Skip to main content

Verista, Inc.

CQV/Process Engineer (New Grad)

Kalamazoo, Michigan, United States

Location
Kalamazoo, Michigan, United States
Work
Not stated
Employment
Not stated
Level
Not stated
Function
Engineering
Pay
Not stated
Posted
21 months ago

About the role

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/Process Engineer Responsibilities

CQV Engineers execute commissioning, qualification and validation projects involving new

or modified systems/equipment, processes, procedures, products, facilities, and utilities. In this role, validation

engineers support the validation and change lifecycles for client’s systems in pharmaceutical and medical device

manufacturing, laboratory, IT, and packaging operations to meet timeline, budget, quality, regulatory compliance,

and client expectations.

Process Engineers support conceptual and detailed design, support in process scale-up, product development, process validation, and implementation of operational improvements that resolve manufacturing process investigations in pharmaceutical manufacturing environments. In this role, you may work in concert with the client or as part of a Verista team tasked in determining the root cause of manufacturing investigations or in designing/executing experiments and evaluating data in support of improvement and investigations. Additionally, engineers write technical reports in support of manufacturing process changes, optimizations, and regulatory filings (where required).

This is an entry level role. College graduates are encouraged to apply. We are looking for smart, hardworking team players to grow professionally into this role at our client site in Kalamazoo, MI.

Requirements

  • Bachelor’s degree in chemical, biomedical/biochemical engineering, biological/chemical sciences or equivalent required
  • Must live in or relocate to the Kalamazoo MI area
  • 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
  • Ability to think critically and demonstrate troubleshooting and problem-solving skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • Possess excellent interpersonal, verbal, and written communication skills.
  • GxP and Good Documentation Practice training (may be completed at onboarding)
  • Process training (may be completed at onboarding)
  • 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

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

Source

Posted by Verista, Inc. on their own hiring page, job-boards.greenhouse.io. OptiTalent shows it as published, read 07 Nov 2026 05:12 UTC; the original is the reference.

View the original ad ↗

More at Verista, Inc.

  • Verista, Inc. · Finance, United States +1

    Remote$75K – $85K a yearFinance

    Responsible for end-to-end project accounting activities, including billing, collections, cash application, expense/vendor processing, and financial reporting for assigned accounts. Ensures compliance with A/P and A/R controls while collaborating cross-functionally with…

  • Verista, Inc. · Indianapolis, Indiana, United States

    $101.9K – $129K a yearEngineering

    We are seeking a Product Reliability Engineer to support the evaluation, analysis, and improvement of mechanical and electrical product designs. The ideal candidate will have a multidisciplinary engineering background with experience identifying potential product failure modes,…

  • Verista, Inc. · King of Prussia, United States

    RemoteSenior$70.5K – $118.1K a yearHealthcare

    We are seeking an experienced Computer System Assurance (CSA) Consultant to support GxP compliance activities across Pharmacovigilance (PV), Clinical, and Regulatory Affairs systems. This role will work closely with Quality, IT, and business stakeholders to ensure systems are…

  • Verista, Inc. · Cambridge, Massachusetts, United States

    Senior$90K – $136.2K a yearOperations

    Lead business analysis for an AI-enabled CMC regulatory authoring technology implementation; Translate CMC regulatory-authoring workflows into business, functional, data, integration, security, and non-functional requirements; Support the full SDLC, including discovery,…