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Validation Engineer II

Expired Job

Bayside Solutions Hillsboro , OR 97124

Posted 2 months ago

Bayside Solutions is seeking Validation Engineer II to be part of our client s team in Hillsboro. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients lives. This could explain why their company has been recognized as one of the Top Twenty Employers in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio: Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California.

The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at

Validation Engineer II

Job Benefits:


An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
Work for a company that is local to the bay area and recognized as a leader of innovation.
Competitive compensation commensurate with experience.
This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.
Summary of

Responsibilities:

Support the lead engineer for the Crenuzumab Tech Transfer, by authoring and executing equipment, cleaning and process validation protocols.
Support the validation tactical team by executing requalification/revalidation (RPQ/RCV) activities.
Prepare validation documentation, including protocols, summary reports, etc., for validation activities.
Provide input into validation deviations and participate in root cause analysis.
Coordinate the collection, testing and analysis of samples and reporting of results required per validation protocol.

Required Qualifications:

BS/MS in chemical, biochemical engineering, or related field/experience, with a minimum of 5-7 years experience in drug product Engineering, Manufacturing, or Technical Services is required.
Professional level written and oral communication skills.
Use of Kaye Validator sensing equipment.
Cleaning validation sampling experience, including rinse, swab and visual inspection.
Working knowledge of aseptic manufacturing, isolators, and biologics drug product formulation and filling equipment.



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Validation Engineer II

Expired Job

Bayside Solutions