The Fountain Group is currently seeking a Quality Control Technician for a prominent client of ours. This position is located in Hillsboro, OR.
Details for the position are as follows :
Shift Details :
Day Shift during training for 2 months, Monday to Friday, 8 : 00 am to 4 : 30 pm, after training pivots to Sunday to Wednesday, 4 x 10, 7 : 00 am to 5 : 30 pm.
TRAINING (2 months) : Monday-Friday 8am-4 : 30pm SHIFT (4 / 10) : Sunday-Wednesday 7am-5 : 30pm
Job Description :
Overview : Responsibilities include performing and reviewing a variety of assays in the Quality Control organization in support of In-Process intermediates, drug substance, drug product and stability sample testing in a cGMP environment.
Specifically, biochemical assays, using analytical techniques and instrumentation, such as high-performance liquid chromatography (HPLC) and mass spectroscopy.
The QC Associate II must be able to interpret data troubleshoot assay failures and equipment issues while adhering to strict guidelines on cGMP documentation.
In addition, the individual will support cycle development, performance qualifications, method transfers, discrepancy / out-of-specification investigations and collaborate with external groups to identify improvement opportunities in technology and business process.
Responsibilities : Follow company policies and procedures. Maintain a state of inspection readiness. Operate Glassware washer and autoclave.
Independently manage competing priorities with limited instruction. Perform environmental monitoring and water sampling.
Provide assistance to customers in support of departmental functions. Participate in the design and implementation of department and cross-functional initiatives.
Apply basic theory and technical principles to address moderately complex problems. Troubleshoot and initiate the resolution of Quality issues by fostering effective interdepartmental and cross functional partnerships.
Serve as a technical subject matter expert (SME) in support of department functions. Sign documents for activities as authorized and described by Genentech policies, procedures, and job descriptions.
Be accountable for behaviors as described in Genentech's Core, Common, and Critical Competencies. Perform any other tasks as requested by Management to support Quality oversight activities
Qualifications :
- Strong analytical chemistry skillset
- GMP / biotech / pharma experience preferred
Compensation : $20-26 per hour depending on experience