Validation Technician Nutrition Manufacturing Casa Grande, AZ

JOB DESCRIPTION:

Validation Technician - Nutrition Manufacturing - Casa Grande AZ

We are seeking a detailoriented Validation Technician to support validation and change control activities across equipment systems utilities and processes in a regulated manufacturing environment. This role ensures that all systems meet defined requirements comply with cGMP standards and maintain auditready documentation.

Working at Abbott

At Abbott you can do work that matters grow and learn care for yourself and your family be your true self and live a full life. Youll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution
• Tuition reimbursement the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelors degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity working mothers female executives and scientists.

The Opportunity

This position works out of our Casa Grande Arizona location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands including Similac PediaSure Pedialyte Ensure and Glucerna to help them get the nutrients they need to live their healthiest lives.

Casa Grande AZ. is one of Abbotts leading nutrition manufacturing plants in the U.S. reflecting our commitment to innovation and excellence. But were more than just a company were a family. Working here youll be part of a family that works together to make a difference and enhance the lives of millions worldwide.

What Youll Work On

• Support execution and documentation of validation and change control activities in compliance with site procedures Abbott Nutrition policies and regulatory requirements (cGMP GDP).
• Assist with Design Qualification documentation and activities including System Impact Assessments (SIA) User Requirement Specifications (URS) and validation protocols and reports.
• Perform handson execution of validation protocols (IQ OQ PQ CSV) including data collection verification and proper documentation.
• Compile review and maintain validation documentation to ensure accuracy completeness traceability and adherence to Good Documentation Practices.
• Support change control activities including impact assessments documentation updates and validation tasks associated with equipment or process modifications.
• Assist with investigations and resolution of validation deviations discrepancies and data issues; escalate concerns appropriately.
• Maintain validation files logs and trackers to support compliance audits and inspection readiness.
• Collaborate with Engineering Quality Operations and IT teams to meet validation requirements and project timelines.
• Provide documentation and support during internal and external audits and inspections.
• Follow all site safety quality and documentation standards and perform additional duties as assigned.

What You Bring

• Strong attention to detail with the ability to accurately follow procedures and protocols in a regulated environment.
• Working knowledge of Good Documentation Practices (GDP) and basic understanding of cGMP principles.
• Ability to execute validation protocols and collect objective evidence under guidance.
• Skilled at identifying discrepancies or deviations and escalating appropriately.
• Organized methodical and able to maintain compliance auditready documentation.
• Effective communication skills and ability to work both independently and within crossfunctional teams.
• Proficiency in Microsoft Word Excel and Outlook.
• Flexibility to support changing priorities schedules and occasional offshift work.

Youll be accountable for meeting our compliance standards including FDA OSHA and Abbott policies and procedures.

Required Qualifications:

• Bachelors degree in Life Science Engineering or a closely related discipline.
• Up to 1 year of experience in Quality Validation Engineering or a related field within food manufacturing or similarly regulated industries (e.g. diagnostics medical devices pharmaceuticals).
• Strong understanding of Design Control GDP and cGMP.
• Experience with protocol writing execution and closure of validation activities.

In compliance with federal law all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Pre-Employment Inquiries and Citizenship U.S. Equal Employment Opportunity Commission ()

Apply Now

Learn more about our health and wellness benefits which provide the security to help you and your family live full lives:

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity and Military/Veteran friendly Employer committed to employee diversity.

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The base pay for this position is

In specific locations the pay range may vary from the range posted.

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