Analytical Equipment Engineer - CQV, GMP & Maintenance

veristainc; Thousand Oaks (CA); On-site; USD 85,000 - 127,000; Full time

Benefits offered by this job

Competitive pay

Medical, Dental & Vision insurances

401(k) Retirement Plan with company‑M

Paid Time Off and Holidays

Tuition Reimbursement

Onsite work in Thousand Oaks

Job summary

Verista is a leading life sciences solutions provider with a strong customer focus in pharmaceutical and biotechnology manufacturing. We are seeking a Project Engineer to support analytical equipment, CQV activities, and ongoing operations across multiple facilities.

The role requires a Bachelor's degree in Engineering or related discipline and 5+ years of hands-on experience in GMP environments. Onsite work in Thousand Oaks, CA, five days a week, with a competitive salary and benefits package.

Qualifications

• Bachelor's degree in Engineering, Biotechnology, Chemistry, or related technical discipline preferred.
• 5+ years of relevant experience supporting analytical equipment in a pharmaceutical, biotechnology, or GMP-regulated manufacturing environment.
• Demonstrated hands-on experience troubleshooting analytical or in-process testing equipment.
• Experience supporting commissioning, qualification, and validation (CQV) of analytical instrumentation.
• Strong understanding of GMP requirements, preventative maintenance, and equipment documentation.
• Proven ability to perform root cause analysis and coordinate technical troubleshooting with equipment vendors.
• Experience providing direct equipment support within an active manufacturing environment.

Responsibilities

• Perform hands-on troubleshooting, root cause analysis, and technical support for analytical equipment used in pharmaceutical and biotechnology manufacturing.
• Lead and support commissioning, qualification, validation (CQV), and decommissioning activities for analytical equipment.
• Coordinate with equipment vendors to resolve technical issues, perform repairs, and improve equipment reliability.
• Execute and manage preventative maintenance activities, equipment inspections, and spare parts inventory.
• Review and maintain qualification documentation, SOPs, equipment records, and associated GMP documentation.
• Perform user access audits, password management, and other equipment compliance activities.
• Collaborate with Analytical, Engineering, Instrumentation, and Manufacturing teams to ensure equipment availability and operational efficiency.
• Develop and execute project plans, schedules, and equipment improvement initiatives.

Skills

Troubleshooting equipment

Root cause analysis

Project management

Strong communication

GMP compliance

Education

Bachelor's degree in Engineering, Biotechnology, Chemistry or related technical discipline

Tools

CQV

Job description

Verista is a leading life sciences solutions provider with a strong customer focus in pharmaceutical and biotechnology manufacturing. We are seeking a Project Engineer to support analytical equipment, CQV activities, and ongoing operations across multiple facilities.

The role requires a Bachelor's degree in Engineering or related discipline and 5+ years of hands-on experience in GMP environments. Onsite work in Thousand Oaks, CA, five days a week, with a competitive salary and benefits package.