Description

The Assay Production Supervisor - Accellix is responsible for leading daily manufacturing operations for the Accellix product line. This role oversees production personnel, ensures products are manufactured safely and efficiently, and drives performance against quality, delivery, and productivity goals. The Production Supervisor partners with Quality, Engineering, Maintenance, and Planning teams to support continuous improvement and ensure compliance in a GMP-regulated environment.

Key Responsibilities

Production Leadership

• Lead and coordinate daily production activities to meet safety, quality, delivery, and productivity targets.
• Monitor production schedules and adjust resources to support operational priorities.
• Ensure manufacturing processes are executed efficiently and in accordance with established procedures.
• Address production issues promptly and escalate concerns as needed.

People Leadership

• Supervise, coach, and develop manufacturing technicians.
• Provide performance feedback, training, and development opportunities.
• Support staffing, cross-training, and workforce planning activities.
• Foster a culture of accountability, teamwork, safety, and continuous improvement.

Quality & Compliance

• Ensure adherence to GMP, GDP, quality system requirements, and company procedures.
• Support investigations, corrective actions, and audit readiness activities.
• Verify production records and documentation are complete, accurate, and compliant.
• Promote quality standards that support reliable product performance.

Continuous Improvement

• Monitor key performance indicators and identify opportunities for improvement.
• Partner with Engineering and Quality teams to improve manufacturing processes and operational efficiency.
• Support process transfers, validation activities, and new product introductions.
• Drive adherence to standard work and operational discipline.

Cross-Functional Collaboration

• Partner with Quality Control, Engineering, Maintenance, Supply Chain, and Planning teams to support production objectives.
• Help ensure alignment between production output, inventory requirements, and testing needs.
• Communicate production status, challenges, and improvement opportunities to leadership.

Qualifications

Required

• High School Diploma or equivalent required.
• 6+ years of experience in a lab-based manufacturing, biotechnology, pharmaceutical, medical device, or other regulated production environment. Including 2+ years Previous experience leading or coordinating production teams.
• Experience working with production metrics, quality systems, and manufacturing documentation.

Preferred

• Bachelor's degree in Engineering, Life Sciences, Manufacturing, Operations Management, or a related field.
• Reagent formulation or biomolecules
• Drying / stabilization processes
• Microfluidics or consumable manufacturing

Knowledge, Skills & Abilities

• Strong leadership and team development skills.
• Ability to prioritize work and manage multiple production activities.
• Effective problem-solving and decision-making skills.
• Strong communication and collaboration abilities.
• Ability to analyze production performance and drive operational improvements.
• Working knowledge of GMP and quality system requirements.
• Proficiency with Microsoft Office applications and manufacturing systems.

Working Conditions

• Combination of production floor and office environment.
• Ability to stand and walk for extended periods.
• Ability to wear required PPE in manufacturing areas.
• Occasional lifting and material handling as needed.
• Flexibility to support production activities outside of normal business hours when required.

The estimated wage range for this role based in Illinois is between $31.30 – 45.10. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux’s bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate’s experience and will be presented in writing at the time of the offer. 

In addition, bioMérieux offers a competitive Total Rewards package that may include: 

·        A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options 

·        Company-Provided Life and Accidental Death Insurance 

·        Short and Long-Term Disability Insurance 

·        Retirement Plan including a generous non-discretionary employer contribution and employer match. 

·        Adoption Assistance 

·        Wellness Programs 

·        Employee Assistance Program 

·        Commuter Benefits 

·        Various voluntary benefit offerings 

·        Discount programs 

·        Parental leaves 

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BioMérieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant’s identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMérieux’s or its affiliates’ application process by contacting us via telephone at (385) 770-1132, by email at [email protected], or by dialing 711 for access to Telecommunications Relay Services (TRS).