Scientist II - ICP Mass Spec - M-F 2nd Shift

Thermo Fisher Scientific•Middleton, WI

6d•Onsite

About The Position

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, you’ll 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. Division Specific Information As a Scientist you will work in a multi-functional environment supporting drug development and will collaborate in cross-functional teams. You will accomplish our mission through innovation and partnership, creative problem-solving, and use of state-of-the-art technology.

Requirements

Bachelor's degree in lab sciences such as chemistry, biochemistry, or similar
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
Knowledge of routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory guidelines.
Knowledge of applicable regulatory authority, compendia and ICH guidelines.
Demonstrates excellent manual dexterity skills, allowing for precise and accurate work.
Exhibits strong written and oral communication skills, facilitating effective communication within the team and with stakeholders.
Displays exceptional time management and project management skills, ensuring efficient completion of tasks.
Proven problem-solving and troubleshooting abilities, enabling the identification and resolution of issues.
Capable of cross-training on sample preparation techniques with another laboratory group, enhancing versatility and collaboration.
Thrives in a collaborative work environment, actively contributing to a cohesive and productive team to demonstrate behaviors which align to the 4i Values of Thermo Fisher.

Responsibilities

Trains on routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.
Performs a variety of routine to complex sample preparation and analysis procedures with minimal supervision/guidance to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.
Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.
Independently troubleshoots equipment & instruments.
Mentors' others in troubleshooting when applicable.
Reviews and complies results from assignments and makes initial determination on acceptability per SOP acceptance criteria.
Performs work assignments accurately, and in a timely and safe manner.
Independently manages QC responsibilities.
Communicates' project status to project leader and helps to identify gaps and anticipates roadblocks in project team workflow.
Completes QA facing tasks with minimal supervisor/QA input.
Authors low complexity quality records and participates in the OOS/OOT/Atypical investigation process.