The QC Tech I performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, environmental monitoring, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties.
Performs test methods as written to support product/material release.
Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.
Will perform a multitude of laboratory techniques for which they are trained.
Accepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives.
Revises procedures as necessary and provides support for department.
Support investigations
Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.
Associates Degree in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree with <2 years pertinent experience or High School Diploma with 2+ years combined experience in Manufacturing, QA, QC, R&D in pharmaceutical or biologics industry.
Maintains their certifications as needed for assigned job tasks.
Key Stakeholders
Development, Manufacturing, Quality and Regulatory
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