Are you a detail-oriented individual with a passion for ensuring quality and compliance? Are you looking for a challenging role where you can apply your technical expertise and analytical skills? Look no further, Abbott is seeking a Validation Engineer to join our team!As a Validation Engineer at Abbott, you will play a crucial role in ensuring the safety, effectiveness, and regulatory compliance of our products. You will be responsible for developing and executing validation protocols, analyzing data, and providing recommendations for process improvements. Your contributions will directly impact the quality and reliability of our products, ultimately improving the lives of patients worldwide.To be successful in this role, you must have a Bachelor's degree in Engineering or a related field, along with 2-3 years of experience in validation or quality assurance. Strong communication and problem-solving skills are essential, as well as a working knowledge of FDA regulations and quality standards.If you are ready to take on a dynamic and rewarding role with a global leader in healthcare, we encourage you to apply for the Validation Engineer position at Abbott. Join us in our mission to help people live healthier and better lives.
- Develop and execute validation protocols for new and existing products in accordance with FDA regulations and quality standards
- Analyze data from validation studies and provide recommendations for process improvements
- Collaborate with cross-functional teams to ensure compliance with all relevant guidelines and standards
- Provide technical expertise and support for validation activities
- Conduct risk assessments and develop risk mitigation strategies
- Create and maintain validation documentation, including protocols, reports, and standard operating procedures
- Participate in design reviews and provide input on product design and development from a validation perspective
- Communicate validation findings and recommendations to relevant stakeholders
- Stay up-to-date on industry trends, regulations, and best practices related to validation and quality assurance
- Work with external vendors and suppliers to ensure their processes and products meet our validation requirements
- Act as a subject matter expert on validation during internal and external audits
- Train and mentor team members on validation procedures and best practices.
Bachelor's Degree In Engineering Or A Related Field
Minimum Of 3 Years Experience In Validation Within The Medical Device Or Pharmaceutical Industry
Strong Knowledge Of Regulatory Requirements, Including Fda And Iso Guidelines
Experience With Validation Protocols, Risk Assessments, And Statistical Analysis
Excellent Communication And Problem-Solving Skills, With The Ability To Work In A Fast-Paced And Team-Oriented Environment.
Documentation
Quality Assurance
Process Improvement
Data Analysis
Problem Solving
Test Planning
Technical Writing
Risk assessment
Regulatory compliance
Team collaboration
Software validation
Protocol Development
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Problem Solving
Time management
creativity
Critical thinking
Teamwork
Adaptability
According to JobzMall, the average salary range for a Validation Engineer in Columbus, OH, USA is between $72,000 and $110,000 per year. This can vary depending on factors such as experience, education, and the specific industry or company the engineer is working for.
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From removing the regular pain of finger sticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s blood donations to ensure a healthy supply, our purpose is to make the world a better place by bringing life-changing health technologies to the people who need them. That’s our commitment to helping you live your best life.

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