CQV Engineer (New Grad)

Veristainc; Portland (ME); On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

Medical, Dental & Vision insurances

401(k) Retirement Plan with Employer Matching

Paid Time Off and Holidays

Tuition Reimbursement

Team Social Activities

Job summary

Veristainc in Portland, ME is hiring for a crucial role involving technical documentation, validation, and testing processes in the life sciences sector. Candidates will work onsite and engage with team members on key qualification tasks. A Bachelor's degree in a STEM field is required, with an emphasis on organizational and critical thinking skills.

The role offers a competitive compensation package and extensive growth opportunities within a dynamic environment focused on empowerment and teamwork.

Qualifications

• Must be willing to work onsite in Portland, ME.
• GMP and Good Documentation Practice experience required.
• Demonstrated experience in CQV activities preferred.

Responsibilities

• Authoring and evaluating technical documentation.
• Running test scripts and documenting results.
• Maintaining detailed records for qualification and validation.

Skills

Ability to work as part of a team

Strong problem‑solving and critical thinking skills

Excellent organizational and time management skills

Strong interpersonal skills and clear communication

Education

Bachelor’s or equivalent STEM degree (Biomedical Engineer, Chemical Engineer, etc.)

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

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

Responsibilities

• New or recent graduates are encouraged to apply
• 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, PQ

Requirements

• Must be willing to work onsite in Portland, ME.
• Bachelor’s or equivalent STEM degree required (Biomedical Engineer, Chemical Engineer, etc.)
• Demonstrated experience in leading CQV activities specific to Process Equipment (internship experience preferred)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

Benefits

• 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

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