Associate Scientist, Seperations

Thermo Fisher Scientific • Wilmington, DE

1d • Onsite

About The Position

Join us as an Associate Scientist I This is a fully onsite role based at our customer’s site in Wilmington,DE. We welcome applicants from all locations within the US. 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. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. The Associate scientist will perform a variety of routine to 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.

Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification and 1+ years of experience OR MS degree in relevant scientific degree
• 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 of applicable regulatory authority, compendia and ICH guidelines
• Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use
• Ability to utilize Microsoft Excel and Word to perform tasks
• Ability to independently optimize analytical methods
• Good written and oral communication skills
• Time management and project management skills
• Problem solving and troubleshooting abilities
• Ability to work in a collaborative work environment with a team

Nice To Haves

• Experience with HPLC, UPLC, Capillary Electrophoresis, cIEF is a plus.
• Wet chemistry, pipetting, liquid chromatography is a plus.

Responsibilities

• Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.
• Solves problem with assistance pertaining to sample handling and/or instrumentation problems.
• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and safety procedures and guidelines.
• 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 Laboratory Practices (GLP).
• Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to customers.
• Plan, perform, analyze, and document laboratory experiments in support of antibody development.
• Present/conclude data summaries.

What This Job Offers

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