Veristainc4mo ago

CQV Engineer (New Grad)

Portland · Portlandmid

OtherCqv Engineer

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Quick Summary

Key Responsibilities

New or recent graduates are encouraged to apply Authoring, editing, and executing technical commissioning,

Technical Tools

OtherCqv Engineer

Description

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

~1 min read

→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

~2 min read

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

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

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For more information about our company, please visit us at Verista.com