Senior Scientist I, Potency and Impurities
About The Position
Just-Evotec is seeking a motivated and creative Senior Scientist I who is excited about expanding global access to biotherapeutics. The candidate will join a fast-paced, collaborative, and multidisciplinary team responsible for analytical testing. The successful candidate will develop and perform method qualification for potency assays, support early-phase CMC programs, and drive analytical strategy. The ideal candidate is skilled in experimental design, data analysis, and communication skills, thrives in both independent and team-based environments and is excited by advancing new technologies. This role also includes opportunities to lead cross-functional initiatives and mentor junior scientists. As a Senior Scientist I at Just-Evotec, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.
Requirements
- PhD with 3+ years of relevant industry experience, or BS with 10+ years of experience, with a degree in Biochemistry, Biology, Bioengineering, or related field
- Immunoassay method development and qualification experience
- GMP Testing experience
- Comprehensive knowledge of ICH/USP guidelines on analytical and potency methods
- Excellent communication skills; the ability to work cross functionally in a fast-paced CDMO environment
- Strong organizational skills with the ability to manage multiple priorities, meet deadlines, and maintain high quality standards
Nice To Haves
- Experience utilizing industry-standard applications (e.g., SoftMax Pro, JMP, Microsoft Office, ELN)
- Development of biolayer interferometry (BLI) or surface plasmon resonance (SPR) methods
- Knowledge of impurity methods for biotherapeutics
- Experience with compendial method testing
Responsibilities
- Serve as subject matter expert for potency and immunoassays for early stage biotherapeutics across multiple platforms
- Perform method development, qualification, and routine sample testing
- Apply working knowledge of ICH, FDA, EMA, and USP guidelines relevant to analytical testing
- Participate in process development teams; may serve as analytical team lead and interface with internal teams and external clients
- Author and review technical documents including methods, qualification and development reports, and SOPs
- Present data to internal teams, clients, and at industry conferences
- Lead cross-functional teams and initiatives and junior team members
- Ensure proper maintenance and calibration of lab equipment; oversee reagent and consumable management
- Contribute to continuous improvement initiatives to enhance throughput, robustness, and compliance
Benefits
- Medical
- Dental
- Vision
- short-term and long-term disability
- company paid basic life insurance
- 401k company match
- flexible work
- generous paid time off
- paid holiday
- wellness and transportation benefits
- discretionary annual bonus
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What This Job Offers
Job Type
Full-time
Career Level
Senior
