Senior Scientist Site based, Redmond, WA
Senior Scientist Site based, Redmond, WA
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Job Description
Job Title: QC Analytical Senior Scientist
Location: Redmond WA visiting as required Seattle.
Shifts: Monday to Friday days. 8:00 till 17:00
About Us: this is who we are
At Just Evotec Biologics we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team we thrive on challenging the status quo learning from each other and pushing the boundaries of whats possible. Were on a mission to create a place where curiosity isnt just encouragedits celebrated.
Are you someone who asks questions seeks answers and isnt afraid to go deeper #BeCureious with us and see where your curiosity can take you!
The Role: / your challenge in our journey
Were looking for a passionate and curious senior scientist to join our team. If youre excited by new challenges solving complex problems and learning every step of the way you might just be the perfect this role youll have the opportunity to drive impactful projects collaborate with bright minds and explore uncharted territories.
As a senior scientist at Just Evotec Biologics youll have the freedom to ask the hard questions think outside the box and find creative solutions that push us forward. Its a role where your curiosity will fuel both your personal growth and the success of the team.
This role provides the QC analysis of raw materials in-process drug substance and drug product samples in support of our GMP manufacturing operations at the Seattle and Redmond WA GMP facilities. These efforts support GMP manufacturing activities for biotherapeutic products.
What Youll Do:
Dive deep into investigations method validations and analytical separation methods always looking for ways to improve and innovate.
Collaborate with cross-functional teams to explore new possibilities and solutions.
Bring fresh perspectives to routine testing qualification and validations that challenge the status quo.
Regularly share your findings ideas and solutions in both team settings and presentations.
Keep up with the latest trends and developments in biotechnology and pharmaceuticals and use your knowledge to inspire and lead.
Ensure that curiosity-driven questions and exploration lead to measurable impactful results.
Perform routine/non-routine QC testing using chromatographic and physiochemical methods.
Ensure timely and accurate completion of GMP documentation.
Collaborate with Analytical Development to generate and approve protocols reports and other technical documents required for the qualification and transfer of analytical methods.
Conduct laboratory investigations deviations OOS change controls and CAPAs.
Support equipment qualification (IQ OQ PQ).
Support QC management in the timely review of data.
Develop revise and review SOPs methods and associated documents.
Support all operations of the QC labs including the ordering supplies maintaining laboratory equipment and lab spaces and logbook reviews.
Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on analytical related matters.
Participate in daily and weekly operation meetings.
Provide on-the-floor mentorship training and technical leadership for less experienced staff as an individual contributor.
Who You Are:
A curious problem-solver with a passion for learning and growing in a dynamic environment.
Someone who is not satisfied with just good enough and is always looking to improve adapt and innovate.
A natural collaborator who loves sharing ideas and learning from others.
Comfortable with ambiguity and thrives in environments where curiosity and experimentation are encouraged.
Excellent communicator both verbally and in writing able to share complex ideas in a simple relatable way.
BS in Chemistry Biochemistry or related field with a minimum of five years of Quality Control experience in GMP biopharmaceutical or biotechnology industry.
Extensive laboratory experience with either HPLC / UPLC chromatography systems or capillary electrophoresis 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.
Ability to work independently and with others to accomplish goals and priorities.
Must possess effective time management skills demonstrate initiative resourcefulness and flexibility to work independently and as part of a team.
Why Join Us:
Growth Opportunities: Were a company that believes in continuous learning and development. Whether its professional courses mentorship or new projects well help you grow.
Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based Redmond WA visiting Seattle WA as required.
Inclusive Culture: Were committed to building a diverse and inclusive environment where everyones voice is valued and curiosity is encouraged.
Innovative Projects: Youll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.
A Place for Big Ideas: We dont just talk about thinking outside the boxwe throw the box away. If youve got ideas we want to hear them.
Are You Still Curious
If youve read this far then chances are youve got a curious mindjust like us. So what are you waiting for Take the leap and apply today. We cant wait to see where your curiosity leads youand how it will shape the future of Just Evotec Biologics.
Let your curiosity guide your career#BeCurious and explore the endless possibilities at Just Evotec Biologics!
The base pay range for this position at commencement of employment is expected to be $92400 to $126500; Base salary offered may vary depending on the individuals 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.
Required Experience:
Senior IC
Employment Type
Full-Time
