Scientist I Cell Lab - Multiple Shifts Available

Thermo Fisher Scientific • Middleton, WI

9d • Onsite

About The Position

The Scientist I works onsite in Thermo Fisher Scientific’s GMP Laboratory in Middleton, Wisconsin, performing sample testing for pharmaceutical clients. Under general supervision, the role conducts routine sample preparation and analysis to quantitatively measure pharmaceutical and biopharmaceutical compounds in formulations and biological matrices for stability and analytical testing. The work contributes to bringing therapies to market by supporting accurate, high-quality laboratory results.

The position includes training in the routine operation, maintenance, and theory of analytical instrumentation, as well as applicable standard operating procedures and regulatory guidelines. The Scientist reviews and compiles results and compares data against acceptance criteria, methodologies, protocols, and product specifications. The role may involve cross-training with another laboratory group and working collaboratively or independently under supervision.

Requirements

• Bachelor’s degree, preferably in Life Sciences, or equivalent relevant formal academic or vocational qualification.
• Previous experience providing the knowledge, skills, and abilities to perform the job; comparable to 0–2 years or an equivalent combination of education, training, and experience.
• Knowledge of routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory guidelines.
• Knowledge of applicable regulatory authorities, compendia, and ICH guidelines.
• Excellent manual dexterity.
• Good written and oral communication skills.
• Time-management and project-management skills.
• Problem-solving and troubleshooting abilities.
• Ability to follow detailed written and verbal instructions.
• Ability to work collaboratively in a team environment or independently with supervision.
• Ability to work effectively under pressure and prioritize multiple projects or activities.
• Must be legally authorized to work in the United States without sponsorship.
• Must pass a comprehensive background check, including drug screening.

Responsibilities

• Perform routine sample preparation and analysis to quantitatively measure pharmaceutical and biopharmaceutical compounds in formulations and biological matrices.
• Conduct stability and analytical testing under general supervision.
• Train on the routine operation, maintenance, and theory of analytical instrumentation, SOPs, and regulatory guidelines.
• Review and compile results and compare data against SOP acceptance criteria, methodology, protocol, and product specifications.
• Cross-train on sample preparation techniques with another laboratory group.
• Complete assignments within expected time frames while managing multiple projects or activities.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level