5 дней назад
Laboratory Supervisor (Acute Systems)
88 000 - 121 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Laboratory Supervisor (Acute Systems) (Medical Devices): Leading safe, compliant, and efficient laboratory operations for verification, validation, controls, and product development at a research center with an accent on equipment readiness, materials management, and regulated laboratory practices. Focus on coordinating laboratory personnel and vendors, improving workflows through continuous-improvement methods, and maintaining audit-ready quality and safety systems.
Location: Plymouth, Minnesota, United States; minimum 3 days per week onsite
Salary: $88,000–$121,000 annually, with potential discretionary bonus eligibility
Company
develops vital organ therapy solutions, with a focus on kidney care, dialysis, digital solutions, advanced services, and medical-device innovation.
What you will do
- Lead the safe, compliant, organized, and efficient operation of Acute Systems R&D laboratories supporting product development, verification, and validation.
- Coordinate laboratory personnel, workspaces, equipment, materials, facility expansions, installations, and workspace modifications.
- Develop laboratory procedures, checklists, operating mechanisms, readiness metrics, and continuous-improvement initiatives.
- Manage equipment calibration, maintenance, qualification, troubleshooting, repairs, inventories, consumables, vendors, and service agreements.
- Partner with Quality, Employee Health and Safety, Facilities, Calibration, and laboratory users to maintain inspection-ready operations.
- Supervise and develop laboratory support personnel through prioritization, coaching, technical guidance, cross-training, and coverage planning.
Requirements
- Associate degree in engineering, engineering technology, biomedical technology, electronics, mechanical technology, laboratory science, or a related technical discipline.
- Relevant experience supporting or managing an engineering, R&D, test, verification and validation, service, or regulated laboratory environment.
- Experience coordinating people, equipment, materials, vendors, and competing priorities, as well as improving procedures and workflows.
- Working knowledge of equipment maintenance, calibration coordination, inventory control, workplace safety, and technical documentation.
- Strong organizational, written communication, interpersonal, ownership, and follow-through skills.
- Ability to work primarily onsite in a hands-on laboratory environment; the flexible workplace policy requires at least 3 days per week onsite.
Nice to have
- Bachelor’s degree in engineering, engineering technology, biomedical engineering, operations, laboratory science, or a related field.
- Five or more years of relevant laboratory, technical, engineering-support, or operations experience.
- Previous supervision of technicians or technical support personnel.
- Experience in medical devices, life sciences, pharmaceuticals, or other regulated product-development environments.
- Experience with design verification and validation, medical-device quality systems, audit readiness, nonconformance management, corrective and preventive actions, and electromechanical medical-device troubleshooting.
Culture & Benefits
- Hands-on, collaborative work supporting patient-focused vital organ therapies.
- Medical, dental, and vision coverage beginning on day one for eligible roles.
- 401(k) retirement savings plan, investment resources, financial education, and educational assistance.
- Paid holidays, 20–35 days of paid time off based on service length, family and medical leave, and paid parental leave.
- Life, disability, business travel accident, commuting, childcare, employee assistance, and employee discount benefits.
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