5741 - ISO 17025 Technical Writer / Quality Specialist

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

ISO 17025 Technical Writer / Quality Specialist:

This individual will be responsible for drafting, revising, and standardizing quality documentation to support the remediation of ISO/IEC 17025:2017 non-conformances. This role ensures clear, compliant, and audit-ready SOPs, work instructions, CAPA documentation, and quality records aligned with accreditation and regulatory expectations.  

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  Develop and revise SOPs, forms, and technical documentation related to ISO 17025 remediation activities.

  
  


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  Translate corrective action plans and audit findings into clear procedural updates.

  
  


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  Collaborate with subject matter experts to ensure technical accuracy and consistency.

  
  


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  Maintain document control in compliance with client internal quality systems.

  
  


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  Support CAPA documentation, effectiveness checks, and evidence gathering for accreditation readiness.

  
  


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  Ensure that all revised documents meet ISO 17025 formatting and content standards.

  
  

Requirements:

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  Bachelor’s degree in a scientific, technical, or quality-related discipline.

  
  


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  Experience writing technical or quality system documentation in a laboratory or regulated environment.

  
  


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  Working knowledge of ISO/IEC 17025:2017 and quality system remediation best practices.

  
  


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  Strong attention to detail, organization, and clarity in writing.

  
  


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  Familiarity with document control systems or electronic QMS platforms (preferred).

  
  


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  Demonstrated ability to generate high-quality project deliverables independently by required due dates.

  
  


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  Capacity to identify issues and proactively elevate to the project lead.

  
  


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  Advanced Microsoft WORD, EXCEL, and PowerPoint capabilities

  
  


• Minimum 2-5 years of role relevant experience.

This is a hybrid role with travel to site once per month in Baton Rouge, LA required.

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