5660 - CQV Engineer / Validation Engineer

Verista; Bloomington (IN); On-site; USD 70,000 - 119,000; Full time

Job summary

An established industry player is seeking a CQV Engineer to join their innovative team in Bloomington. This role involves authoring and executing essential validation documentation, running critical test scripts, and ensuring compliance with GMP standards. The ideal candidate will possess a Bachelor’s Degree and 1-4 years of relevant experience, along with proficiency in Trackwise and Microsoft Office tools. This position offers the opportunity to work collaboratively in a dynamic environment, contributing to vital projects that enhance healthcare solutions. If you are detail-oriented and passionate about making a difference in life sciences, this is the perfect opportunity for you.

Qualifications

• 1-4 years of experience leading CQV activities specific to Process Equipment.
• Experience in GMP regulated environments and ability to work independently.

Responsibilities

• Author and execute technical commissioning and validation documentation.
• Run test scripts, document results, and maintain clear records.
• Complete user interface testing and recommend design modifications.

Skills

CQV activities

Trackwise/QMS software

Microsoft Office tools

Effective communication

Problem-solving skills

Attention to detail

Education

Bachelor’s Degree

Tools

Trackwise

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

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Description

Verista’s team of 500 experts collaborates with the world’s most recognizable brands in the life sciences industry to address their business needs. Our mission is to empower growth and innovation within the scientific community, helping researchers, organizations, and companies solve pressing healthcare challenges. We provide innovative solutions and services that support informed decision-making, backed by significant investments in our people and capabilities.

Our growth is driven by world-class professionals who thrive in a team environment and share our mission to improve lives through life sciences. Our dedicated team is committed to making an impact every day.

Company Culture & 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 promote an inclusive environment where colleagues feel respected, engaged, and challenged.
• We continuously acquire new skills and learn from experiences to enhance our collective expertise.

CQV Engineer Responsibilities

• Author, edit, and execute technical commissioning, qualification, and validation documentation for equipment, systems, software, and processes as directed by the project leader.
• Run test scripts and document results.
• Adhere to project schedules for all assigned activities.
• Maintain clear, detailed records of qualification and validation activities.
• Document impact and risk assessments as part of a team.
• Complete user interface testing, software verification, and alarm testing on automated systems.
• Develop, review, and execute testing documentation.
• Recommend design or process modifications based on test results.
• Understand capital equipment implementation and process knowledge.
• Familiarity with validation documents such as URS, IQ, OQ, PQ.

Requirements

• Willing to work onsite in Bloomington, IN.
• Bachelor’s Degree or equivalent.
• 1-4 years of experience leading CQV activities specific to Process Equipment.
• Experience with Trackwise/QMS software.
• Proficiency with PC and Microsoft Office tools.
• Effective communication skills and outgoing personality.
• Ability to work collaboratively in a team.
• Strong problem-solving, organizational, and time management skills.
• Attention to detail and experience with GMP and Good Documentation Practices.
• Intermediate skills with Word; basic skills with Excel and PowerPoint.
• Experience in GMP regulated environments and ability to work independently.

Note: Salary range for US candidates is $70,491—$118,941 USD, dependent on various factors. Verista is an equal opportunity employer.