6190 - CQV Engineer / Validation Engineer

Verista, Inc. • Los Angeles, CA

5h • Onsite

About The Position

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
We empower and support our colleagues
We commit to client success at every turn
We have the courage to do the right thing
We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Requirements

• Bachelor’s degree in engineering, Life Sciences, or a related field
• 2-5+ years of relevant experience in validation within a regulated industry (e.g., pharma, biotech)
• Proven experience qualifying cleanroom facilities and manufacturing-scale process equipment
• Direct experience with centrifuges and filter presses at production scale (laboratory-only experience is not sufficient)
• Strong understanding of P&IDs and ability to interpret and verify in the field
• Demonstrated experience writing and executing validation protocols and authoring final reports
• Experience working in active construction and classified cleanroom environments
• Must be willing to be on-site, full-time in Los Angeles, CA
• Must be able (with 3-5 days notice) to work any shift, including holidays

Responsibilities

• Support qualification of cleanroom facilities and manufacturing-scale process equipment (vessels, centrifuges, filter presses, CIP skids)
• Execute validation protocols (IQ/OQ/PQ) and assist with final report authoring
• Perform construction walks and verify equipment installation against P&IDs and design documents
• Draft protocols, SOPs, and design documentation; support TOP and submittal reviews
• Maintain schedules, trackers, and documentation using systems such as DeltaV, Kneat, Veeva, Bluebeam, and MS365

Benefits

• Company-paid Life, Short-Term, and Long-Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level