You will perform testing and related work in the Product Analytical and Bioassay Testing (PABT) organization on in-process, drug substance, and drug products for release or stability programs. Perform laboratory testing in a cGMP environment and understand the science and compliance needs of the business. Actively participate in continuous improvement to maintain the company’s right to operate, supply to patients, and cost-effectiveness. What you will do: Be an active and visible change agent. P... more details
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche!
The Opportunity:
You will perform testing and related work in the Product Analytical and Bioassay Testing (PABT) organization on in-process, drug substance, and drug products for release or stability programs. Perform laboratory testing in a cGMP environment and understand the science and compliance needs of the business. Actively participate in continuous improvement to maintain the company’s right to operate, supply to patients, and cost-effectiveness.
- Be an active and visible change agent
- Perform a variety of basic and moderate complex lab tests
- Perform testing of routine and non-routine samples and documents according to cGMPs
- Perform routine lab maintenance
- Prepare basic and complex reagents as assigned
- Independently manage competing priorities with limited instruction
- Identify and recommend solutions to potential procedural, process system gaps
- Participate in assay transfer and assay validation
- Perform equipment qualification/maintenance
- Maintain a state of inspection readiness
- Adhere to cGMP policies and procedures, including documentation activities
Who you are:
- QC Associate I: B.S./B.A.and 2+ years of experience in the pharmaceutical industry
- QC Associate II: B.S./B.A.and 4+ years of experience in the pharmaceutical industry
- Knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
- Ability to exercise sound judgment, reasoning, and problem-solving.
- Capable of completing assigned responsibilities and keeping the manager informed of status.
- Extensive knowledge and technical understanding to complete routine and non-routine assignments.
Safety Considerations:
Work is performed in a laboratory setting. Exposure to hazardous chemicals may occur. Work requires use of glassware, needles, syringes, and hot plates. PPE (e.g. lab coat, safety glasses) is required whenever working in the laboratory.
Relocation benefits are not available for this position.
The expected salary range for this position based on the primary location of Vacaville, CA for QC Associate I is $54,000 to $104,000 and for the QC Associate II is $91,000 to $118,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors (Overtime) permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
Benefits
NOTE: The Roche site at Vacaville is in an agreement to divest. This position could be transferred to the acquiring company.
Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us. Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.
