Senior Validation Engineer - GMP/CQV Specialist

Actalent; Saint Paul (MN); On-site; USD 55,000 - 72,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) plan

Paid time off

Job summary

Actalent is seeking a Validation Engineer for a contract-to-hire role based in Saint Paul, MN. You will prepare, execute and review commissioning, qualification, and validation activities across processes, materials, equipment, cleaning, and computerized systems in a cGMP setting.

Responsibilities include supporting GMP assessments, risk analyses, and traceability matrices while collaborating with project teams to manage multiple validation priorities and lifecycle activities.

Qualifications

• Bachelors degree in Engineering or relevant field or equivalent experience.
• Minimum 3-5 years qualification/validation experience in regulated environments.
• Experience with GMP and equipment life cycle management is preferred.

Responsibilities

• Prepare, review and execute commissioning, qualification, and validation documents.
• Support GMP impact assessments, traceability matrices, and risk assessments.
• Assist in troubleshooting, root cause investigations, and deviation resolution.
• Coordinate with project teams to manage multiple validation priorities in manufacturing.

Skills

Validation

Validation protocols

GMP

Equipment validation

Education

Bachelor's degree in Engineering

Tools

Microsoft Office

Job description

Actalent is seeking a Validation Engineer for a contract-to-hire role based in Saint Paul, MN. You will prepare, execute and review commissioning, qualification, and validation activities across processes, materials, equipment, cleaning, and computerized systems in a cGMP setting.

Responsibilities include supporting GMP assessments, risk analyses, and traceability matrices while collaborating with project teams to manage multiple validation priorities and lifecycle activities.