Validation Engineer III, Cleaning & Shipping

Validation Engineer III, Cleaning & ShippingLocation: Redmond, WAReports to: Director, ValidationAbout Us:At Just-Evotec, 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? #BeCurious with us and see where your curiosity can take you!The Role:We're looking for a passionate and curious Validation Engineer III 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.Just-Evotec is seeking a highly motivated Validation Engineer III that desires a significant opportunity to improve worldwide access to biotherapeutics. A few focus areas of this job include to strategize, implement and support cleaning, shipping and process validation activities required for late phase and commercial biologics manufacturing as part of a fast-paced and collaborative global validation team. Manufacturing and laboratory equipment, systems, facilities, and utilities commissioning, qualification and validation activities maybe supported as part of this role as required.What You'll Do:Lead the generation of key deliverables in a phase appropriate compliance manner as part of global CQV strategy for F&U, Equipment, QC/Analytical, Cleaning and ShippingDocument a strategy for validations programs including the generation of validation master plansLiaise with the equipment, operations, logistics, qc, tech transfer, process development teams and third-party contractors, as applicable, to define and identify and perform cycle development, qualification and validation activitiesAuthor validation documentation including, but not limited to, risk and gap assessments, cycle development protocols / reports / procedures, qualification/validation protocols and reports, and validation discrepancies.Lead validation discrepancy resolution including troubleshooting and root cause analysisSupport the development of the qualification and validation programs at Just including the transition from paper based to digital validation software to configure globally scalable end to end paperless solutions to manage the validation lifecycleDevelop and strategize compliant and novel ways to comply with regulatory requirementsSupport inspection readiness activities, Health Authority and Client audits, and support corrective actions based on audit findingsLead CQV activities across global expansion sitesWho You Are:Bachelor's degree in engineering science or related program with the following years in relevant experience: 7+ yearsExpert knowledge of shipping and cleaningUnderstanding of industry standards and best practices for a science and risk-based approach to qualification of systems and processesWorking knowledge of US FDA CFRs and European EMA, including ICH regulationsExperience with quality risk managementExperience authoring, reviewing, and approving validation documentationKnowledge of process equipment, utilities, operations, and engineering principlesMust possess a strong focus on quality and attention to detailMust possess problem-solving and critical thinking skillsMotivated, self-starter with strong mechanical aptitudeAbility to work both independently and collaboratively across multiple disciplines in a fast-paced and dynamic environmentExcellent interpersonal, team, and communication skills are a mustHigh level oral and written communication skills are a mustPossess effective task/time management organizational skillsAdditional Qualifications:Applies knowledge and expertise to solve complex technical problemsSignificant contributor to multi-disciplinary teams at the functional levelLed a team or large validation projectsWorking knowledge of process validation, utilities and facilities and analytical equipment/systemsWhy 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.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.Let your curiosity guide your career #BeCurious and explore the endless possibilities at Evotec!The base pay range for this position at commencement of employment is expected to be $115,000 to $126,500; 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.