Verista, Inc.

Verista, Inc.

CQV Engineer (New Grad)

Portland, Maine · Junior · Internship

Sponsorship not specifiedDetected 310 days ago
ExcelGMPCommunicationProblem SolvingCritical ThinkingTime ManagementMentoringMicrosoft Office

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odds of building a lasting career here

37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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About the role

  • 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 talented and dedicated professionals are committed to making an impact every day.

Responsibilities

  • Developing, reviewing, and executing testing documentation
  • Making recommendations for design or process modification based on test results when executing test scripts
  • Understanding validation documents, URS, IQ, OQ, PQ
  • We empower and support our colleagues

Requirements

  • Bachelor's or equivalent STEM degree required (Biomedical Engineer, Chemical Engineer, etc.)
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • 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

Nice to have

  • Demonstrated experience in leading CQV activities specific to Process Equipment (internship experience preferred)
  • Competitive pay plus performance-based incentive programs

Benefits

  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • Tuition Reimbursement
  • Paid Parental Leave and Bereavement

Company info

  • 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.
  • 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
  • Documenting impact and risk assessments as part of a team

This listing is sourced directly from Verista, Inc.'s careers page and normalized into a canonical job model.