5722 - Senior CQV Engineer / Senior Validation Engineer 2

Verista; Bloomington (IN); On-site; USD 80,000 - 128,000; Full time

Job summary

Verista seeks a Senior CQV Engineer in Bloomington, IN to execute commissioning and qualification activities. The ideal candidate will have extensive experience with automated inspection machines and a background in GMP and validation documentation, helping to drive innovation in the life sciences sector.

Benefits

Medical, Dental & Vision insurances

401(k) Retirement Plan (Employer Matching benefit)

Tuition Reimbursement

Paid Time Off (Rollover Option) and Holidays

Team Social Activities

Qualifications

• 5+ years experience leading CQV activities.
• Must have extensive experience with fully automated syringe inspection machines.
• General understanding of capital equipment implementation and process knowledge.

Responsibilities

• Execute commissioning activities and assist with qualification for automated inspection machines.
• Maintain document and execution trackers.
• Document impact and risk assessments as part of a team.

Skills

Problem-Solving

Critical Thinking

Interpersonal Skills

Communication Capabilities

Education

Bachelor’s Degree or equivalent

Tools

WORD

EXCEL

PowerPoint

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
  
  

Senior CQV Engineer Job Responsibilities

• Execute commissioning activities, edit/route applicable documents for approvals, and assist with qualification activities for the automated inspection machine (CAT2)
• Maintain document tracker, execution tracker, and list of open items
• Adhere with project schedule for all assigned activities
• Document impact and risk assessments as part of a team
• Develop, review, and execute testing documentation
  
  

Requirements

• Must be willing to work onsite in Bloomington, IN
• Bachelor’s Degree or equivalent required
• 5+ years experience in leading CQV activities
• Must have extensive experience with fully automated syringe inspection machines
• General understanding of capital equipment implementation and process knowledge
• Understanding validation documents, URS, IQ, OQ, PQ
• Ability to work independently and as part of a team
• Strong problem-solving and critical thinking skills
• GMP and Good Documentation Practice foundational knowledge
• 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
  
  

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

$80,465—$127,144 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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