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 agile 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 environment
- 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.