JOB DESCRIPTION:

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 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.

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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.