GMP Document Control Specialist

Haleon; United States; On-site; USD 79,000 - 109,000; Full time

Benefits offered by this job

401(k) plan

Tuition reimbursement

Parental leave

Healthcare coverage

Job summary

Haleon, a leading consumer health company, seeks a Document Control Specialist to ensure regulatory compliance and quality systems across GMP documentation. The role emphasizes documentation lifecycle, system administration, and collaboration with cross-functional teams to maintain audit readiness.

The position offers competitive pay, a comprehensive benefits package, and the opportunity to contribute to Haleon’s global quality culture in the United States.

Qualifications

• Bachelor's degree required in a relevant field.
• 2+ years in a regulated GMP environment.
• Knowledge of quality systems and document control processes.

Responsibilities

• Manage the Document Control Application as Local Business Administrator.
• Support GMP document reviews and lifecycle management.
• Assist in training and support for document authors, reviewers, and approvers.
• Contribute to continuous improvement of quality systems and documentation processes.
• Support audits and inspections related to GMP documentation.

Skills

Document control

GMP compliance

Quality systems

Regulatory awareness

Education

Bachelor's degree (Business Administration, Biology, Microbiology, Chemistry, Biochemistry, Pharmacy or Management)

Job description

Haleon, a leading consumer health company, seeks a Document Control Specialist to ensure regulatory compliance and quality systems across GMP documentation. The role emphasizes documentation lifecycle, system administration, and collaboration with cross-functional teams to maintain audit readiness.

The position offers competitive pay, a comprehensive benefits package, and the opportunity to contribute to Haleon’s global quality culture in the United States.