QA Batch Release & Disposition Manager

Resilience US; Olde West Chester (OH); On-site; USD 120,000 - 170,000; Full time

Job summary

Resilience US is a technology-focused biomanufacturing company seeking a Manager, QA Batch Disposition to lead batch release and disposition operations, oversee GMP documentation review, and build robust disposition processes across process nodes. You will mentor a batch release team, coordinate with clients, and ensure timely, compliant release decisions.

The ideal candidate has hands-on QA leadership experience in pharmaceutical manufacturing, deep cGMP knowledge, and a track record of

Qualifications

• Experience leading QA teams and driving batch disposition decisions.
• Strong knowledge of cGMP requirements and regulatory expectations.
• Proven ability to collaborate across functions (QA, Manufacturing, Validation, Supply Chain).

Responsibilities

• Manage and lead the batch release team during disposition and review GMP documentation.
• Provide QA support for projects and coordinate with customers and internal groups to resolve quality issues.
• Maintain partnerships with clients to meet project timelines, product quality, and GMP compliance.
• Collaborate with Manufacturing Operations and support functions to ensure efficient batch disposition operations.
• Direct and develop QA personnel, including performance management and coaching.
• Review and approve GMP records (Change Controls, batch records, material disposition, deviations).
• Support technical transfers, validation plans/protocols, SOPs, and risk assessments.
• Oversee release of incoming materials (bulk, APIs, excipients, packaging components).
• Ensure GMP compliance in planning, execution, and closeout of improvement projects.

Skills

People leadership

cGMP knowledge

Quality systems

Pharmaceutical manufacturing

Education

Bachelor's degree or higher

Job description

Resilience US is a technology-focused biomanufacturing company seeking a Manager, QA Batch Disposition to lead batch release and disposition operations, oversee GMP documentation review, and build robust disposition processes across process nodes. You will mentor a batch release team, coordinate with clients, and ensure timely, compliant release decisions.

The ideal candidate has hands-on QA leadership experience in pharmaceutical manufacturing, deep cGMP knowledge, and a track record of