Lab Support Supervisor Stability and Storage

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profile Job Location:

Middleton, ID - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office

Job Description

Position: Supervisor

Location: Middleton Wisconsin

Department: Lab Support Stability and Storage

This is a fully onsite role based at our GMP Laboratory in Middleton WI. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States withoutsponsorship.Must be able to pass a comprehensive background check whichincludes a drug screening.

At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling 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. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.

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.

Discover Impactful Work:

Provides line-level management coordination of resources and work schedules. Oversees daily operations and assists in preparation and implementation of company policies quality systems and training programs. Ensures that projects are completed in a timely manner so that company revenues are met and clients are satisfied with the quality and turnaround time of work being performed. Ensures that staff continues to be developed to keep pace with department goals and growth.

A Day in the Life:

  • 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

Keys to Success:

Education

  • Bachelors 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.

Experience

  • 1 year demonstrated leadership qualities preferred

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.

Knowledge Skills Abilities

  • Experience with preventative maintenance qualification calibration and operation of temperature/humidity chambers analytical instrumentation or related equipment preferred.

  • Knowledge of GMP or other regulatory experience preferred.

  • 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

Work Environment

  • Work is performed in an office and/or a laboratory and/or a clinical environment with exposure to electrical equipment.

  • Occasionally drives to site or client locations occasionally travels within the United States.

  • Exposure to biological fluids with potential exposure to infectious organisms. Rare exposure to skin and lung irritants radiation toxic materials and hazardous waste.

  • Personal protective equipment required such as protective eyewear garments and gloves.

  • Exposure to fluctuating and/or extreme temperatures on rare occasions.

  • Frequently stationary for 6-8 hours per day.

  • Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists.

  • Occasional mobility required.

  • Occasional crouching stooping bending and twisting of upper body and neck.

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

  • Ability to communicate moderately complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.

  • Frequently interacts with others relates sensitive information to diverse groups.

  • Ability to apply basic principles to solve conceptual issues.

  • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.

  • Regular and consistent attendance.

Benefits

We offer competitive remuneration annual incentive plan bonus healthcare and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation!

Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.

Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example this may include individuals requiring assistance because of hearing vision mobility or cognitive impairments. If you are a job seeker with a disability or assisting a person with a disability and require accessibility assistance or an accommodation to apply for one of our jobs please submit a request by telephone at 1-*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes such as not being able to get into the career website following up on an application or other non-disability related technical issues will not receive a response.


Required Experience:

Manager

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards OfficeJob DescriptionPosition: SupervisorLocation: Middleton WisconsinDepartment: Lab Support Stability and StorageThis is a fully onsite role based at our GMP Laboratory in Mi...
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Key Skills

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