Job Description
Job Summary:
- Responsible for analytical testing to support pharmaceutical process development.
- You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects.
Duties and Responsibilities:
- Perform laboratory testing to assess the potency, performance, and safety of new pharmaceutical products.
- Interpret client documents and literature to strategize approaches for successful method development, qualification, and/or method transfer activities.
- Responsible for performing in-depth analysis of analytical data and collaborate with the analytical team for method lifecycle review.
- Communicate findings and discuss relevance of your data to a multi-discipline team consisting of upstream and downstream process development scientists, quality control, quality assurance, process engineers and our customers.
Education & Experience:
- Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field.
- B.S. or M.S with 2 – 3yrs experience or Ph.D. with 0-1 yr work experience.
- Experience working in a GxP environment and ALCOA+ documentation practices.
- Experience using analytical laboratory techniques to efficiently and accurately prepare sample and standard solutions for analysis.
Knowledge, Skills, Abilities:
- High attention to detail.
- Strong desire to learning new skills.
- Knowledge and Technical expertise in performing analytical assessment on pharmaceutical products and raw materials including but not limited to high-performance liquid chromatography (HPLC), Gas Chromatography (GC), and Mass Spectrometry (MS).
- Ability to work independently with excellent communication, planning, and prioritization skills.