Advantage Technical
Research and Development Supervisor
Skills
11 days ago
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Important information
Contract type:
Freelance / Contract
Location:
St Paul, MN, USA
Work mode:
Onsite
Published on:
14 October 2026
What they need
R&D Supervisor
Onsite
Advantage Technical is seeking an experienced R&D Supervisor for a potential temp-to-perm opportunity supporting a fast-paced medical device organization.
This position is ideal for a technically strong laboratory professional with a background in chemistry, biology, engineering, analytical sciences, or a related field who also brings hands-on leadership experience. The R&D Supervisor will lead laboratory personnel and operations while supporting product development, design verification, method development, regulatory activities, and broader R&D initiatives.
Contract Pay Rate: Up to $51.50/hour (Contract to Perm Opportunity)
Applicants must be authorized to work in the U.S. without visa sponsorship now or in the future.
Key Responsibilities
- Lead, coach, mentor, and develop laboratory personnel while fostering a culture of quality and continuous improvement.
- Manage daily laboratory operations, testing priorities, resource allocation, and project deliverables.
- Coordinate laboratory testing, method development, qualification, validation, and troubleshooting activities.
- Establish project priorities and allocate resources based on business and R&D needs.
- Maintain and expand laboratory capabilities, infrastructure, equipment, and resource planning.
- Support capital equipment planning and laboratory investment strategies.
- Drive continuous improvement initiatives focused on laboratory efficiency, quality, productivity, and customer support.
- Develop and monitor laboratory metrics, project status, workload, and resource capacity.
- Communicate laboratory performance, risks, priorities, and project progress to management and key stakeholders.
- Partner cross-functionally with R&D, Design Assurance, Regulatory Affairs, Process Development, Manufacturing, Clinical, and Quality .
- Support product development, design verification testing, regulatory submissions, and other R&D programs .
- Ensure laboratory activities are performed in compliance with applicable quality systems, procedures, and regulatory requirements.
Technical Qualifications
- Strong understanding of laboratory operations within a regulated environment.
- Experience with test method development, qualification, validation, and troubleshooting .
- Knowledge of design verification and product development processes .
- Experience with statistical analysis and data interpretation.
- Familiarity with DOE, Minitab, data trending, and statistical methodologies .
- Strong project management, planning, prioritization, and organizational skills.
- Ability to analyze technical data and make sound recommendations.
Leadership Qualifications
- Demonstrated experience leading technical or laboratory teams.
- Ability to manage changing priorities and evolving business needs.
- Experience assigning resources, setting direction, and supporting multiple projects simultaneously.
- Strong coaching, mentoring, and employee-development skills.
- Proven ability to drive results through cross-functional collaboration.
- Strong communication and stakeholder-management skills.
Quality Responsibilities
- Maintain a strong commitment to patient safety and product quality .
- Ensure laboratory activities comply with applicable quality policies, procedures, and regulatory requirements.
- Maintain appropriate resources to support Quality System compliance.
- Promote a culture of quality, accountability, and continuous improvement.
Education & Experience
- Bachelor’s degree in Engineering, Chemistry, Biology, Science, or a related technical discipline .
- Minimum 4 years of experience in R&D, laboratory operations, analytical testing, method development, quality, or a related technical function within a regulated environment.
- Minimum 2 years of leadership experience , including direct people leadership, project leadership, or technical team leadership.
- Previous experience in a regulated industry , with medical device experience strongly preferred.
- Strong interpersonal, written communication, organizational, and leadership skills.
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