Join Lonza in Vacaville, CA as a Quality Control(QC) Associate I. You will be a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw materials, and stability lots for customer. Perform a broad variety of basic and moderately complex tests/activities in support of cGMP laboratory operations.
What you will get: The full-time base annual salary for this position is expected to range between $63,750 to $106,250. In addition, below you will find a comprehensive summary of the benefits package we offer:
- Performance-related bonus
- Medical, dental and vision insurance
- 401(k) matching plan
- Life insurance, as well as short-term and long-term disability insurance
- Employee assistance programs
- Paid Time Off
Shift : Back Half Graves: Wednesday to Saturday 6pm-4:30am What you will do : - Collaborate on cross-functional teams to create or improve business processes and resolve problems of moderate scope.
- Perform a variety of basic to moderately complex analytical tests on in-process materials, drug substances, drug products, and raw materials.
- Drive continuous improvement initiatives to optimize product testing and general Quality Control lab operations.
- Utilize technical expertise to lead troubleshooting efforts and support method transfer activities within main operational areas.
- Support cGMP laboratory operations ensuring compliance with company policies and procedures for all customer stability lots.
- Identify and document deviations from accepted practices and participate in the evaluation and assessment of change records.
- Manage quality reagent preparation and inventory to ensure high-quality, on-time testing that meets manufacturing demands.
What we are looking for: - B.S./B.A degree in Life Science or related field.
- Experience is in pharmaceutical or biopharmaceutical industry desirable.
- Maintain strict Data Integrity standards in accordance with Lonza policies while utilizing laboratory computer systems and Microsoft Suite.
- Analyze data and troubleshoot semi-routine problems of moderate scope, identifying any deviations from accepted practices.
- Support cross-functional QC projects and expand responsibilities across diverse functional areas to meet business needs.
