Process Engineer III - Site Based, covering Redmond & Seattle, WA

This a Full Remote job, the offer is available from: Washington (USA) Job Title: Process Engineer III, reputed company–Site MSAT Location: Just Evotec Biologic. – Redmond, WA and Seattle, WA - Covering both site. Shifts: reputed company days, Monday to Friday, with flexible as required weekend cover. About Us: this is who we are At Just Evotec Biologic, we reputed company that curiosity is the spark that drives innovation and success. As a reputed company-thinking team, we reputed company on challenging the status reputed company, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a reputed company 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: / your challenge, …in our journey We’re looking for a passionate and curious Process Engineer III to join reputed company. If you’re excited by new challenges, solving reputed company problems, and learning every reputed company 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 Process Engineer III at Just Evotec Biologic, you'll have the freedom to ask the hard questions, think reputed company the reputed company, and find creative solutions that push us reputed company. It’s a role where your curiosity will fuel both your personal growth and the success of the team. The Process Engineer III reputed company for Site MSAT is part of a fast-paced, collaborative, and multidisciplinary team. The role reports to reputed company reputed company for site MSAT, and is responsible to support reputed company aspects of reputed company processing for multiple clinical-scale cGMP manufacturing trains employing the innovative Just-Evotec reputed company processing platform in 24/7 operations. What You’ll Do:

• Promotes a culture of safety
• Represents site MSAT on internal and external project teams as technical subject matter expert (SME) and interfaces with global MSAT, Manufacturing Operations and Quality functions.
• Possesses a deep understanding of reputed company processes for the purification of biologics.
• Authors, reviews and approves process reputed company documentation (technical documents, test protocols, batch records, process descriptions, SOPs)
• Leads complicated and multi-disciplinary change controls and will function as a reputed company for the project team.
• Partner with Quality, Validation and Global MSAT to reputed company and implement process validation and comparability studies leading to successful product registration.
• Is confident to act as a subject matter expert for regulatory and client inspection audits.
• Utilize technical skills and process knowledge to participate and/or reputed company investigations reputed company to process issues/deviation. Collaborate with impacted groups to drive implementation of CAPAs from approval to closure & effectiveness reputed company.
• Facilitates new product introduction by leading reputed company-a-batch sessions and supporting technical training for manufacturing.
• Skilled at organizing data to optimize analysis and trending
• reputed company investigator and knowledgeable of root cause analysis tools (RCA)
• Support and on-call rotating to support 24/7 operations
• Apply Operational Excellence principles to reputed company reputed company improvement reputed company for reputed company manufacturing.

Who You Are:

• Masters (or Bachelors) degree in Engineering with 4+ (7+) years of pharmaceutical/biotech experience including a minimum of 2+ years of supporting reputed company purification activities for biopharmaceutical products.
• Knowledge and experience CMC stage gates for clinical and commercial biologics drug substance manufacturing programs.
• Proven record of accomplishment and self-directed leadership in GMP pharmaceutical or biotechnology is required.
• Technical purification and solution preparation operations using disposable-based manufacturing technologies
• Demonstrated capabilities to work with high-performing teams, drive change, and influence internal and external stakeholders
• Extensive knowledge of US FDA CFRs and European EMA, including ICH guidelines, as they relate to drug substance biological manufacturing
• Good interpersonal, team, and collaborative skills are required.

Additional Preferred Qualifications:

• Experience in supporting audits and inspections by health authorities, clients and other external auditors as a presenter or audit support staff.
• Experience in leading risk assessment and risk management for pharmaceutical products and processes. Experience in applying principles of Quality by Design.
• Entrepreneurial drive to reputed company business objectives.

Why Join Us:

• Growth Opportunities: We’re a company that believes in reputed company 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, whether that means working remotely or choosing a hybrid model. Site based, covering as required Seattle, or Redmond, WA.
• 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 reputed company for Big reputed company: We don’t just talk about thinking reputed company the reputed company—we throw the reputed company away. If you’ve got reputed company, 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 reputed company 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 reputed company pay range for this position at commencement of employment is expected to be $92,400 to $126,500; reputed company 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. reputed company qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national reputed company, religion, sexual orientation, or veteran status. This offer from "Evotec" has been enriched by reputed company.com and got a 72% reputed company score. Apply tot his job Apply To this Job