6201- CQV Engineer / Validation Engineer at Verista in Muskegon, MI

Summary: Verista is a company that partners with leading brands in the life sciences sector to address critical healthcare challenges. They are seeking a CQV Engineer to author and execute validation documentation, run test scripts, and maintain detailed records as part of a team, ensuring adherence to project schedules and quality standards. Responsibilities: - 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 Required Qualifications: - Must be able to work onsite in Muskegon, MI - Bachelor's Degree or equivalent required (STEM degree highly preferred- new grads considered) - Exposure to Commissioning, Qualification and Validation concepts in GMP regulated environments - 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 Required Skills: Commissioning, Qualification, Validation Important Skills: GMP knowledge, Microsoft Office Nice-to-Have Skills: Problem-solving, Critical thinking, Attention to detail, Teamwork, Communication skills Benefits: 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