Quality Engineer
Job in
Hillsboro, Washington County, Oregon, 97123, USA
Listed on 2026-07-13
Listing for:
Dawar Consulting
Full Time
position Listed on 2026-07-13
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
Quality Engineer
Our client, a world leader in diagnostics and life sciences, is looking for a Quality Engineer based out of Hillsboro, OR. Job Duration:
Long term Contract (Possibility Of Further Extension) Pay Rate: $65/hr on W2 Company Benefits:
Medical, Dental, Vision, Paid Sick leave, 401K
The Quality Validation Engineer/Specialist will provide quality oversight and guidance for the site's qualification and validation program, ensuring compliance with cGMP and quality standards.
Key Responsibilities:
- Provide quality oversight of qualification and validation activities for equipment, facilities, utilities, manufacturing processes, cleaning, sterilization, analytical methods, and computerized systems.
- Review, assess, and approve validation and qualification documentation, including protocols, reports, and change controls.
- Evaluate and approve changes impacting validated state and participate in deviation assessments.
- Ensure adherence to internal quality system requirements and regulatory expectations.
- Collaborate cross-functionally to drive compliant, consistent, and efficient validation practices.
- Apply sound technical judgment in resolving complex quality and validation issues.
Qualifications:
- Bachelor's degree in Engineering, Life Sciences, or related field.
- 5–10 years of experience in the biopharmaceutical or pharmaceutical industry with focus on validation or quality assurance.
- Strong knowledge of qualification/validation principles and lifecycle approach.
- In-depth understanding of cGMPs and health authority expectations.
- Excellent analytical, problem-solving, and communication skills.
- Ability to work effectively across functions and adapt to changing priorities.
Top
Skills:
Qualification & Validation (Equipment, Process, Cleaning, CSV) cGMP Compliance & Quality Systems Risk Assessment, Change Control, and Deviation Management
If interested, please send us your updated resume at /
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