Job Overview
PSC Biotech is a leading provider of life sciences services, ensuring that healthcare products meet the highest regulatory standards. We strive for client success and offer a collaborative environment with opportunities for growth.
Responsibilities
* Commission, qualify, and validate GxP facilities, equipment, and utilities in assigned projects.
* Draft, execute, review, and approve validation documentation, adhering to cGMP requirements, regulatory standards, and quality protocols.
The ideal candidate will work alongside our talented team in a dynamic biotechnology landscape, driving innovation and excellence. Key Skills:
* Validation and qualification of facilities, equipment, and utilities.
* Critical thinking and problem-solving.
* Excellent communication and collaboration skills.
* Familiarity with GxP regulations and quality protocols.
We offer a competitive compensation package, including benefits such as health insurance, retirement plans, and paid time off. Our employees also enjoy access to professional development opportunities, flexible work arrangements, and a positive work-life balance.
In this role, you will have the opportunity to make a meaningful contribution to our organization's mission and values. If you are a motivated and detail-oriented individual who is passionate about validation and quality assurance, we encourage you to apply.