Scientist II - Small Molecule - Middleton, WI

Thermo Fisher Scientific • Middleton, WI

354d

About The Position

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!

Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
• Demonstrated knowledge of HPLC or LCMS.
• Proficient in Microsoft Excel and Word.
• Proven track record to interpret data by performing trend analysis.
• Proven track record in technical writing skills.
• Ability to independently optimize analytical methods.
• Proven problem solving and troubleshooting abilities.
• Good written and oral communication skills.
• Time management and project management skills.
• Ability to work in a collaborative work environment with a team.

Responsibilities

• Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence.
• Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices.
• Follows validated or experimental analytical procedures with periodic direct supervision.
• Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.
• Enters data into databases and reports.
• Performs self-review for own data prior to QC submission.
• Works with multiple functional groups to meet business needs.
• Plans and organizes work with periodic supervision.
• Sets up and maintains analytical instrumentation.
• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
• Ensures QA findings are addressed appropriately.
• Aids and trains other team members.
• Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems.
• Communicates project status to project leader.
• Performs work assignments accurately, and in a timely and safe manner.
• Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
• Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.

What This Job Offers

• Industry: Computer and Electronic Product Manufacturing
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees