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Job Description -
Linked in is must have !
Job Role - CQV Lead
Duration: 6 Months
Bloomington, Indiana - Onsite
MOI: Skype
We are looking for a highly experienced CQV Lead with over 15 years of expertise in Commissioning,
Qualification, and Validation within the pharmaceutical or biotech industry. This role will be crucial in leading CQV efforts for large-scale capital projects in a GMP-regulated environment, ensuring that systems, equipment, and facilities are compliant, validated, and audit-ready.
Key Responsibilities include:
Job Description -
Linked in is must have !
Job Role - CQV Lead
Duration: 6 Months
Bloomington, Indiana - Onsite
MOI: Skype
We are looking for a highly experienced CQV Lead with over 15 years of expertise in Commissioning,
Qualification, and Validation within the pharmaceutical or biotech industry. This role will be crucial in leading CQV efforts for large-scale capital projects in a GMP-regulated environment, ensuring that systems, equipment, and facilities are compliant, validated, and audit-ready.
Key Responsibilities include:
- Leading CQV strategy and execution for capital projects (greenfield/brownfield)
- Developing and reviewing validation lifecycle documents such as URS,