Lead the CQV Program at BIOVECTRA ensuring compliance in a full-time role. Oversee commissioning and qualification of Facilities, Utilities, and Equipment while maintaining validated states throughout their lifecycle.
As a CQV Supervisor, you will provide technical leadership within a dynamic team at BIOVECTRA. Collaborate cross-functionally with multiple departments including Engineering, Manufacturing, and Quality to support compliance and continuous improvements. This role demands expertise in GMP systems and hands-on experience in commissioning and qualification.
Key Responsibilities: • Lead Facilities, Utilities,
and Equipment CQV Program • Develop and maintain CQV schedules and prioritize activities • Plan and oversee lifecycle management activities • Review and approve various CQV documentation • Monitor regulatory compliance and implement improvements
Requirements: • Bachelor’s degree in a technical discipline • Minimum three years in a GMP setting • Experience in CQV, validation, and quality systems • Strong technical writing and problem-solving skills • Supervisory experience is a plus
Elevate the CQV program by using your leadership and technical expertise in this vital role at BIOVECTRA. #J-18808-Ljbffr