CQV Engineer (New Grad)

Verista, Inc.; Columbus (OH); In loco; USD 65.000 - 95.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive pay

Life Insurance

Disability Insurance

Tuition Reimbursement

Paid Time Off

Holidays

Sick Time

Parental Leave

Health Savings Account

Team Social Activities

Employee Referral Program

Descrizione del lavoro

Verista is seeking an experienced CQV professional to lead commissioning, qualification and validation activities for process equipment at our Columbus, OH site. You will develop testing strategies, author validation documents and ensure compliance with GMP standards while coordinating with project teams.

The role emphasizes collaborative problem solving, precise documentation, and adherence to project timelines in a fast-paced life sciences environment.

Competenze

• Bachelor’s degree required; STEM degree highly preferred.
• Experience leading CQV activities for Process Equipment.
• Proficiency with GMP and documentation practices.
• Willingness to work onsite in Columbus, OH.

Mansioni

• Author, edit and execute commissioning, qualification and validation documentation for equipment and systems as part of a project team.
• Develop and document testing strategies, test scripts and acceptance criteria.
• Review and document risk assessments and testing results.
• Maintain detailed qualification records and ensure alignment with project schedules.

Conoscenze

CQV leadership

Strong communication

Team collaboration

Problem solving

Attention to detail

GMP experience

Formazione

Bachelor’s Degree in STEM

Strumenti

Microsoft Word

Microsoft Excel

PowerPoint

Descrizione del lavoro

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
• 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

Requirements

• Must be willing to work onsite in Columbus, OH
• Bachelor’s Degree or equivalent required (STEM degree highly preferred)
• Demonstrated experience in leading CQV activities specific to Process Equipment
• Proficiency using PC and Microsoft Office tools
• Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
• Ability to work as part of a team
• Strong problem-solving and critical thinking skills
• Excellent organizational and time management skills
• Strong attention to detail
• 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
• Strong interpersonal skills and clear communication capabilities
• 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

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.
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 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