Manual Visual Inspection Consultant

Position: Manual Visual Inspection Consultant

Length: 6+ Month Contract

Please no agencies. Direct employees currently authorized to work in the United States – no sponsorship available.

Must be onsite 5 days/week in Fishers, Indiana

We are seeking an experienced Manual Visual Inspection (MVI) Consultant to support sterile drug product operations. This role will focus on performing and supporting manual visual inspection activities to ensure product quality, compliance with GMP requirements, and adherence to regulatory standards.

• Perform manual visual inspection of sterile injectable drug products (vials, syringes, ampoules) for defects including particulates, cosmetic defects, and container closure integrity issues
• Execute inspection activities in accordance with GMP, SOPs, and regulatory requirements
• Document inspection results accurately and in real time within approved systems
• Support inspection-related deviations, investigations, and CAPAs
• Participate in qualification and requalification of inspection personnel
• Assist with inspection method validation, studies, and continuous improvement initiatives
• Collaborate with Quality, Manufacturing, and Engineering teams to ensure compliant inspection operations
• Support audit readiness and participate in internal and regulatory inspections as needed

• Bachelor’s degree in Life Sciences or related field (or equivalent industry experience)
• 2–5+ years of hands‑on experience performing manual visual inspection in a GMP environment
• Strong understanding of aseptic processing and sterile drug product manufacturing
• Familiarity with FDA, EMA, and ICH regulatory expectations related to visual inspection
• Experience working with SOPs, batch records, and controlled documentation
• Strong attention to detail and ability to maintain focus for extended inspection periods

• Experience with inspection qualification programs and defect libraries
• Exposure to automated or semi‑automated inspection systems (a plus)
• Prior experience supporting regulatory inspections
• Background in parenteral manufacturing (vials, prefilled syringes, cartridges)

POST-OFFER BACKGROUND CHECK IS REQUIRED. Digital Prospectors is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Digital Prospectors affirms the right of all individuals to equal opportunity and prohibits any form of discrimination or harassment.

• 4.9/5 Star Glassdoor rating and the only staffing company (< 1000 employees) to be voted in the national Top 10 ‘Employee’s Choice - Best Places to Work’ by Glassdoor.
• Voted ‘Best Staffing Firm to Temp/Contract For’ seven times by Staffing Industry Analysts as well as a ‘Best Company to Work For’ by Forbes, Fortune and Inc. magazine.

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