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Location

Clayton, NC | United States

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Job description

We are a globally recognized leader in diabetes care with a century-long history of innovation and commitment to helping improve the lives of people with diabetes and other chronic diseases. Our mission extends beyond delivering excellent healthcare solutions; we aim to provide life-changing opportunities for our employees and make a significant impact on global health.

In North Carolina, we boast three state-of-the-art pharmaceutical manufacturing sites, each playing a crucial role in our supply chain for injectable and oral treatments. Our Clayton facility is a prime example, specializing in the production of cutting-edge treatments for diabetes and obesity. Joining our team means becoming part of a worldwide network of professionals dedicated to making a difference.

What We Offer
Competitive salary and performance bonuses.
Generous PTO, including 14 paid holidays.
Comprehensive health, dental, and vision insurance from day one.
A guaranteed 8% 401K contribution with an additional match option.
Extensive family-focused benefits, including paid parental and family medical leave.
Complimentary access to our pharmaceutical products.
Tuition assistance and support for continuous learning.
Life and disability insurance.
Employee referral incentives.

The Role
As the Vice President of Quality Control, you will spearhead our Quality Control department, ensuring our products and devices meet and exceed all business, regulatory, and customer standards in line with our company values. You will oversee Chemistry, Microbiology, Physical Testing, and Raw Material testing, managing equipment, personnel, facilities, and budget. Your leadership will extend to supporting analysis for production sites and contract manufacturers.

Responsibilities
Strategize and manage Quality Control activities across our sites, fostering innovation and collaboration to enhance processes and quality.
Lead and develop a team of directors and managers, promoting a healthy and engaging work environment.
Play a pivotal role in the Senior Leadership Team, contributing to plant goals, continuous improvement projects, and policy setting.
Ensure the scientific integrity and GMP compliance of QC Laboratory data and operations.
Manage LIMS systems and laboratory equipment, ensuring timely results for batch releases and GMP compliance across the site.
Drive strategic change in culture and business positioning, addressing complex issues with sustainable solutions.
Oversee critical investigations to ensure effective preventive actions are implemented.
Develop and execute long-term business strategies and financial goals.
Physical Requirements
Office environment work with occasional travel (up to 10%).
Development of People
Foster individual development plans and career growth for your team, ensuring alignment with business priorities.

Qualifications
Bachelor's degree in Chemistry, Microbiology, or a relevant field; Master's degree preferred.
Over 12 years of quality experience in the pharmaceutical industry, with significant leadership and laboratory experience.
Demonstrated knowledge of Sterile Product cGMPs and API Production.
Proven ability in strategy development, implementation, and achieving impactful business results.

Our Commitment
We are devoted to an inclusive recruitment process and equal opportunity for all applicants. We celebrate diversity and are committed to creating an inclusive culture for all employees. We believe in being the best company for the world, driven by talented individuals from diverse backgrounds.

If you are driven to make a difference and ready to contribute to a life-changing mission, we welcome you to apply.
Employment Type: Full-Time
Salary: $ 158,000.00 Per Year

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