Manager, Quality Auditing - BB4422 BB4422 Exton, PA 12+ Months Position Summary The Manager, Quality Auditing (Contractor) supports the execution and continuous improvement of the global audit program across the Americas and international operations. This role is responsible for conducting risk-based audits and ensuring that suppliers, partners, and internal sites meet applicable GMP and regulatory requirements. This is a high-impact, independent role requiring deep GMP expertise, strong auditing experience, and the ability to influence stakeholders across a global network. The contractor will conduct external audits of contract manufacturers (CMOs), laboratories, warehouses, and material/service providers, as well as internal audits of company sites. Audits may be performed onsite, remotely, or via desktop review. Responsibilities Audit Program Support, Execution & Oversight Lead and perform risk-based external audits of CMOs, laboratories, warehouses, and suppliers supporting commercial and clinical products Conduct internal audits of company sites to ensure ongoing GMP compliance and inspection readiness Support global audit program execution, including cross-regional audit initiatives Contribute to the development and maintenance of: oGlobal audit schedules oApproved supplier lists oAudit procedures and tools Support training and onboarding of global auditors Identify and communicate trends, risks, and lessons learned from audit findings Participate in inspection readiness activities and support regulatory agency inspections (e.g., FDA, EMA) as needed Reporting & Compliance Independently author clear, concise, and timely audit reports Evaluate supplier responses and ensure appropriate follow-up and closure Manage audit-related records in quality systems (e.g., TrackWise or equivalent) Supplier Quality & Stakeholder Partnership Assess supplier suitability and GMP compliance for new and existing partnerships Partner with Quality, Manufacturing, and Supply Chain stakeholders to resolve supplier quality issues Provide quality input for supplier selection, qualification, and ongoing oversight

Must Have:

The management team has indicated two areas of experience that are particularly critical for the role:

• leading audits in a sterile manufacturing and biologics environment and

• software validation and computerized systems compliance TechData is now a part of Quantive Intelligence, same people, expanded capabilities and we are proud to be an equal opportunity workplace and an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Job Types:

Contract, Temporary Pay:

$50.00 - $70.00 per hour Expected hours: 40.0 per week

Benefits:

Health insurance Application Question(s): What city and state do you currently reside in? What hourly rate are you seeking on a W2? What city and state do you reside in?

Education:

Bachelor's (Required)

Experience:

Quality audits: 3 years (Required) Leading Audits in

Sterile Manufacturing:

1 year (Required) Audit in

Biologics Environment:

1 year (Required)

Software Validation:

1 year (Preferred)

Computerized System Compliance:

1 year (Preferred)

Manufacturing Audits:

3 years (Required)

GMP:

1 year (Required)

Work Location:

In person