Job Description Job Description
Description:
Shift hours: 06: 00 Am - 02: 30 Pm
Shift days: Monday - Friday (5x onsite)
- Perform a broad variety of basic and moderate complex tests in support of GMP lab operations.
- Responsible for sampling of utility systems and manufacturing process spaces in Vacaville and performing a variety of chemical and microbiological analyses.
- Actively participate in continuous improvement to maintain company's right to operate, supply to patients and cost effectiveness.
Key Responsibilities
- Perform testing of routine and non-routine samples and documents according to GMP.
- Perform routine lab maintenance.
- Understand theory of assays; mentor others in assay/laboratory functions.
- Prepare both basic and complex reagents.
- Identify and troubleshoot technical problems.
- Order and maintain lab supply inventory.
- Coordinate with customers to support operational activities.
- Identify and support resolution of technical problems.
- Participate in group, project teamwork and process improvements.
- Resolve issues as needed with management approval.
- Follow all GMP rules, including accurate documentation.
- Meets scheduled performance of 95% on time.
- Support Quality by completing tasks assigned by the supervisor or manager.
Key Requirements
- BS/BA in Biological Sciences, Physical Sciences, or Engineering preferred.
- Work in office and laboratory environment.
- Strong verbal and written communication skills, ability to organize and present information both formally and informally.
- Proven ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
- Capable of working under moderate supervision and determining own short term priorities.
- Knowledge of computerized management systems, Microsoft Suite, and cGMP awareness is a plus.
