Biorepository Operations Lead

Azenta Life Sciences; Indianapolis (IN); On-site; USD 65,000 - 88,000; Full time

Job summary

Azenta Inc. is seeking a Supervisory leader for Biorepository Operations in the United States. You will supervise the Biobank team, manage daily activities, and ensure quality and process improvements across shifts and departments.

Responsibilities include setting goals, enforcing policies, coordinating sample receipt, storage, and data entry, and guiding staff through performance reviews and development. Prior experience in GMP/GLP environments is preferred.

Qualifications

• Bachelor’s Degree in a related field with 2+ years of people and functional experience or equivalent
• Experience in FDA-regulated environments is preferred
• Experience in sample and/or data management is preferred

Responsibilities

• Set and communicate goals and objectives for the Biobank team.
• Promote collaboration across shifts, teams and departments.
• Manage personnel, productivity, inventory, metrics and resources.
• Enforce policies and ensure quality compliance.
• Provide reports and documentation to leadership as needed.
• Oversee receipt, accessioning and storage of samples.
• Drive continuous process improvement and corrective actions.

Skills

Leadership

Team coordination

Communication

Education

Bachelor’s Degree + 2 years people/functional experience

Associate Degree + 4 years, 2 years in people/functional experience

HS Diploma + 5 years, 2 years people/functional experience

1 year experience as a Team Coordinator at Azenta

FDA-regulated industry experience

Tools

GMP/GLP knowledge

Job description

Azenta Inc. is seeking a Supervisory leader for Biorepository Operations in the United States. You will supervise the Biobank team, manage daily activities, and ensure quality and process improvements across shifts and departments.

Responsibilities include setting goals, enforcing policies, coordinating sample receipt, storage, and data entry, and guiding staff through performance reviews and development. Prior experience in GMP/GLP environments is preferred.