Pharma C&Q Engineer: Commissioning & Qualification

Hyde Engineering + Consulting; Boulder (CO); On-site; USD 75,000 - 110,000; Full time

Job summary

Hyde Engineering + Consulting seeks a Commissioning & Qualification Engineer in Boulder, CO. The role supports process equipment, clean water and CIP systems, and oversees FAT, IQ, OQ, PQ activities and ETOPs.

Responsibilities include documenting deliverables, coordinating protocols, reports and calibration certificates, and ensuring cGMP compliance. Travel within the United States is expected.

Qualifications

• BS degree or higher in chemical engineering or related field, or significant related experience.
• Experience with pharmaceutical manufacturing.
• Ability to create an environment of trust, compliance, continuous improvement and learning.
• Demonstrated ability to manage multiple priorities with aggressive timelines.
• Effective written communication utilizing GDP; effective oral communication; convey information accurately.
• Ability to relate with people at all levels and diverse cultures.
• Willingness to travel within the United States as needed.

Responsibilities

• Support process equipment, cleaning systems, fill/finish equipment, isolators, utilities, HVAC, monitoring systems and facilities.
• Perform tests and reviews including FAT, IQ, OQ, PQ and cycle development protocols and final reports.
• Commission and qualify equipment; provide ETOPs.
• Provide process engineering support for clean water systems, CIP and pharmaceutical process equipment.
• Assist the project lead in delivery and project management to meet timeline and budget.
• Promote cGMP and regulatory compliance on projects.
• Review and modify SOPs for various equipment.
• Document, monitor and report project deliverables; manage protocols and calibration certificates.

Skills

Written comms

GDP compliance

Project coordination

Cross-functional collab

Education

Bachelor's in chemical eng or related

Job description

Hyde Engineering + Consulting seeks a Commissioning & Qualification Engineer in Boulder, CO. The role supports process equipment, clean water and CIP systems, and oversees FAT, IQ, OQ, PQ activities and ETOPs.

Responsibilities include documenting deliverables, coordinating protocols, reports and calibration certificates, and ensuring cGMP compliance. Travel within the United States is expected.