QA Batch Disposition Lead - Quality & Release

Resilience; Ohio; On-site; USD 95,000 - 144,000; Full time

Benefits offered by this job

Annual bonus program

401(k) company match

Health, dental and vision insurance

Paid vacation and holidays

Tuition reimbursement

Job summary

Resilience, Inc. is seeking a Manager, QA Batch Disposition in West Chester, OH. You will lead the batch release team, oversee GMP documentation review, and ensure quality and client-facing communication throughout disposition processes.

The role requires advanced cGMP knowledge, leadership experience in QA, and collaboration across cross-functional teams to support regulatory compliance and continuous improvement.

Qualifications

• Experience in a leadership role within QA or quality assurance.
• Advanced knowledge of cGMP requirements, quality systems, and pharmaceutical manufacturing/packaging technologies.
• Ability to influence leaders in a matrix environment and make patient-safety-driven decisions.
• Strong familiarity with regulatory agency interactions and compliance procedures.

Responsibilities

• Provide direction and leadership to the batch release team during disposition of batches and GMP documentation review.
• Ensure QA support for internal and external projects and timely client communications.
• Maintain strong client partnerships and ensure project timelines and product quality meet GMP compliance.
• Collaborate with Manufacturing Operations and other support functions to sustain batch disposition operations.
• Oversee QA review and approval of changes, deviations, investigations, and tech transfers.

Skills

People leadership

cGMP knowledge

Quality systems

Regulatory interactions

Problem solving

Cross-functional teamwork

Education

Bachelor’s degree or higher

Job description

Resilience, Inc. is seeking a Manager, QA Batch Disposition in West Chester, OH. You will lead the batch release team, oversee GMP documentation review, and ensure quality and client-facing communication throughout disposition processes.

The role requires advanced cGMP knowledge, leadership experience in QA, and collaboration across cross-functional teams to support regulatory compliance and continuous improvement.