Evotec
Validation Engineer II - Redmond/Seattle, WA, Site Based
Evotec, Redmond, Washington, United States, 98052
Overview
Job Title:
Validation Engineer II
Location:
Redmond, Seattle, WA
Shifts:
Monday to Friday, 8:00am till 5:00pm
Some flexibility as may be required, as business needs to come in over the weekend.
About Us this is who we are
At
Just
Evotec Biologic , 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 what’s possible. We\'re on a mission to create a place where curiosity isn’t just encouraged—it’s celebrated.
Are you someone who asks questions, seeks answers, and isn\'t afraid to go deeper?
#BeCureious
with us and see where your curiosity can take you!
The Role The Role: / your challenge, …in our journey
We’re looking for a passionate and curious Validation Engineer II to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.
As a Validation Engineer II at
Just
Evotec Biologic , 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.
The primary focus of this job is to support manufacturing and laboratory equipment, systems, facilities, and utilities commissioning, qualification and validation activities required in early phase manufacturing to late-stage programs into PPQ/ commercial biologics manufacturing. These responsibilities span all phases of the lifecycle from system implementation and qualification to cleaning and shipping validation. This role will also work cross functionally and collaborate with other teams on validation projects.
What You’ll Do
Execute FUSE commissioning and validation activities for early stage clinical manufacturing, late-stage molecule/ commercial manufacturing and/or PPQ campaign support.
Generate and review technical documentation including validation lifecycle documents, validation protocols and associated reports related to the equipment validation lifecycle.
In collaboration with cross functional teams, develop Validation Master Plans, provide process knowledge to support the validation execution and risk assessments.
Lead the development and implementation of templates and validation workflows.
Support the generation of governance policies and related SOPs for commissioning of FUSE.
Support validation deviation resolution including troubleshooting and root cause analysis
Support the periodic review of qualified/validated FUSE across JUST WA sites.
Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings
Who You Are
Bachelor’s degree in engineering science or related program with minimum 2 years relevant experience.
Proven experience in executing commissioning and validation activities of FUSE.
Understanding of GMP concepts and Quality systems necessary to execute validation activities.
Understanding of industry standards and best practices for a science and risk-based approach to qualification of systems, equipment, utilities, and/or facilities
Knowledge of process equipment, utilities, operations, and engineering principles
Experience in quality risk management
Must possess problem-solving and critical thinking skills
Good interpersonal, team, and collaborative skills
Motivated, self-starter with strong mechanical aptitude
Ability to work both independently and collaboratively across multiple disciplines in a fast-paced and dynamic environment
Proven knowledge of cGMP requirements and experience writing manufacturing technical documents
Experience leading technical projects and managing timelines with external collaborators and vendors
Candidate must possess a strong focus on quality and attention to detail as well as effective task/ time management organizational skills
Additional Preferred Qualifications
Understanding of biologics manufacturing process and process automation (e.g. DeltaV)
Experience with single-use technologies and systems
Previous work experience with Complex Equipment, Distributed Control System (DCS), Building Automation Systems (BAS), PLC, SCADA, PI, and MES will be a plus
Working knowledge of utilities and facilities, computerized systems, analytical equipment, process validation and clean validation methodologies.
Significant contributor to multi-disciplinary teams at the functional level
Authority inspection or audit support involvement.
Why Join Us
Growth Opportunities : We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
Flexible Work Environment : We offer flexible work options to help you balance your professional and personal life. Site based role.
Inclusive Culture : We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
Innovative Projects : You’ll 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 don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
Are You Still Curious?
If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of
Just
Evotec Biologic .
Let your curiosity guide your career— #BeCurious
and explore the endless possibilities at
Just
Evotec Biologic !
The base pay range for this position at commencement of employment is expected to be $79,800 to $109,250; Base salary offered may vary depending on the 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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Validation Engineer II
Location:
Redmond, Seattle, WA
Shifts:
Monday to Friday, 8:00am till 5:00pm
Some flexibility as may be required, as business needs to come in over the weekend.
About Us this is who we are
At
Just
Evotec Biologic , 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 what’s possible. We\'re on a mission to create a place where curiosity isn’t just encouraged—it’s celebrated.
Are you someone who asks questions, seeks answers, and isn\'t afraid to go deeper?
#BeCureious
with us and see where your curiosity can take you!
The Role The Role: / your challenge, …in our journey
We’re looking for a passionate and curious Validation Engineer II to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.
As a Validation Engineer II at
Just
Evotec Biologic , 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.
The primary focus of this job is to support manufacturing and laboratory equipment, systems, facilities, and utilities commissioning, qualification and validation activities required in early phase manufacturing to late-stage programs into PPQ/ commercial biologics manufacturing. These responsibilities span all phases of the lifecycle from system implementation and qualification to cleaning and shipping validation. This role will also work cross functionally and collaborate with other teams on validation projects.
What You’ll Do
Execute FUSE commissioning and validation activities for early stage clinical manufacturing, late-stage molecule/ commercial manufacturing and/or PPQ campaign support.
Generate and review technical documentation including validation lifecycle documents, validation protocols and associated reports related to the equipment validation lifecycle.
In collaboration with cross functional teams, develop Validation Master Plans, provide process knowledge to support the validation execution and risk assessments.
Lead the development and implementation of templates and validation workflows.
Support the generation of governance policies and related SOPs for commissioning of FUSE.
Support validation deviation resolution including troubleshooting and root cause analysis
Support the periodic review of qualified/validated FUSE across JUST WA sites.
Support inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findings
Who You Are
Bachelor’s degree in engineering science or related program with minimum 2 years relevant experience.
Proven experience in executing commissioning and validation activities of FUSE.
Understanding of GMP concepts and Quality systems necessary to execute validation activities.
Understanding of industry standards and best practices for a science and risk-based approach to qualification of systems, equipment, utilities, and/or facilities
Knowledge of process equipment, utilities, operations, and engineering principles
Experience in quality risk management
Must possess problem-solving and critical thinking skills
Good interpersonal, team, and collaborative skills
Motivated, self-starter with strong mechanical aptitude
Ability to work both independently and collaboratively across multiple disciplines in a fast-paced and dynamic environment
Proven knowledge of cGMP requirements and experience writing manufacturing technical documents
Experience leading technical projects and managing timelines with external collaborators and vendors
Candidate must possess a strong focus on quality and attention to detail as well as effective task/ time management organizational skills
Additional Preferred Qualifications
Understanding of biologics manufacturing process and process automation (e.g. DeltaV)
Experience with single-use technologies and systems
Previous work experience with Complex Equipment, Distributed Control System (DCS), Building Automation Systems (BAS), PLC, SCADA, PI, and MES will be a plus
Working knowledge of utilities and facilities, computerized systems, analytical equipment, process validation and clean validation methodologies.
Significant contributor to multi-disciplinary teams at the functional level
Authority inspection or audit support involvement.
Why Join Us
Growth Opportunities : We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.
Flexible Work Environment : We offer flexible work options to help you balance your professional and personal life. Site based role.
Inclusive Culture : We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
Innovative Projects : You’ll 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 don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.
Are You Still Curious?
If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of
Just
Evotec Biologic .
Let your curiosity guide your career— #BeCurious
and explore the endless possibilities at
Just
Evotec Biologic !
The base pay range for this position at commencement of employment is expected to be $79,800 to $109,250; Base salary offered may vary depending on the 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.
#J-18808-Ljbffr