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The Position

The Hillsboro Technical Operations (HTO) is a drug product and finished goods manufacturing organization responsible for the reliable delivery of Roche’s commercial portfolio & pipeline products. The Manufacturing organization at HTO is divided into Aseptic Operations and Packaging, which combine to produce millions of units of life-saving medicine every year to patients around the world.

Summary:

The Senior Manufacturing Engineer in Aseptic Operations will serve as the technical leader responsible for optimizing, maintaining, and troubleshooting equipment and processes within our sterile manufacturing operations. This individual will drive continuous improvement, support new product introductions, and ensure the robust and compliant production of Roche’s commercial portfolio and pipeline products. A deep understanding of aseptic techniques, cGMP, regulatory requirements, and advanced automation in a sterile environment is paramount for this role.

In this role, you will be an employee of eTeam, working on a Genentech contract.

Shifts:

+ **Night Shifts-Sunday to Tuesday alternating Saturday, 6:00pm to 6:30am**

+ **Night Shifts-Wednesday to Friday alternating Saturday, 6:00pm to 6:30am**

Pay rate (depends on experience): $57/hour to $66/hour

Contract duration:12 months (possible extensions up to 36 months

Key Responsibilities:

+ Collaborate with cross-functional teams, including, Quality, Automation, Process Engineering and Validation to troubleshoot and solve complex problems.

+ Identify and implement process improvements to enhance line efficiency, reduce scrap/rejects, optimize cycle times, and increase yield within the aseptic core and downstream areas.

+ Troubleshoot and resolve technical issues in a timely manner.

+ Provide expert engineering support for complex manufacturing deviations, non-conformances, and quality events specific to aseptic processing.

+ Design and develop mechanical systems, components, and products using advanced engineering principles and techniques.

+ Proven ability to apply structured problem-solving techniques (e.g., 8D, Fishbone, 5 Whys, FMEA) to complex, high-impact manufacturing and sterility-related issues.

+ You will manage documentation including deviations, work orders, work instructions and SOP’s.

Who you are:

+ You have a Bachelors degree (preferably engineering or related field) plus 5 - 10 years experience as an engineer in related industry.

+ Excellent problem-solving skills and attention to detail.

+ You are a self-motivated teammate with the ability to work, prioritize, and deliver results with minimal supervision.

+ You have a demonstrated success operating in teams (especially multi-functional teams)

+ You have strong organizational, computer, and analytical skills.

+ You have experience in equipment maintenance/operation, troubleshooting, and projects.

+ You have an understanding of drug product and/or finished goods processes & equipment

+ Knowledge of use of Computerized Maintenance Management Systems

+ Ability to work in a controlled and aseptic cleanroom environment, strictly adhering to gowning and sterility requirements.

+ May require occasional lifting of up to 25 lbs.

+ Ability to stand, walk, and sit for extended periods; capable of prolonged visual inspection or work at machines.

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants (https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE\_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform) .