What are the responsibilities and job description for the Supervisor, Consumable Manufacturing position at Accelerate Diagnostics Inc?
Job Summary: The Consumable Manufacturing Supervisor will oversee the production of reagents and consumables at Accelerate Diagnostics. This role is responsible for supervising a team of manufacturing technicians, ensuring adherence to safety and quality standards, and maintaining efficient production processes. The supervisor will collaborate with cross-functional teams to troubleshoot production issues, optimize workflows, and ensure compliance with regulatory guidelines.
Key Responsibilities:
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Supervision & Leadership:
- Lead, train, and manage a team of manufacturing technicians in the preparation and production of reagents and consumables.
- Schedule and prioritize work to meet production targets while ensuring high-quality standards.
- Conduct performance evaluations and provide feedback, coaching, and development opportunities for team members.
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Production & Process Management:
- Oversee the day-to-day production of reagents and consumables, ensuring that all batches are produced accurately, efficiently, and in compliance with standard operating procedures (SOPs).
- Monitor production schedules and adjust workflows to meet deadlines.
- Identifies scheduling conflicts, production issues and collaborates with support functions for resolution
- Ensure proper documentation of manufacturing processes, batch records, and related activities in accordance with company policies and regulatory standards.
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Inventory & Equipment Management:
- Oversee raw material inventory levels and ensure timely ordering and replenishment to prevent production delays.
- Ensure proper maintenance and calibration of manufacturing equipment.
- Coordinate with procurement and quality control teams to maintain supply chain integrity.
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Quality Assurance & Compliance:
- Ensure that reagents are manufactured in compliance with relevant regulatory standards (e.g., FDA, ISO).
- Enforce good manufacturing practices (GMP) and maintain a clean and safe work environment.
- Conduct regular inspections and audits to ensure product quality and process adherence.
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Problem Solving & Continuous Improvement:
- Troubleshoot production issues and resolve bottlenecks or delays to ensure smooth operation.
- Identify areas for process improvement and implement best practices to enhance production efficiency and product quality.
- Participate in root cause analysis and corrective action processes for any quality or production issues.
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Education:
- Bachelors degree in scientific discipline (e.g., Biology, Chemistry, Biochemistry, or a related field).
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Experience:
- Minimum of 7 years of experience in a manufacturing environment, preferably in reagent or chemical production. Reagent bulk formulation experience required.
- At least 1-2 years of supervisory or leadership experience.
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Preferred Skills:
- Strong knowledge of manufacturing processes, quality control, and regulatory requirements (e.g., GMP, ISO, FDA).
- Excellent communication, leadership, and team management skills.
- Critical thinking, problem solving and a can-do attitude are required
- Proficient in using manufacturing software such as QAD, and Microsoft Office tools.
- Demonstrated ability to develop and lead a high-performing team
- Proven skills and experience with process improvement and Lean manufacturing
- Proficient written, verbal communication and presentation skills
- Demonstrated ability to make data-driven decisions
Physical Requirements:
- Ability to lift and move materials up to 50 pounds.
- Ability to stand for extended periods and work in a manufacturing environment.
Work Environment:
- Work is primarily conducted in a manufacturing facility with exposure to chemicals, laboratory equipment, and machinery. Safety protocols must be strictly followed.
- Shift Hours: 6:00 am-2:30 pm
Additional Information:
- Occasional overtime may be required based on production needs.
- This position may require flexibility in shift work, including weekends or holidays.