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Job Requirements of Quality Control Associate:
-
Employment Type:
Full-Time
-
Location:
Hillsboro, OR (Onsite)
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Quality Control Associate
Tailored Management Services Inc
Hillsboro, OR (Onsite)
Full-Time
Job Title: Quality Control Associate
Location: 4625 NE Brookwood Parkway, Hillsboro, OR 97124
Duration: 6-Month Contract (Potential for Extension or Conversion)
Pay Rate: $25.00 - $29.47/hour (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
About the Role
Key Responsibilities
Qualifications & Requirements
Work Environment & Physical Requirements
Location: 4625 NE Brookwood Parkway, Hillsboro, OR 97124
Duration: 6-Month Contract (Potential for Extension or Conversion)
Pay Rate: $25.00 - $29.47/hour (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage
About the Role
- This position is part of the Analytical Development Quality Control (ADQC) team within the Pharma Technical Cell and Gene Therapy (PTC) organization. The role supports the development of innovative cell and gene therapies by performing analytical development and quality control (QC) activities.
- You will implement analytical methods and perform QC operations to ensure product quality, consistency, and compliance with cGMP standards. This role involves close collaboration with cross-functional and global teams to support clinical development and commercial readiness.
Key Responsibilities
- Execute analytical method validation, qualification, and transfer to support GMP production
- Perform QC testing in compliance with SOPs, specifications, and cGMP regulations
- Conduct assay validation, transfer, and troubleshooting
- Support analytical testing for process development, in-process controls, and product release
- Review and analyze data against established acceptance criteria
- Identify and investigate deviations, discrepancies, and technical issues
- Prepare and review technical documents, including protocols and reports
- Perform equipment qualification, maintenance, and computer system validation
- Maintain laboratory standards, controls, and materials
- Support environmental and utility monitoring activities
- Participate in audits, inspections, and continuous improvement initiatives
- Collaborate with internal teams and global stakeholders
- Ensure timely completion of assigned tasks and project milestones
Qualifications & Requirements
- Bachelor's degree with 2+ years of experience OR Master's degree with 1+ year of experience
- Flow cytometry experience and GMP experience are both critical to the role.
- Preferred fields: Chemistry, Biochemistry, Molecular Biology, or related scientific discipline
- Experience in pharmaceutical or biopharmaceutical industry preferred
- Knowledge of cGMP regulations and quality standards
- Strong analytical, problem-solving, and critical thinking skills
- Ability to work independently and manage multiple priorities
- Strong verbal and written communication skills
Work Environment & Physical Requirements
- Laboratory and office-based role
- Prolonged sitting/standing at lab bench or computer
- Ability to lift up to 25 lbs
- Frequent bending, reaching, and use of lab equipment
- Use of stepladders and pushcarts as needed
- May require travel to other sites
- Must pass visual screening requirements
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