5782 - CQV Engineer / Validation Engineer

Verista; Scarborough (ME); On-site; USD 65,000 - 105,000; Full time

Job summary

Verista seeks a CQV Engineer in Scarborough, ME to support validation activities in a life sciences context. The role involves authoring technical documentation, executing testing, and ensuring compliance with GMP standards. Candidates must hold a STEM Bachelor's degree and have relevant experience, along with strong problem-solving skills.

Benefits

Competitive pay and performance-based incentives

Medical, Dental & Vision insurance

401(k) Retirement Plan with employer matching

Paid Time Off and Holidays

Tuition Reimbursement

Team Social Activities

Qualifications

• Bachelor’s degree in a STEM field is required.
• 3+ years leading CQV activities preferred.
• Experience in GMP regulated environment.

Responsibilities

• Authoring and executing validation documentation for equipment and processes.
• Running test scripts and documenting results.
• Maintaining comprehensive records for quality assurance.

Skills

Problem-solving

Critical thinking

Organizational skills

Attention to detail

Interpersonal skills

Communication

Education

Bachelor's Degree (STEM highly preferred)

Tools

Microsoft Office

Job description

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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
  
  

CQV Engineer / Validation Engineer Responsibilities

• Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software and processes as directed by the project leader
• Running test scripts and documenting results
• Adhering to 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
• Understanding capital equipment implementation and process knowledge
• Understanding validation documents, URS, IQ, OQ, PQ
  
  

Requirements

• Must be willing to work onsite in Scarborough, ME
• Bachelor’s Degree or equivalent required (STEM degree highly preferred)
• 3+ years of experience in leading CQV activities specific to Process Equipment 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
  
  

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

• Verista is an equal opportunity employer.
  
  

National (US) Range

$65,000—$104,439 USD

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

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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