QC Supervisor

Oxoid Remel Microbiology (Acquired from Thermo Fisher Scientific); Lenexa (KS); Presencial; USD 85 000 - 105 000; Tempo integral

Resumo da oferta

Oxoid Remel Microbiology is seeking a Quality Control Supervisor to lead the daily operations of the Lenexa laboratory. You will manage a team of 6–10 QC staff, drive continuous improvement, ensure compliance with FDA, GMP, and CLSI/USP guidelines, and partner across functions to resolve quality issues.

The role requires hands-on leadership, strong microbiology knowledge, and the ability to develop personnel while maintaining safety and efficiency.

Qualificações

• Bachelor's degree in Biological Sciences, with Microbiology preferred.
• Minimum 5 years of microbiology laboratory experience.
• 2–5 years of supervisory or people-management experience.
• Experience leading technical laboratory personnel and investigations.

Responsabilidades

• Lead the daily activities of the Quality Control laboratory, establishing priorities and assigning work.
• Manage, coach, train, and develop a team of approximately 6–10 Quality Control employees.
• Ensure laboratory activities comply with SOPs, FDA requirements, GMP, and quality standards.
• Investigate out-of-limit results, deviations, and product failures, including root cause analysis.

Conhecimentos

Microbiology

Leadership

Quality control

Problem solving

Communication

MS Office

Formação académica

Bachelor’s degree in Biological Sciences (Microbiology preferred)

Ferramentas

SAP

Descrição da oferta de emprego

Joining Oxoid Remel Microbiology, you’ll play an active part in helping deliver products that support accurate disease identification, targeted treatment, and microbiology testing around the world. Our teams are committed to quality, reliability, and continuous improvement, helping ensure customers receive products they can depend on.

As a Quality Control Supervisor, you’ll lead the day-to-day activities of our Quality Control laboratory in Lenexa, Kansas. You’ll oversee and develop a team of QC professionals, ensure products and testing activities meet established quality and regulatory requirements, and partner across functions to investigate issues and continuously improve laboratory performance.

This is a hands‑on leadership opportunity for someone who combines a strong microbiology laboratory background with people leadership, problem‑solving, and a commitment to quality.

About the Role

The Quality Control Supervisor is responsible for the daily operations of the Quality Control laboratory, including product testing, product disposition, employee development, laboratory performance, and compliance with established procedures and applicable regulatory requirements.

You’ll lead a team of approximately 6–10 Quality Control employees and work closely with Quality, Manufacturing, Operations, and other cross‑functional partners. The role will also support investigations, new product and process introductions, continuous improvement initiatives, and laboratory safety.

This position is based in Lenexa, Kansas, and typically works Monday through Friday. Flexibility to work overtime and weekends when business needs require is essential.

What You Will Do

• Lead the daily activities of the Quality Control laboratory, establishing priorities and assigning work to ensure testing and product disposition activities are completed effectively and on schedule.
• Manage, coach, train, and develop a team of approximately 6–10 Quality Control employees, including performance management and ongoing technical development.
• Ensure laboratory activities are performed in accordance with established Standard Operating Procedures, FDA requirements, Good Manufacturing Practices (GMP), and applicable quality standards.
• Develop, document, implement, and maintain Quality Control procedures and testing practices.
• Investigate out‑of‑limit and unexpected test results, deviations, and product failures, including root cause analysis, risk assessments, and corrective actions.
• Collaborate with cross‑functional teams to develop testing plans for new products and update existing testing methods in alignment with applicable CLSI and USP guidelines.
• Ensure timely review and disposition of finished goods to support business and customer needs.
• Lead the integration of new products, equipment, testing methods, and processes into the laboratory.
• Apply continuous improvement and Lean principles to improve laboratory efficiency, quality, and performance.
• Develop and maintain visual management tools and key performance indicators to provide visibility to laboratory performance and critical priorities.
• Lead 5S and standard work initiatives to maintain an organized, efficient, and compliant laboratory environment.
• Support the Quality Control Manager by monitoring departmental expenses against budget.
• Communicate critical testing priorities, backorders, risks, and laboratory status through daily management processes.
• Promote a strong safety culture through routine Gemba walks, employee engagement, and proactive identification and resolution of laboratory safety concerns.
• Partner effectively across departments to resolve quality and testing issues and support broader site and business priorities.

What You Will Bring

Minimum Qualifications

• Bachelor’s degree in Biological Sciences or a related scientific discipline, with Microbiology strongly preferred.
• Minimum of 5 years of microbiology laboratory experience.
• 2–5 years of supervisory or people‑management experience, including direct responsibility for employees.
• Demonstrated experience leading and developing technical laboratory personnel.
• Strong understanding of laboratory testing practices, investigations, deviations, root cause analysis, and problem‑solving.
• Ability to effectively manage multiple priorities in a fast‑paced environment while maintaining strong attention to quality and detail.
• Strong interpersonal and collaboration skills with the ability to work effectively across departments.
• Strong organizational, analytical, critical‑thinking, and decision‑making skills.
• Excellent written and verbal communication skills in English.
• Proficiency with Microsoft Office, including Word, Excel, and PowerPoint.
• Ability and willingness to work overtime and weekends when business needs require.

Preferred Qualifications

• Experience working in an FDA‑regulated medical device, diagnostic, or similarly regulated environment.
• Familiarity with Good Manufacturing Practices (GMP), USP, and CLSI requirements.
• Experience with SAP.
• Experience working on cross‑functional teams and supporting new product, equipment, or process introductions.
• Experience with Lean, continuous improvement, 5S, standard work, or visual management methodologies.
• Experience preparing project reports, tracking departmental metrics, and supporting budget management.

What Will Help You Succeed

You’ll be well positioned for success in this role if you are a hands‑on leader who enjoys being close to the laboratory and your team. You can balance multiple priorities, make thoughtful decisions when issues arise, and take ownership through resolution.

You’ll also bring a collaborative approach, strong follow‑through, and the flexibility to support the team when business needs require additional hours. Most importantly, you’ll create an environment where quality, safety, accountability, and continuous improvement are part of how the team operates every day.

Join Us

This is an exciting opportunity to join Oxoid Remel Microbiology and lead a Quality Control team supporting products that play an important role in microbiology and diagnostic testing.

You’ll have the opportunity to develop people, strengthen laboratory operations, partner across functions, and lead improvements that directly influence product quality, operational performance, and our ability to serve customers.

If you’re an experienced microbiology laboratory professional who enjoys leading teams, solving complex problems, and creating a culture of quality and continuous improvement, we’d love to hear from you.