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Astrix Technology Bioanalysis Scientist III in Fulton, Missouri

Bioanalysis Scientist III

Science & Research

Fulton , MO, US

Pay Rate Low: 32.00 | Pay Rate High: 34.00

  • Added - 10/09/2024

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Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Scientist III to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference!

Schedule : M-F 1 st

Type : Contract to hire

Pay : $32-$34/hr

The Scientist III (Bioanalysis) is responsible for initiating, developing, and performing assays leading to the quantitative determination of drug and metabolites in biological matrices (e.g., plasma, tissue, environmental etc.) using LCMS and/or HPLC instruments in accordance with local and global regulatory requirements.

Requirements:

  • Master’s degree from an accredited institution with one-plus (1+) years of experience in a related scientific discipline (Chemistry, Analytical chemistry, Biochemistry preferred)

  • OR Bachelor’s degree from an accredited institution with seven-plus (7+) years of experience in related scientific discipline.

  • Capable of performing quantitative analysis using HPLC, LC/MS-MS instruments.

  • Prior pharmaceutical industry R&D experience.

  • Knowledge of GLP and a good understanding of FDA and EMEA regulatory requirements for drug product registration.

Responsibilities:

  • Analysis for pharmacokinetics, metabolism, human food safety, efficacy, and target animal safety studies to support the development of new products and the maintenance of existing products.

  • Independently operates and troubleshoots lab equipment’s (e.g., LCMS/HPLC) and is independently responsible for maintaining in a validated state.

  • Performing method demonstration for regulatory agency and participating in method trials.

  • Maintains proper records in accordance with SOPs and policies. Ability to strictly follow SOPs.

  • Records, evaluates, interprets, and reviews technical data with limited supervision in compliance with regulatory requirements and prepares data for inclusion in project reports.

  • Proposes new experiments/technologies based on science as well as overall understanding of drug discovery/development process.

  • Ensures a safe working environment in the laboratory and office according to HSE policies.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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