Principal Scientist, Purification
Company: Evote
Location: Seattle
Posted on: April 1, 2025
Job Description:
Just - Evotec Biologics' Purification Process Development group
is seeking an enthusiastic and hardworking team member who is
passionate about expanding worldwide access to biotherapeutics
through the advancement of continuous bioprocessing technology.
This person will join a fast-paced, collaborative, and
multidisciplinary team to support purification process development
at the bench and pilot scale for the advancement of low-cost
biotherapeutics manufacturing. Process design at Just-Evotec means
exposure to innovative technologies like high throughput automated
robotic screening and continuous processing technologies for a
first-of-its-kind flexible and reconfigurable end-to-end continuous
manufacturing facility.Key Responsibilities
- Leading a diverse team of scientists involved in purification
process development, characterization, and validation, including
technology transfer to cGMP manufacturing for hybrid and continuous
processes.
- Serving as an internal technical resource for cGMP
manufacturing and process design as well as a subject matter expert
for external clients and partners.
- Collaborating across the organization to accelerate clinical
development timelines and reduce costs.
- Effectively communicating scientific information and
experimental results to various stakeholders, both internal and
external.
- Authoring SOPs, reports, and slides to summarize and interpret
experimental data.
- Conducting risk assessment and authoring protocols for
late-phase process robustness and process characterization.
- Designing, executing, and analyzing statistically designed
experiments (DOE) for commercialization of late-phase
programs.
- Collaborating with vendors and manufacturers to develop, order,
and troubleshoot equipment prototypes.
- Mentoring, training, and supervising staff and interns.
- Driving technology development for process intensification and
continuous manufacturing to reduce costs and footprint.Education
and Experience
- BS/MS in Engineering, Biochemistry, Biology, or related field
with 12+ years of experience or Ph.D. in Engineering, Biochemistry,
Biology, or related field with 8+ years of experience.
- Expertise in purification technology and process development,
transfer to cGMP manufacturing plants, and authoring CMC sections
of regulatory filings.
- Experience with commercial process development, process
characterization, and validation.
- Expertise in design of experiments (DOE) and statistical
analysis with relevant statistical software.
- Experience in training, mentoring, and supervising team members
as well as leading development teams for external client projects
and collaborations and internal technology development
initiatives.
- Experience with high throughput process development systems is
a plus.Essential
- Proficiency in data analysis using tools such as JMP, R, or
Python.
- General understanding of cell biology, fluid dynamics,
mechanistic modeling, and protein chemistry, as well as knowledge
in other functional areas (upstream and analytical sciences).
- Experience working in a cGMP or clean room setting (GMP
knowledge is helpful).
- Strong written and verbal communication skills, including
client and multi-site communication.
- Familiarity with common software packages (e.g., Microsoft
Office).
- A curious, creative, and proactive mindset, with a strong
ability to work both independently and as part of a team to advance
scientific processes and technology.Additional Benefits, What We
Offer You In ReturnWe offer a competitive salary and a fantastic
benefits package and annual bonuses, plus, expenses covered where
travelling is required.The base pay range for this position at
commencement of employment is expected to be $140,000-$170,000;
Base salary offered may vary depending on individual's skills,
experience and competitive market value. Additional total rewards
include 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,
flexible work, generous paid time off and paid holiday, wellness
and transportation benefits.Evotec (US) Inc. is an Equal
Opportunity Employer. All qualified applicants will receive
consideration for employment without regard to race, gender, age,
disability, genetic information, gender expression, gender
identity, national origin, religion, sexual orientation, or veteran
status.
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Keywords: Evote, Seattle , Principal Scientist, Purification, Other , Seattle, Washington
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