Senior Quality Systems Engineer-GMP Compliance & Validation

United Pharma; Utah; On-site; USD 110,000 - 150,000; Full time

Job summary

United Pharma is seeking a Senior Quality Systems Engineer to strengthen site QMS, GMP compliance, and documentation workflows. The role focuses on validation, qualification, and change management to sustain compliant manufacturing operations.

You will oversee change control processes, review quality records and SOPs, and support continuous improvement and metrics tracking to meet regulatory standards.

Qualifications

• 5+ years in Quality Systems/GMP/compliance within pharmaceutical manufacturing.
• 3+ years QA in pharmaceutical production.
• Bachelor’s degree in biology, chemistry or related field preferred, or equivalent experience.

Responsibilities

• Support and maintain QMS and GMP compliance programs.
• Lead Change Control activities from initiation to final approval.
• Host and facilitate the Change Control Review Board.

Skills

Quality Systems

GMP Compliance

Change Control

Documentation Management

Education

Biology/Chemistry degree

Job description

United Pharma is seeking a Senior Quality Systems Engineer to strengthen site QMS, GMP compliance, and documentation workflows. The role focuses on validation, qualification, and change management to sustain compliant manufacturing operations.

You will oversee change control processes, review quality records and SOPs, and support continuous improvement and metrics tracking to meet regulatory standards.