you an experienced quality management professional with a commitment to driving strategic initiatives and achieving significant outcomes? We invite you to join our esteemed global leader in healthcare and scientific solutions, where innovation is at the forefront.
Your Role: Senior Quality Manager - Site Quality Head
In this pivotal position, you will oversee the Quality department for the entire site. Your responsibilities will include fostering a customer-centric quality culture and implementing effective quality processes. This role emphasizes enhancing the customer experience through feedback and delivering products that meet the highest industry standards of quality.
Key Responsibilities:
- Establishes the Quality strategy for products in alignment with Division, Group, and Company objectives. Ensures effective implementation and execution of this strategy.
- Provides Quality leadership across a multi-site network.
- This role is expected to engage with customers, building professional relationships with their Quality counterparts.
- Ensures all product value stream interactions are aligned to deliver Quality products and processes.
- Facilitates resolution of quality issues as necessary and communicates effectively with senior leaders and diverse audiences.
- Utilizes Quality Risk Management to mitigate risks of failure modes that could affect the consistent supply of Quality products.
Qualifications:
- Bachelor's degree or higher in Science, Engineering, or related fields.
- Over 10 years of experience in the Pharmaceutical, Biotechnology, or Medical Device Industry, specifically with Regulated Products.
- Minimum of 2 years of experience managing a multi-site organization.
- Experience in audit (ISO9001 or similar) or inspection (FDA or similar) management.
- Expertise in Quality Management System design and oversight 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 meaningfully in a dynamic and innovative organization, we look forward to your interest.
