Validation Specialist III – Diagnostics & Molecular

RXinsider LTD.

Madison (WI)

On-site

USD 61,000 - 123,000

Full time

14 days+
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Benefits offered by this job

Health coverage
Retirement savings plan with high-empl
Tuition reimbursement
FreeU education benefit
Career development opportunities

Job summary

Abbott in Madison, WI, is seeking a Validation Associate III to lead and participate in validation activities across computer systems, equipment, test methods, and cleaning processes. The role supports design transfers and ongoing process improvements within a GMP framework.

The position requires a life sciences degree (or related) with 3+ years of validation experience, strong documentation and Excel skills, and the ability to work cross-functionally. Travel up to 10% may be involved.

Qualifications

  • Bachelor’s degree in life sciences or related field required or an Associate’s degree with 2+ years of experience in lieu of a bachelor’s degree
  • 3+ years of validation experience in a relevant manufacturing setting
  • Demonstrated proficiency in molecular biology techniques and basic statistics

Responsibilities

  • Author validation plans, validation protocols, and validation summary reports for computer systems, processes and equipment
  • Execute validation or qualification protocols and document results
  • Prepare executed validation binders and supporting data
  • Review or approve documents prepared by team members
  • Support design transfer processes and continuous improvements projects

Skills

Teamwork
Documentation
Communication

Education

Bachelor’s degree in life sciences or related field
Associate’s degree in life sciences or related field

Tools

MS Excel
MS Word
Microsoft Office

Job description

Abbott in Madison, WI, is seeking a Validation Associate III to lead and participate in validation activities across computer systems, equipment, test methods, and cleaning processes. The role supports design transfers and ongoing process improvements within a GMP framework.

The position requires a life sciences degree (or related) with 3+ years of validation experience, strong documentation and Excel skills, and the ability to work cross-functionally. Travel up to 10% may be involved.

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