CQV Specialist

Intellectt INC; United States; On-site; USD 120,000 - 155,000; Full time

Job summary

Intellectt INC is seeking an experienced CQV Specialist to support commissioning, qualification, and validation activities in a GMP biomanufacturing environment in Brooklyn Park, MN.

You will focus on IQ/OQ/PQ protocols, deviations, investigations, CAPA, and the qualification of bioreactors, vessels, fill-finish lines, CIP/SIP systems, collaborating with Engineering, Manufacturing and Quality teams to ensure audit readiness.

Qualifications

• 10+ years of CQV, validation, quality, or engineering experience in pharmaceutical, biotech, or life sciences environments.
• Experience authoring and executing IQ/OQ/PQ protocols.
• Experience with deviations, investigations, and CAPA in GMP environments.
• Strong technical writing and communication skills.

Responsibilities

• Author and execute IQ/OQ/PQ protocols and validation reports.
• Support commissioning, startup, and qualification activities.
• Write and investigate CQV-related deviations and support CAPA.
• Support qualification of bioreactors, vessels, fill-finish lines, transfer panels, CIP/SIP systems, process utilities.
• Support risk assessments, change controls, and project documentation.
• Collaborate with Engineering, Manufacturing, Quality, and Validation teams.
• Support audit and regulatory inspection readiness.

Skills

CQV

Validation

Quality

Engineering

Technical writing

Communication

Education

Bachelor's degree in Engineering, Life Sciences, Biotechnology, or a related field

Job description

Job Title: CQV Specialist

Location: Brooklyn Park, MN

Duration: 12-Month

Employment Type: W2

Job Summary

Seeking an experienced CQV Specialist to support commissioning, qualification, and validation activities in a GMP biomanufacturing environment. The role will focus on equipment qualification, validation protocols, deviations, and investigations across upstream and fill-finish systems.

Responsibilities

• Author and execute IQ/OQ/PQ protocols and validation reports.
• Support commissioning, startup, and qualification activities.
• Write and investigate CQV-related deviations and support CAPA.
• Support qualification of bioreactors, vessels, fill-finish lines, transfer panels, CIP/SIP systems, and process utilities.
• Support risk assessments, change controls, and project documentation.
• Collaborate with Engineering, Manufacturing, Quality, and Validation teams.
• Support audit and regulatory inspection readiness.

Requirements

• Bachelor's degree in Engineering, Life Sciences, Biotechnology, or a related field.
• 10+ years of CQV, Validation, Quality, or Engineering experience in pharmaceutical, biotech, or life sciences environments.
• Experience authoring and executing IQ/OQ/PQ protocols.
• Experience with deviations, investigations, and CAPA in GMP environments.
• Knowledge of FDA, cGMP, and validation requirements.
• Strong technical writing and communication skills.
• Ability to work onsite in Brooklyn Park, MN.