Our goal is to redefine IT staffing by embracing diversity and inclusion, connecting clients with exceptional and skilled professionals who bring innovative solutions while fostering an environment where every individual feels valued and empowered to thrive.
Sr. QC Analyst
Type: Contract, W2 only
Duration: 12+ months with possible extension
Location: onsite in Hillsboro, OR
Pay: $30/hr-$43.5/hr, DOE
Available Shifts: Sunday to Wednesday and Wednesday to Saturday, 4x10s* (onboarding and initial training period may require Mon-Fri, 5X8s, shift). Day: 6:30am to 5:00pm. Swing: 11:30am to 10:00pm
Please note that at this time we are unable to sponsor employment authorization (both new and transfer)
A global biotechnology leader is seeking a Sr. QC Analyst to implement, modify, and enforce Quality Control policies, procedures, specifications and testing methods consistent with cGMP, regulations, appropriate compendium, and the companys standards, policies, plans, objectives and procedures.
Responsibilities:
- Do routine sampling, perform, and review a variety of assays in the Quality Control organization in support of in-process, drug product, finished product, raw materials and incoming inspection, and environmental monitoring testing in a cGMP environment.
- Interpret data, troubleshoots, assay failures and equipment issues while adhering to strict guidelines on cGMP documentation.
- Support method validation activities, performance qualifications, method transfers, discrepancy/out-of-specification investigations and collaborate with stakeholders to identify improvement opportunities in technology and business processes.
- Ensure maintenance and calibration of laboratory equipment and systems.
- Provide support during cGMP audits and Health Authority inspections as needed, and follow up on any corrective measures as required.
- Perform any other tasks as requested by Management to support Quality Oversight activities.
Knowledge, Skills and Abilities:
- B.A. or B.S. degree (preferably in Life Science) and at minimum 3 years experience in a cGMP pharmaceutical, biopharmaceutical industry
- Hands-on industrial laboratory experience with aseptic sampling and testing techniques.
- Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
Work Environment/Physical Demands/Safety Considerations:
- Work in office and laboratory environment. Lift up to 25lbs may be required.
- Ability to sit, stand and move within workspace for extended periods. May be required to sit at a computer terminal for extended periods.
We are an Equal Opportunity employer and welcome talent across all aspects of background, orientation, origin, and identity in an inclusive and non-discriminatory way. Applicants receive consideration without bias and based on the relevant qualifications, talents, skills, experiences, and business needs