GMP Data Reviewer - Onsite, Mon-Fri, Quality Impact

Unknown Company; Oakdale (MN); On-site; USD 55,000 - 65,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Pace Analytical in Oakdale, MN is seeking a GMP Data Reviewer to oversee quality records, review data, and ensure compliance with SOPs and regulatory requirements. The role emphasizes collaboration with cross-functional teams to maintain data integrity and support manufacturing operations.

Essential duties include analyzing quality data, mentoring staff on procedures, and contributing to continuous improvement initiatives within a GMP environment.

Qualifications

• Bachelor's degree in chemistry or related field, plus 2–4 years quality experience.
• Experience with complex programs or operations.
• Strong knowledge of quality laws, regulations, and procedures.
• Proficient in English with good communication skills.
• Ability to train others and work in teams.

Responsibilities

• Overseeing, updating, and processing quality records, documents, SOPs, and LIMS data.
• Provide analysis and counsel on quality programs to management.
• Resolve customer feedback and coordinate resources as required.
• Review operations to identify trends and present recommendations.
• Ensure accuracy of tests, equipment, actions, and data via audits.
• Support cross-functional projects with budgets, timelines, and materials.
• Interpret and apply department policies, laws, and regulations.
• Contribute to team efficiency and a harmonious workplace.

Skills

Quality principles

SOP knowledge

LIMS data handling

Documentation skills

Team collaboration

Education

Chemistry degree

Tools

LIMS

Job description

Pace Analytical in Oakdale, MN is seeking a GMP Data Reviewer to oversee quality records, review data, and ensure compliance with SOPs and regulatory requirements. The role emphasizes collaboration with cross-functional teams to maintain data integrity and support manufacturing operations.

Essential duties include analyzing quality data, mentoring staff on procedures, and contributing to continuous improvement initiatives within a GMP environment.