PSC Biotech
Rockville, United States | Posted on 08/19/2025
At PSC Biotech, we provide the life sciences industry with expert engineering, technical, and consulting services that drive operational excellence, ensure regulatory compliance, and enhance productivity.
Your Role
Our CQV Project Managers deliver comprehensive support to clients throughout every stage of the CQV lifecycle. They offer expert guidance in project planning, strategic development, and execution, employing a risk-based methodology to ensure adherence to regulatory standards and the highest levels of product safety. This is a W2-Temp 6-month role with potential FTE extension.
Requirements
Bachelor's degree in a related engineering discipline. 10 years of commissioning, qualification, and validation experience in the pharmaceutical industry. Experience managing full CQV lifecycle projects. Highly skilled in project planning and scheduling, budget management, risk mitigation, stakeholder communication, and vendor/contractor coordination. Well-versed in CQV risk-based approaches. Expertise in industry regulations, requirements, and guidelines. Proven success in project planning, initiation, execution, and closure. Strong attention to detail and commitment to quality and compliance. Strong problem-solving and analytical skills. Willingness to travel as required. Many projects and clients are located across various regions, and the ability to adapt to different locations, cultures, and work environments is essential for effective collaboration. W2 Temp positions include our medical and sick time benefits. Equal Opportunity Employment Statement: PSC is committed to a policy of Equal Employment Opportunity, complying with all applicable laws concerning employment discrimination. Our policy prohibits discrimination against qualified employees, interns, and applicants in all aspects of employment, including recruitment, hiring, evaluation, compensation, promotion, and termination. Employment decisions are made without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, genetic information, or any other protected status.
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Bachelor's degree in a related engineering discipline. 10 years of commissioning, qualification, and validation experience in the pharmaceutical industry. Experience managing full CQV lifecycle projects. Highly skilled in project planning and scheduling, budget management, risk mitigation, stakeholder communication, and vendor/contractor coordination. Well-versed in CQV risk-based approaches. Expertise in industry regulations, requirements, and guidelines. Proven success in project planning, initiation, execution, and closure. Strong attention to detail and commitment to quality and compliance. Strong problem-solving and analytical skills. Willingness to travel as required. Many projects and clients are located across various regions, and the ability to adapt to different locations, cultures, and work environments is essential for effective collaboration. W2 Temp positions include our medical and sick time benefits. Equal Opportunity Employment Statement: PSC is committed to a policy of Equal Employment Opportunity, complying with all applicable laws concerning employment discrimination. Our policy prohibits discrimination against qualified employees, interns, and applicants in all aspects of employment, including recruitment, hiring, evaluation, compensation, promotion, and termination. Employment decisions are made without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, genetic information, or any other protected status.
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