Verista, Inc.
life science
ValidationEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Validation Engineer at Verista, Inc.. Skills: Commissioning, Qualification, Validation, CQV activities, Technical documentation. Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader. Running test scripts and documenting results”
What You'll Achieve.
empower informed decision-making; help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges; improve lives
Industry & Context.
problem-solving and critical thinking skills; Making recommendations for design or process modification based on test results
Must be willing to work onsite in Columbus, OH
What They're Looking For.
Must Have
Demonstrated experience in leading CQV activities specific to Process Equipment, Proficiency using PC and Microsoft Office tools, GMP and Good Documentation Practice, Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes), Basic skills with EXCEL and PowerPoint, Experience with and tolerance for high levels of challenge and change, Experience in GMP regulated environment, Proven attention to detail and organization in project work, Capable of working on assigned tasks without mentorship
Nice to Have
General understanding of capital equipment implementation and process knowledge, Understanding validation documents, URS, IQ, OQ, PQ
What You'll Do.
and executing technical commissioning
qualification and validation documentation for standard equipment/systems/ software
and processes as part of team as directed by the project leader
Running test scripts and documenting results
Adherence with project schedule for all assigned activities
detailed records qualification and validation
Documenting impact and risk assessments as part of a team
Completing user interface testing
software verification
and complete alarm testing on automated systems
and executing testing documentation
Making recommendations for design or process modification based on test results when executing test scripts
How You'll Work.
Team & Collaboration
as part of team as directed by the project leader; Documenting impact and risk assessments as part of a team; Ability to work as part of a team
Communication Scope
ability to communicate effectively with peers in clear, concise terms; clear communication capabilities
Process & Methodology
Adherence with project schedule for all assigned activities
Full Job Description
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 CQV Engineer Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader Running test scripts and documenting results Adherence with project schedule for all assigned activities Maintaining clear, detailed records qualification and validation Documenting impact and risk assessments as part of a team Completing user interface testing, software verification, and complete alarm testing on automated systems Developing, reviewing, and executing testing documentation Making recommendations for design or process modification based on test results when executing test scripts General understanding of capital equipment implementation and process knowledge Understanding validation documents, URS, IQ, OQ,
Applying for this Validation Engineer role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Greenhouse
- Create a Greenhouse profile before applying — it saves time across multiple applications.
- Upload your resume as a PDF; the parser handles it better than Word.
- Answer all knockout questions carefully — wrong answers auto-reject before a human sees you.
- Enable email notifications to track application status in real time.
ANONYMOUS · UNFILTERED
What do employees actually say about Verista, Inc.?
Real rants from real employees. Read before you apply.