Engineer Lab Support

Work Schedule

Environmental Conditions

Job Description

This is a fully onsite role based at our GMP Laboratory in Middleton WI. We welcome applicants from all locations within the U.S. 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 without sponsorship.

• Must be able to pass a comprehensive background check which includes 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.

The Lab Support Engineer provides system analysis of new laboratory instrumentation as well as maintenance of existing instrumentation. Assists in the validation and qualification of laboratory instrumentation. Troubleshoots and repairs existing laboratory equipment and interacts with vendors and provides repair and maintenance of analytical instrumentation. The role involves supporting laboratory personnel in meeting specific sponsor timelines regarding analytical results.

What Youll Do:
Performs unit system test (i.e. IQ/OQ/PQ Calibration) and as needed
validation testing.
Prepares detailed system specifications based on user requirements for
instrumentation for the purpose of coordinating demonstration units with
vendors.
Develops/supervises instrumentation validation protocols for introduction into
mainstream analysis.
Prepares system documentation including requirements document
specification document test plans user manuals and SOPs for
instrumentation.
Oversees installment of new instrumentation. Trains staff and coordinates
deployment to operational areas. Troubleshoots and trains oncoming staff in
the troubleshooting of existing instrumentation.
Oversees/supervises junior level staff responsible for the same tasks.
Discovers and implements ways to increase instrument performance and
productivity.
Evaluates lab support records for compliance with SOPs reviews for
completeness and accuracy and reports findings.

Education & Experience Requirements:
Bachelors degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 8 years).

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:
Working knowledge and understanding of laboratory equipment and foundations of troubleshooting
Knowledge of mass spectrometry liquid chromatography relational databases and other analytical instrumentation operation
Working knowledge with systems in use at PPD or within the CRO/Pharmaceutical industry
Client focused approach with strong interpersonal skills
Strong analytical and problem solving skills
Ability to communicate effective with vendors clients and all levels of staff
Attention to detail and ability to multi-task
Ability to train others
Ability to work in a collaborative team environment.

Working Conditions and Environment:
Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
Occasional drives to site locations occasional domestic travel.
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.
Frequent 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 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 to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
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.