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Ultimate Staffing Services
Associate Scientist - PS
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What they do
A Pharmacology Research Scientist performs scientific research with the aim of discovering new solutions or improving existing ones within the field of use and effects of drugs.
$126,238 / year median in California
+8% projected growth
Job Description
We are hiring for an Associate Scientist (Pharmaceutical Sciences) with 1-3 years of lab experience. You will have an opportunity to join a leading biopharmaceutical company based in Irvine, CA! •NOTE•: This position is fully onsite 5-days a week in Irvine, CA. Candidates MUST be local to Orange County, CA. We are looking for inspired individuals who are motivated to grow professionally, while building a best-in-class pharmaceutical company with a differentiated approach. Join us in advancing our mission to focus on unmet needs and apply proven science and new technology to revolutionize treatment for patients.
Author and review internal notebook entries documenting lab work in timely manner and treat data with a high level of integrity and ethics. Review internal and external technical documents and author technical memos, scientific presentations, and reports. Complete trainings assigned by the Quality department as part of being a GxP employee in a timely manner.
Overview:
Under supervision of the Manager and Sr Scientist of Pharmaceutical Sciences, the Associate Scientist will be involved in the development, designing, and performing and/or management of experiments to support products' development at various stages of their lifecycles. This individual will be involved in the formulation, preparation and characterization of experimental formulations, writing and reviewing of technical documents and reports, maintenance of lab instruments, and other general lab duties.Key responsibilities:
Help design and conduct formulation studies to support formulation and manufacturing process development with assistance and supervision of Sr Scientist, Pharmaceutical Sciences. Demonstrates strong laboratory practices, attention to detail, and the ability to generate accurate, reproducible, and well-documented experimental data.Author and review internal notebook entries documenting lab work in timely manner and treat data with a high level of integrity and ethics. Review internal and external technical documents and author technical memos, scientific presentations, and reports. Complete trainings assigned by the Quality department as part of being a GxP employee in a timely manner.