Process Engineer II - Downstream - Site Based, Redmond, WA

Evote; Union Hill-Novelty Hill (WA); On-site; USD 80,000 - 90,000; Full time

Benefits offered by this job

Discretionary annual bonus

Comprehensive benefits

401(k) company match

Flexible work

Generous paid time off

Wellness benefits

Job summary

Evote is seeking a passionate Process Engineer II located in Union Hill-Novelty Hill, Washington. In this role, you'll drive impactful projects in collaboration with multidisciplinary teams while utilizing your engineering skills to support clinical-scale cGMP manufacturing processes.

Your responsibilities will include developing process understanding, authoring process-related documentation, and utilizing your expertise in downstream purification activities. The position offers a competitive salary range of $80,000 to $90,000 along with comprehensive benefits.

Qualifications

• 2+ years of pharmaceutical/biotech experience.
• Minimum of 2-4 years supporting downstream purification activities.
• Excellent verbal and written communication skills in English.

Responsibilities

• Represent site MSAT on project teams as technical SME.
• Authorship of process-related documentation.
• Drive implementation of CAPAs from approval to closure.

Skills

Technical purification operations

Collaboration

Leadership

Risk management

Communication skills

Education

Masters (or Bachelors) degree in Engineering

Job description

Process Engineer II

We’re looking for a passionate and curious Process 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 Process 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 Process Engineer II Downstream for Site MSAT is part of a fast‑paced, collaborative, and multidisciplinary team. The role reports to Downstream Lead for site MSAT and is responsible for supporting all aspects of downstream processing for multiple clinical‑scale cGMP manufacturing trains employing the innovative Just‑Evotec continuous processing platform in 24/7 operations.

Roles and responsibilities

• Represents site MSAT on project teams as technical subject matter expert (SME) and interface with global MSAT, Operations and Quality functions.
• Develop process understanding and expertise.
• Authors, reviews and owns process related documentation (technical documents, test protocols, batch records, process descriptions, SOPs, etc.)
• Authors, reviews change controls including managing change implementation of the change as the assigned change agent.
• Utilize technical skills and process knowledge to participate and/or lead investigations related to process/new product implementation. Collaborate with impacted groups to drive implementation of CAPAs from approval to closure & effectiveness check.
• Monitors and reports on process performance data analysis.
• Ability to share 24/7 on call support activities during production.
• Apply Operational Excellence principles to lead continuous improvement for downstream process improvements.

Position Requirements

• Masters (or Bachelors) degree in Engineering with 2+ (5+) years of pharmaceutical/biotech experience including a minimum of 2-4 years supporting downstream purification activities for biopharmaceutical products.
• 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.
• Good interpersonal, team, and collaborative skills are required.
• Excellent verbal and written communication skills in English; ability to interface with all levels of the organization.
• Experience in leading risk assessment and risk management for pharmaceutical products and processes. Experience in applying principles of Quality by Design.

The base pay range for this exempt position at commencement of employment is expected to be $80,000 to $90,000; 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, 401(k) 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.