Senior Scientist Bioassay - Site Based, Redmond, WA
EvotecRedmond, Washington, United States
Posted March 25, 2026
92400 - 125650 USD
Full Time
About the Company
Evotec is a biotechnology company that is committed to advancing drug discovery and development. Through flexible business models, we collaborate with pharmaceutical companies, biotechs, foundations, and government agencies on a substantial scale. We believe that by working together, we can make a difference in the lives of patients. Our Pipeline Co-Creation model represents our adaptable, multi-modality, fully integrated end-to-end approach to drive collaborations and services across all phases of drug discovery and development – from discovery of novel targets to achieving Proof of Concept in the clinic and into commercial manufacturing. We aspire to contribute data-driven disease understanding and early disease relevance in humans to bring the probability of success up. We select the right modality, which is then propelled forward on our platforms by our passionate people striving for the fastest and most effective ways towards patient impact. This is enabled by convergence of human ingenuity with data and AI. We also offer specific solutions, products, and CRO/CDMO-like services, always in support of the Biopharma R&D innovator. Our more than 4,000 scientists work closely with numerous partners concurrently, delivering fully integrated research and development portfolios or individual projects with the highest quality standards and efficiency, coupled with great science, passion, engagement, and communication.
Job Description
Just Evotec Biologics is seeking a Senior Scientist Bioassay to join their team. The ideal candidate will have a BS in Chemistry, Biochemistry, or related field with a minimum of five years of Quality Control experience in GMP biopharmaceutical or biotechnology industry. The role will involve performing routine/non-routine QC testing using Bioassay methods, ensuring timely and accurate completion of GMP documentation, and collaborating with Analytical Development to generate and approve protocols, reports, and other technical documents.
Requirements
- BS in Chemistry, Biochemistry, or related field
- Minimum of five years of Quality Control experience in GMP biopharmaceutical or biotechnology industry
- Extensive laboratory experience with either Bioassay (ELISA; PCR; HCP; ProA; cell-based potency) techniques
- Experience with capillary electrophoresis or chromatography data systems
- Knowledge of GMP regulations and experience with regulatory compliance inspections
- Ability to adapt, work in a fast-paced environment, manage multiple projects and priorities at the same time
- Excellent oral/written and interpersonal communication skills
- Knowledge of Microsoft Office Suite (Excel, Word, PowerPoint)
- Ability to work independently and with others to accomplish goals and priorities
- Effective time management skills, demonstrate initiative, resourcefulness and flexibility to work independently and as part of a team
Benefits
- Discretionary annual bonus
- Comprehensive benefits to include Medical, Dental and Vision
- Short-term and long-term disability
- Company paid basic life insurance
- 401k company match
- Generous paid time off
- Paid holiday
- Wellness and transportation benefits
