Back to jobs
New

6498 - Senior CQV Engineer / Senior Validation Engineer

Wichita, KS

Description

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

Senior Validation Engineer Responsibilities:

  • Lead and/or support the execution of CQV activities for facilities, utilities, manufacturing equipment, laboratory systems, and computerized systems within GxP-regulated environments.
  • Author, review, and execute CQV documentation, including URS, risk assessments, qualification plans, protocols, test scripts, IQ/OQ/PQ documentation, commissioning documents, deviations, and validation/qualification summary reports.
  • Develop and execute qualification and testing activities, including IQ/OQ/PQ, functional testing, system walkdowns, field verification, punch-list management, and acceptance testing.
  • Coordinate and perform hands-on field execution, ensuring protocols are followed, test results are properly documented, and discrepancies are identified, investigated, and resolved.
  • Work with Engineering, Quality, Operations, Automation, and vendors to coordinate commissioning and qualification schedules, test execution, system readiness, and project deliverables.
  • Review engineering and vendor documentation, drawings, specifications, manuals, and test records to support CQV planning and execution.
  • Ensure CQV deliverables and execution activities comply with cGMP, GAMP 5, ASTM E2500, data integrity principles, and applicable regulatory requirements.
  • Manage and support deviations, discrepancies, change controls, and corrective actions associated with commissioning and qualification activities.
  • Maintain accurate documentation and ensure all executed records meet Good Documentation Practices (GDP) and client quality requirements.
  • Provide technical guidance and mentorship to junior CQV engineers and support the development of standardized CQV processes and templates.
  • Communicate project status, risks, issues, and deliverable progress to project and functional leadership.
  • Support multiple projects and priorities while maintaining quality, schedule, and execution commitments.

Job Requirements:

  • Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
  • 5+ years of hands-on CQV experience within pharmaceutical, biotechnology, medical device, or other regulated life sciences environments.
  • Demonstrated experience with both authoring and field execution of CQV/qualification documentation.
  • Strong experience developing and executing IQ/OQ/PQ protocols, commissioning documentation, test scripts, and qualification reports.
  • Experience with facilities, utilities, manufacturing equipment, laboratory systems, and/or computerized systems.
  • Strong understanding of cGMP requirements and the equipment/system qualification lifecycle.
  • Experience with deviation management, change control, punch-list management, and resolution of qualification issues.
  • Strong technical writing, documentation, organizational, and problem-solving skills.
  • Experience leading CQV activities or workstreams within large pharmaceutical or biotechnology capital projects.
  • Experience with GAMP 5, ASTM E2500, risk-based qualification approaches, and data integrity/ALCOA+ principles.
  • Experience working with engineering drawings, P&IDs, equipment specifications, and vendor documentation.

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range

$78,925 - $122,603 USD

Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • 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

Verista collects and processes personal data in accordance with applicable data protection laws.  If you are a California Job Applicant, see the privacy notice for further details. 

For more information about our company, please visit us at Verista.com

Apply for this job

*

indicates a required field

Resume/CV*

Accepted file types: pdf, doc, docx, txt, rtf

Education

Select...
Select...
Select...

Current residential street address (e.g. 1600 Pennsylvania Ave NW)

Please enter the city where you currently reside.

Select...

State in which you currently reside.

What are your specific areas of expertise?

Select...

Enter number of years of experience within the Life Sciences Industry, regardless of role.

Enter your number of years of role specific experience.

List any certifications your hold?

Select...
Select...

Traveling to support client needs are an expectation of Verista Resources.  Are you open to at least 50% travel?

Select...

Can you meet the travel and on-site requirements defined for this role?

Select...

Sponsorship question

Select...
Select...

U.S. Standard Demographic Questions

We invite applicants to share their demographic background. If you choose to complete this survey, your responses may be used to identify areas of improvement in our hiring process.
Select...
Select...
Select...
Select...
Select...
Select...

Voluntary Self-Identification

For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiring process or thereafter. Any information that you do provide will be recorded and maintained in a confidential file.

As set forth in Verista, Inc.’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.

Select...
Select...
Race & Ethnicity Definitions

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection. As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measure the effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categories is as follows:

A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.

A "recently separated veteran" means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.

An "active duty wartime or campaign badge veteran" means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.

An "Armed forces service medal veteran" means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.

Select...

Voluntary Self-Identification of Disability

Form CC-305
Page 1 of 1
OMB Control Number 1250-0005
Expires 07/31/2029

Why are you being asked to complete this form?

We are a federal contractor or subcontractor. The law requires us to provide equal employment opportunity to qualified people with disabilities. We have a goal of having at least 7% of our workers as people with disabilities. The law says we must measure our progress towards this goal. To do this, we must ask applicants and employees if they have a disability or have ever had one. People can become disabled, so we need to ask this question at least every five years.

Completing this form is voluntary, and we hope that you will choose to do so. Your answer is confidential. No one who makes hiring decisions will see it. Your decision to complete the form and your answer will not harm you in any way. If you want to learn more about the law or this form, visit the U.S. Department of Labor’s Office of Federal Contract Compliance Programs (OFCCP) website at www.dol.gov/ofccp.

How do you know if you have a disability?

A disability is a condition that substantially limits one or more of your “major life activities.” If you have or have ever had such a condition, you are a person with a disability. Disabilities include, but are not limited to:

  • Alcohol or other substance use disorder (not currently using drugs illegally)
  • Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS
  • Blind or low vision
  • Cancer (past or present)
  • Cardiovascular or heart disease
  • Celiac disease
  • Cerebral palsy
  • Deaf or serious difficulty hearing
  • Diabetes
  • Disfigurement, for example, disfigurement caused by burns, wounds, accidents, or congenital disorders
  • Epilepsy or other seizure disorder
  • Gastrointestinal disorders, for example, Crohn's Disease, irritable bowel syndrome
  • Intellectual or developmental disability
  • Mental health conditions, for example, depression, bipolar disorder, anxiety disorder, schizophrenia, PTSD
  • Missing limbs or partially missing limbs
  • Mobility impairment, benefiting from the use of a wheelchair, scooter, walker, leg brace(s) and/or other supports
  • Nervous system condition, for example, migraine headaches, Parkinson’s disease, multiple sclerosis (MS)
  • Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities
  • Partial or complete paralysis (any cause)
  • Pulmonary or respiratory conditions, for example, tuberculosis, asthma, emphysema
  • Short stature (dwarfism)
  • Traumatic brain injury
Select...

PUBLIC BURDEN STATEMENT: According to the Paperwork Reduction Act of 1995 no persons are required to respond to a collection of information unless such collection displays a valid OMB control number. This survey should take about 5 minutes to complete.