Supervisor, Cell Lab (Tuesday - Saturday)

Thermo Fisher Scientific•Middleton, WI

3d•Onsite

About The Position

This is a fully onsite role based at our GMP Laboratory in Middleton, WI. Thermo Fisher Scientific's mission is to enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. As a Lab Supervisor, you will coordinate staffing and resources, support day-to-day workflows, and assist in preparation and implementation of company policies, quality systems and training programs. This role ensures that projects are completed in a timely manner so that company revenues are met, and clients are satisfied with the quality and turnaround of work being performed. The Lab Supervisor also ensures that staff continue to be developed to keep pace with department goals and growth.

Requirements

Bachelor's degree or equivalent preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years) or equivalent and relevant combination of education, training, & experience.
1+ year demonstrated leadership qualities
Demonstrated proficiency of good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging deadlines.
Proven leadership skills
Ability to train and mentor junior staff
Demonstrated ability to be project solution driven
Good written and oral communication skills as well as presentation skills
Can independently perform root cause analysis
Technical writing skills; ability to write quality documents (SOPs, investigation forms, etc.)
Demonstrated knowledge of QA metrics of program base; ability to write and recommend changes to PPD SOPs
Project and time management skills
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Nice To Haves

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Responsibilities

Supervises the daily activities of staff, including interviewing, selection, hiring, professional development, performance management, and reviews and approves time records, requests for leave, and overtime.
Manages daily workflow, allocates resources, and tracks performance metrics.
Identifies and recommends process improvements and efficiency gains to optimize processes.
Monitors and ensures compliance with quality standards, investigates and resolves complex problems through root cause analysis, and implements corrective actions.
Responds to facility audit findings.
Assists management in their responsibilities.
Assists in preparation and implementation of PPD/client SOPs and company operational policies.
Ensures adherence to SOPs, safety standards and company policies.