6250 - CQV Engineer / Validation Engineer
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 technical discipline
- 3+ years of CQV/validation experience within a GMP-regulated pharmaceutical or biotechnology manufacturing environment
- Demonstrated experience executing temperature mapping studies and supporting qualification of controlled temperature units, equipment, utilities, or facilities
- Proven ability to work independently with minimal oversight, managing validation activities, documentation, and protocol execution from planning through completion
- Strong knowledge of cGMP regulations, validation lifecycle practices (IQ/OQ/PQ), and documentation standards, with effective technical writing and problem-solving skills
- Ability to be on-site, full-time, in Kansas City, MO
Responsibilities
- Create and perform temperature mapping studies for controlled temperature units (CTUs), warehouses, stability chambers, cold rooms, incubators, and storage areas to ensure compliance with GMP and regulatory requirements
- Develop and execute commissioning and qualification protocols (IQ/OQ/PQ) for pharmaceutical manufacturing equipment, utilities, and facilities
- Author and maintain validation lifecycle documentation including URS, risk assessments, traceability matrices, and validation summary reports
- Coordinate qualification and validation activities with engineering, quality, manufacturing, and external vendors to support system installations and upgrades
- Support deviation investigations, change control, and CAPA activities related to validated systems and qualification activities
- Ensure all validation and qualification work is performed in compliance with cGMP, regulatory guidelines, and company validation standards
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
