standardizing biosample management, simplifying workflows, enabling scientific discoveries.

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Production Supervisor

Are you looking for an opportunity to have a direct impact on your company’s success through ingenuity, initiative, and collaboration? Accelerate your career development at GenVault, a rapidly growing start-up located in Carlsbad, CA. We develop and market defining technologies that enable room temperature storage and transport of biological samples for genomic discovery, medicine and identification. Our products are innovative, environmentally-friendly and continually evolving to become the industry standard. GenVault values and rewards open communication, integrity, and high performance. Don’t miss this exciting opportunity to launch your career. Send your resume to careers@genvault.com.

Benefits:

Health, dental, disability insurance, casual dress, 401(k) plan, much more

Primary Responsibilities

  • Supervise manufacturing operation to meet production requirements.
  • Develop, implement procedures and methods to ensure compliance with manufacturing goals, GMP regulations, Quality Assurance/Control requirements and safety requirements.
  • Ensure automated manufacturing equipment is properly running at full capacity and maintained to mitigate down time.
  • Ensure new employees are trained on safe and proper performance of their duties.
  • Perform hands on manufacturing tasks as needed based on demand.
  • Monitor production materials and manpower requirements to ensure sufficient assets to support demands.
  • Review and plan purchasing materials requirements.
  • Maintain the production and inventory control system.
  • Other operational responsibilities as required.

Required Qualifications

  • A minimum of 8 years’ industry experience manufacturing with a biotech, pharmaceutical or life science tools company with at least 3 years in a lead or supervisory position.
  • Experience in a GMP environment preferred.
  • Willingness to where multiple hats.
  • Experience with an automated manufacturing equipment.
  • Proven ability to maintain the documentation required in a GMP production environment.
  • Ability and interest in production planning and establishing resource requirements.
  • Ability to work in teams, multi-task, and work under deadlines.
  • Strong written and oral communication skills.