Zimmer Biomet · 8 hours ago
Senior Quality Manager
Zimmer Biomet is a global medical technology leader focused on enhancing patient mobility. The Senior Quality Manager will direct the quality function at a medical device design and manufacturing site, developing and implementing quality strategies, metrics, and leading a QA/QC team to ensure compliance and improve operational efficiencies.
Health CareManufacturingMedical DeviceProduct Design
Responsibilities
Develop and implement site-wide quality strategy aligned with corporate objectives and regulatory requirements (QMSR, GMP, ISO, and other global standards) including objectives, and planning to support the strategy
Establish and refine key quality metrics, ensuring data-driven decision-making to enhance product integrity and regulatory compliance
Partner with R&D, supply chain, manufacturing, and distribution teams to enhance quality processes across the product lifecycle and drive cross-functional teamwork to improve operational efficiencies, ensuring seamless integration of quality in all aspects of pharmaceutical production
Serve as the primary quality representative during regulatory inspections and audits, ensuring adherence to industry and corporate standards
Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team, fostering a culture of collaboration and accountability
Empower team to lead investigations into deviations, CAPA (Corrective and Preventive Actions), and change control processes to improve operational resilience and ensure timely product release and market supply by resolving quality-related issues effectively
Qualification
Required
Must have a thorough knowledge of QMSR, GMP, ISO and other relevant regulatory requirements as applied to medical device development, manufacturing and distribution
Demonstrated independent decision-making ability applying regulations and standards related to the manufacturing and distribution of medical device products
Demonstrated management ability including organizational design and employee selection, development, motivation and performance
Demonstrated ability to achieve productivity goals collaboratively without sacrificing quality in a manufacturing environment
Demonstrated understanding of interactions and interdependency of elements within the quality system in a pharmaceutical manufacturing organization
Must be able to work with all levels of employees, including hourly production employees through senior management
Must possess excellent written and oral communication skills and the demonstrated ability to communicate with individuals of varying backgrounds
A Bachelor's Degree in a technical field is required
7-10 years of work experience in medical device quality, preferably in manufacturing environments
5 years' experience with direct management responsibility
Preferred
CQE/CQM preferred
Benefits
Development opportunities
Robust employee resource groups (ERGs)
Flexible working environment
Location specific competitive total rewards
Wellness incentives
Culture of recognition and performance awards
Company
Zimmer Biomet
Zimmer Biomet is a medical device manufacturing company that offers orthopedic reconstructive, spinal, and trauma devices.
H1B Sponsorship
Zimmer Biomet has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2020 (2)
Funding
Current Stage
Public CompanyTotal Funding
$2.75B2025-02-20Post Ipo Debt· $1.75B
2016-12-14Post Ipo Debt· $1B
2001-08-03IPO
Leadership Team
Recent News
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2025-12-19
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