Entry Level Scientist - Cell Gene Therapy
About The Position
The Scientist I performs high-quality sample testing for pharmaceutical clients using innovative technologies. Sample preparation and analysis support the development and delivery of life-changing therapies. Under general supervision, the role conducts complex analysis and routine sample preparation and analysis to quantitatively measure pharmaceutical and biopharmaceutical compounds in different formulations and biological matrices for stability and analytical testing. The position also involves training on analytical instrumentation, standard operating procedures (SOPs), and regulatory guidelines, as well as reviewing and compiling results and comparing data against acceptance criteria, methodologies, protocols, and product specifications. This is a fully onsite role at a GMP laboratory in Middleton, Wisconsin. The standard schedule is Monday through Friday. Laboratory and office work may require personal protective equipment, and may involve exposure to potentially hazardous elements, including infectious agents. Applicants must be legally authorized to work in the United States without sponsorship and must pass a comprehensive background check, including a drug screen. Relocation assistance is not provided.
Requirements
- Bachelor's degree, preferably in life sciences, or equivalent and 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 work collaboratively with a team or independently with supervision.
- Ability to follow detailed written and verbal instructions and complete assignments within expected time frames.
- Ability to communicate, receive, and understand information and ideas with diverse groups of people.
- Ability to work upright and stationary and/or standing for typical working hours.
- Ability to lift and move objects weighing up to 25 pounds.
- Ability to work in non-traditional work environments and use and learn standard office equipment and technology.
- Ability to perform successfully under pressure while prioritizing and handling multiple projects or activities.
- Legally authorized to work in the United States without sponsorship.
- Ability to pass a comprehensive background check, including a drug screen.
Responsibilities
- Perform routine sample preparation and analysis to quantitatively measure pharmaceutical and biopharmaceutical compounds in various formulations and biological matrices for stability and analytical testing.
- Conduct complex analysis under general supervision.
- Train in 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.
- Manage time and assignments effectively, including prioritizing multiple projects or activities.
Benefits
- Accessibility services and accommodations are available to job seekers with disabilities during the application process.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
