About The Position

The Quality Control, 2nd Shift Supervisor manages team operations to ensure drug products meet high quality and safety standards through disciplined testing and data analysis. This role is responsible for organizing stability studies and delivering timely results to support manufacturing demands. Additionally, the supervisor fosters a professional, safe work environment while handling complex technical problems and non-routine assignments.

Requirements

  • Bachelor's degree in a scientific field, with a preference for Microbiology or Biochemistry; A combination of education and years of experience will be considered
  • 5-10 years of cGMP experience and 2+ years direct supervisory experience
  • Experience in applicable laboratory software and hardware systems
  • Use of GMP Quality Systems such as: TrackWise, LIMS, DMS, Electronic note book
  • Excellent ability to prioritize work load for group and problem solve
  • Proactively shares knowledge with others and encourages analyst development
  • Troubleshoot assay and instrumentation issues involving data mining, trending and analysis to identify problems

Nice To Haves

  • Advanced Graduate degree (M.S./Ph.D.)

Responsibilities

  • Scheduling, planning and assurance of on-time delivery of routine testing in compliance with all cGMP and regulatory requirements
  • Ensures a safe work environment for employees to perform their duties
  • Creating, reviewing and approving QC documentation
  • Implementation of robust laboratory management systems, continuous improvement and enhancement of existing systems in a coordinated effort to reduce deviations
  • Schedule and attend department and site related meetings to assure delivery, to quality systems, continuous improvement and customer satisfaction
  • Drive all projects to on-time completion be ensuring task completion and communicating potential issues to stakeholders
  • Troubleshooting and resolving these issues through team efforts
  • Resolving personnel issues and workplace conflicts
  • Establishing a cohesive team environment that focuses on achieving corporate goals and right first time initiatives
  • Leading OE initiatives, continuous improvements, implementation of new processes and procedures to support site and corporate growth, hiring and mentoring of staff, support regulatory and customer audits, create and execute CAPA plans
  • Perform other duties as assigned

Benefits

  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Competitive salary and performance-based bonuses
  • 401(k) matching plan
  • Competitive compensation programs that reward high performance
  • Comprehensive medical, dental, and vision insurance
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service