Senior Analytical Scientist
About The Position
In this role you will be involved with problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing. Serve as a subject matter expert in analytical development, perform troubleshooting / provide efficient and innovative solutions, and support transfer of analytical methods to GMP QC labs. Utilize customer-facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposals. Serve as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensures process and methods are in place for efficient GMP start. Lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities.
Requirements
- Bachelor’s Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 6+ years of research experience.
- Master’s Degree in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 2+ years of research experience.
- PhD in in Chemistry, Biochemistry, Biomedical Engineering, Chemical Engineering or other Life Science or Engineering discipline and 1+ years of research experience.
Nice To Haves
- Experience with protein characterization via ELISA, SPR, Isoelectric Focusing, CE-based methods, UV-Vis, and/or chromatography (HPLC/GC/IC/UPLC/SEC/HILIC).
- Experience with advanced laboratory techniques; theory and practice to enable the development of novel approaches to solve complex process and analytical problems on fast-paced projects with changing priorities.
- Knowledge of small molecule or bio-therapeutics drug development process.
- Experience with antibody-drug conjugation.
- Knowledge in Biochemistry or Organic Chemistry.
- Experience in automation in an analytical setting and instrument maintenance and troubleshooting.
- Knowledge of Microsoft Word, Excel, and PowerPoint.
- Experience with advanced data acquisition and/or statistical software systems.
- Ability to coordinate information exchange and manage data generated by contract testing labs.
Responsibilities
- Problem solving
- Working within project timelines
- Contributing to documentation for method qualification and transfer into GMP manufacturing
- Serve as a subject matter expert in analytical development
- Perform troubleshooting / provide efficient and innovative solutions
- Support transfer of analytical methods to GMP QC labs
- Utilize customer-facing skills
- Document experimental results
- Communicate results to all stakeholders
- Author method development and qualification documents
- Contribute to information for customer proposals
- Serve as a project lead and ensure project deliverables are on quality and on time
- Develop multiple technical approach plans as needed to solve problems and mitigate risk
- Ensures process and methods are in place for efficient GMP start
- Lead project teams
- Influence exemplary work in other team members
- Lead process improvement initiatives
- Scout for new technologies / emerging trends
- Proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities
Benefits
- health insurance
- paid time off (PTO)
- retirement contributions
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
