Director of Reagent Manufacturing Operations-MN
Listed on 2026-09-12
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Manufacturing / Production
Production Manager, Regulatory Compliance Specialist, Operations Management
Director of Reagent Manufacturing Operations-MN
MN
Required Experience:
- 5+ years’ experience managing complex manufacturing teams within an FDA/ISO-regulated industry.
Education:
- Bachelor’s degree with 14+ years’ experience or Master’s/Doctoral degree with 10+ years’ experience.
A global diagnostics and life sciences leader that focuses on the development and commercialization of in vitro diagnostic products seeks a Director of Reagent Manufacturing Operations for its Minnesota location.
The Director of Reagent Manufacturing Operations will be responsible for the manufacture and delivery of Immunoassays, including Reagent Operations, the Reagent Operations budget, and associated SQDC metrics. He/She will report to the Senior Director of Reagent Operations.
Knowledge & SkillsKey Duties, Activities and Responsibilities:
- Provide strategic and tactical leadership to the Reagent value stream to deliver products on time while meeting Safety, Quality, and Productivity objectives.
- Achieve KPIs for safety, quality, on-time delivery, inventory, and operational P&L.
- Generate budgets and control expenses related to labor, controllable expenses, and manufacturing variances.
- Hire, develop, and retain talent supporting site goals and customers’ expectations.
- Lead and collaborate worldwide, cross-functionally, to accomplish business objectives, ensuring material, quality systems, and technical support are available when needed.
- Lead the adoption of the company throughout Reagent Manufacturing to improve quality, delivery, cost, and innovation by applying tools and a continuous improvement mindset.
- Ensure strategies are communicated and well understood by the Team.
Work Experience, Skills and
Education Required:
- Bachelor’s degree with 14+ years’ experience or Master’s/Doctoral degree with 10+ years’ experience.
- 5+ years’ experience managing complex manufacturing teams within an FDA/ISO-regulated industry.
- Demonstrated proficiency in a DBS, Lean, or Six Sigma Culture and understanding of Lean manufacturing tools and concepts.
- Proven track record of working cross-functionally within matrixed organizations to achieve business outcomes.
- Experience managing budgets.
- Experience working with Oracle and electronic batch records.
- Travel, Motor Vehicle Record & Physical/Environment Requirements.
- Ability to travel 10% of time, internationally.
It would be a plus if you also possess previous experience in:
- Engaging and developing teams; driving succession and development of talent.
- Leading in a culture biased to action and accountability.
9897 Lake Worth Road, Suite 202
Lake Worth, FL 33467 USA
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