Onsite QA Document Control Lead - GMP & Compliance

ZP Group; Elkridge (MD); On-site; USD 95,000 - 100,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401K

PTO

Sick Leave and Holidays

Job summary

Piper Companies is currently seeking a QA Document Control Manager for an onsite role in Elkridge, MD. The position sits within a global life sciences organization focused on regulated healthcare products.

The role leads document control, EDMS workflows, and change controls, ensuring cGMP compliance and quality system integrity across departments. It supports audits and quality reporting with cross-functional collaboration.

Qualifications

• Bachelor’s degree or equivalent in a relevant field required.
• Experience in a FDA regulated environment is required.
• 8+ years’ experience in a GMP environment is required.
• Knowledge of cGMP and other regulatory requirements applicable to industry is required.

Responsibilities

• Oversees document control activities to ensure regulatory and cGMP compliance.
• Administers the EDMS, including document workflows, approvals, and change controls.
• Reviews and maintains quality documentation, SOPs, and training records.
• Partners with cross-functional teams to support compliance and process improvements.
• Supports audits, inspections, and quality reporting activities.

Skills

GMP experience

FDA regulated environment

cGMP knowledge

Education

Bachelor’s degree in a relevant area or equivalent work experience

Job description

Piper Companies is currently seeking a QA Document Control Manager for an onsite role in Elkridge, MD. The position sits within a global life sciences organization focused on regulated healthcare products.

The role leads document control, EDMS workflows, and change controls, ensuring cGMP compliance and quality system integrity across departments. It supports audits and quality reporting with cross-functional collaboration.