Process Engineer I - Site based Redmond, WA

Evotec WD; Redmond (WA); On-site; USD 78,000 - 83,000; Full time

Job summary

A leading life science company in Redmond, WA is seeking a Process Engineer I to support the design and development of new equipment for their manufacturing network. This role involves collaborating with stakeholders, developing documentation, and ensuring compliance with regulations. Ideal candidates will have a BS in engineering or sciences and relevant experience in cGMP manufacturing. The position offers a competitive salary and benefits.

Benefits

Bonuses

Health Insurance

401k Match

Flexible Work

Paid Time Off

Qualifications

• 0-3 years relevant experience required.
• Knowledge of cGMP manufacturing and regulations for biologics/pharmaceuticals.

Responsibilities

• Support evaluation and implementation of processing technologies.
• Collaborate on design documents and validation protocols.
• Develop quotations and collaborate with procurement.

Skills

Quality Focus

Attention to Detail

Organizational Skills

Interpersonal Skills

Communication Skills

Education

BS in Engineering

BS in Sciences

Tools

DeltaV Automation

Job description

Process Engineer I - Site based Redmond, WA

Process Engineer I - Site based Redmond, WA

Apply locations: Redmond, Seattle, WA | Time type: Full time | Posted on: Posted 3 Days Ago | Job requisition id: JOB ID-12395

The selected candidate for the role of Process Engineer I, as part of the GMSAT Technology team, will support the design and development of new equipment and technologies for the Just-Evotec manufacturing network. Responsibilities include developing support documentation for technology implementation, providing technical and operational support to Site MSAT and Manufacturing Operations groups, and assisting in regulatory submissions and inspections.

Responsibilities (including but not limited to):

1. Support key stakeholders with evaluation and implementation of processing technologies.
2. Collaborate on design documents and validation protocols.
3. Evaluate and design single-use technologies and assemblies.
4. Work with vendors on data and validation packages.
5. Develop quotations and collaborate with procurement.
6. Create business processes, SOPs, and training materials.
7. Support equipment maintenance and lifecycle planning.
8. Partner with Site MSAT Manufacturing Technology & Science teams on objectives.

Position Requirements:

1. BS in engineering, sciences, or related field; 0-3 years relevant experience.
2. Knowledge of cGMP manufacturing and regulations for biologics/pharmaceuticals.
3. Understanding of monoclonal antibody processing.
4. Ability to work independently and in teams.
5. Knowledge of manufacturing equipment and automation systems.
6. Strong focus on quality, attention to detail, and organizational skills.
7. Ability to analyze and communicate process data effectively.
8. Excellent interpersonal and communication skills.

Preferred Qualifications:

1. Experience with single-use manufacturing systems.
2. Experience with DeltaV automation.
3. Participation in global teams or Centers of Excellence.
4. Proficiency in CQV plans and protocols.
5. Ability to lead projects within the team.

This description outlines the general functions and requirements of the job and is subject to change as per the company's needs.

The salary range is $78,000 to $83,000, with additional benefits including bonuses, health insurance, 401k match, flexible work, paid time off, and more.

Evotec (US) Inc. is an Equal Opportunity Employer, providing consideration without regard to race, gender, age, disability, or veteran status.

About Us

Evotec is a life science company focused on discovering and developing therapeutics. It utilizes a data-driven R&D approach, collaborating with top pharma, biotech, and academic institutions globally. With over 5,000 employees and 17 sites, Evotec aims to create a leading pipeline of innovative therapeutics across various underserved areas.