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Manufacturing Supervisor

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Nuclein, LLC.
Full Time position
Listed on 2026-07-26
Job specializations:
  • Manufacturing / Production
    Regulatory Compliance Specialist, Operations Management, Lean Manufacturing / Six Sigma, Production Manager
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below

Position Summary:

The Manufacturing Supervisor will provide front-line support for Nuclein’s manufacturing operations. The individual will be responsible for overseeing day-to-day manufacturing activities, ensuring compliance with FDA regulations and GMP guidelines, and contributing to continuous improvement initiatives to optimize efficiency and product quality.

Essential Duties and Responsibilities:
  • Front-line support for Nuclein’s manufacturing operations, ensuring adequate resources, manufacturing capacity and planning as well as assisting in coordinating the direct labor and test technician operations
  • Follow and support required cGMP production processes and procedures.
  • Monitor production metrics and support corrective actions as needed.
  • Ensure strict adherence to FDA regulations and GMP guidelines through audits and daily oversight.
  • Help coordinate and develop training documentation and plans for assembly team members.
  • Collaborate with the Quality Assurance and Quality Control teams to address quality issues.
  • Help identify opportunities for process optimization and efficiency improvements.
  • Implement lean manufacturing principles to streamline operations.
  • Participate in and support continuous improvement projects.
  • Supervise and support a team of assembly personnel, and participate in the interviewing/hiring process as needed
  • Foster a culture of teamwork, accountability, and continuous improvement.
  • Participate in performance evaluations and provide coaching to team members.
  • Promote a safe working environment by enforcing safety protocols.
  • Investigate and report safety incidents, implementing preventive measures.
  • Monitor department costs and escalate concerns as appropriate
Education, Qualifications, and/or

Experience:
  • Associate’s degree required with bachelor’s degree preferred
  • At least 5 years of experience in manufacturing operations or equivalent role(s) required, preferably in the medical device industry
  • Experience operating in environments of FDA regulations and GMP guidelines required
  • Excellent problem-solving and decision-making skills.
  • Ability to support process improvements and contribute to cost reduction efforts.
  • Ability to work collaboratively, explain the ‘Why,’ and be able to influence others in a fast-paced environment.
  • Ability to operate with general supervision and escalate issues appropriately.
  • Ability to work cross-functionally to ensure all manufacturing objectives are met.
  • Possesses a high level of attention to detail and organization.
  • Ability to prioritize tasks and to delegate them when appropriate.
  • Experience in using/navigating ERP systems
  • Proficient with Microsoft Office Suite or related software to complete reports and logs.
Physical Requirements:
  • Repetitive Motion:
    Mostly computer use
  • Weight Lifting: at least 25 lbs
  • Position:
    Mostly sitting
  • Speaking and communicating
  • Occasional use of PPE may be required in laboratory/manufacturing/warehouse areas

LOCAL CANDIDATES ONLY- SPONSORSHIP IS NOT OFFERED AT THIS TIME

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