Validation Engineer

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

Validation Engineer QC Laboratory

Location: California

Contract: 12 Months

Employment Type: W2 Contract

Job Summary

We are seeking a Validation Engineer to support qualification activities for QC laboratory equipment in a regulated pharmaceutical/biopharmaceutical environment. This position will work closely with laboratory teams, vendors, and internal stakeholders to ensure equipment is properly qualified and documentation meets cGMP and company quality standards.

What You'll Do

• Lead or support qualification activities for QC laboratory equipment.
• Partner with laboratory users to establish equipment qualification requirements.
• Prepare, review, and execute qualification protocols and related documentation.
• Coordinate qualification work with equipment vendors and cross-functional teams.
• Evaluate quality and compliance issues and assist with corrective actions.
• Review qualification records and documentation in accordance with established procedures.
• Support laboratory operations and continuous improvement activities.
• Take on additional validation assignments as business needs arise.

What We're Looking For

• Bachelor's degree in Engineering, Science, or another relevant technical field.
• 2+ years of experience in validation or equipment qualification preferred.
• Pharmaceutical or biopharmaceutical industry experience preferred.
• Understanding of cGMP requirements 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 when required to support project needs.