Quality Lab Senior Supervisor

BaxterMarion, NC
Onsite

About The Position

This is where your creativity addresses challenges. You are creative, thorough, and a heads-down do-er. You embrace a challenge and truly apply the collaborative powers of your team to produce extraordinary results. You are motivated by work that is never the same from one day to the next. As a Senior Quality Lab Supervisor, you are unafraid of navigating through vital internal processes to facilitate a product you deeply believe in. You can absorb and act on sophisticated procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality. The position is directly responsible for operations and personnel within the Bioburden and Micro ID labs. In addition, the position is adjacently responsible for leadership activities to support all Microbiology Laboratory operations occurring on night shift.

Requirements

  • B.S. Degree in Life Science Field (e.g. Biology, Microbiology, related)
  • Minimum of 5 years of experience or Master’s Degree in biological science with applied experience, preferably in the pharmaceutical or medical device industry
  • Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs, and USP testing methodology
  • Computer skills including knowledge of Microsoft office applications (Word, Excel)
  • Able to manage multiple tasks/priorities in a timely manner
  • Able to work independently and manage time to complete assigned tasks
  • Ability to create an environment that values people, encourages trust, and open communication through feedback and recognition
  • Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

Responsibilities

  • Coordinate all activities required to occur for assigned shift responsibilities relative to the QC Laboratory including but not limited to: Personnel management
  • Conducting non-conformance investigations within TrackWise 8 for procedural non-compliances and non-conforming results
  • Assign tasks, set priorities, and ensure effective performance and development of team members
  • Conduct regular training for staff
  • Conduct ACE Check-ins with staff and additional communications as needed
  • Ensure testing is performed accurately and efficiently, following established protocols and standards
  • Oversee the accurate recording and analysis of test results, review results, and address documentation errors in accordance with procedural requirements
  • Ensure results are provided to document control within specified timeframes for release
  • Cross train in all areas of the QC Microbiology Laboratory which has staffing represented on night shift to enable troubleshooting of issues and/or guidance as necessary
  • Perform documentation review of all areas of QC Microbiology Laboratory as assigned by the Quality Manager
  • Troubleshoot and resolve any issues that arise during testing or lab equipment
  • Conduct Phase 1 Laboratory investigations for other areas of the laboratory as needed
  • Ensure that all data is documented properly, and reports are generated and reviewed in a timely manner
  • Implement and enforce safety protocols and practices within the laboratory

Benefits

  • Shift flexibility to trade shifts and leverage overtime opportunities
  • Medical, Dental and Vision coverage
  • 160 hours of Paid Time Off and Paid Holidays
  • 401K match
  • Employee Stock Purchase Program
  • Paid Parental Leave
  • Tuition Reimbursement
  • basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Flexible Spending Accounts
  • educational assistance programs
  • commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • childcare benefits
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