Validation Engineer, QC Lab Equipment (Pharma, cGMP)

Intellectt INC; California (MO); On-site; USD 90,000 - 120,000; Full time

Job summary

Intellectt INC is seeking a Validation Engineer to support qualification activities for QC laboratory equipment in a regulated pharmaceutical/biopharmaceutical environment. Located in California, this 12-month W2 contract role collaborates with laboratory teams, vendors, and stakeholders to ensure equipment is properly qualified and documentation meets quality standards.

The role requires a BS in Engineering/Science, 2+ years in validation, and familiarity with cGMP.

Qualifications

• Bachelor's degree in Engineering, Science, or other technical field.
• 2+ years of experience in validation or equipment qualification.
• Pharmaceutical/biopharmaceutical industry experience preferred.
• Understanding of cGMP and regulated laboratory environments.
• Strong organizational and time-management skills.
• Ability to prioritize multiple activities and meet project timelines.
• Strong problem-solving and communication skills.
• Willingness to adjust working hours as required.

Responsibilities

• Lead or support qualification activities for QC laboratory equipment.
• Partner with laboratory users to define equipment qualification requirements.
• Prepare, review, and execute qualification protocols and docs.
• Coordinate qualification work with vendors and cross-functional teams.
• Evaluate quality issues and assist with corrective actions.
• Review qualification records and documentation per procedures.
• Support laboratory operations and continuous improvement.
• Take on additional validation assignments as needed.

Skills

Organizational skills

Time management

Problem solving

Communication skills

Education

Bachelor's degree in Engineering/Science

Job description

Intellectt INC is seeking a Validation Engineer to support qualification activities for QC laboratory equipment in a regulated pharmaceutical/biopharmaceutical environment. Located in California, this 12-month W2 contract role collaborates with laboratory teams, vendors, and stakeholders to ensure equipment is properly qualified and documentation meets quality standards.

The role requires a BS in Engineering/Science, 2+ years in validation, and familiarity with cGMP.