At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

• Generate and execute applicable validation documentation for facilities and injection moulding processes within the Quality Management System.

Key Responsibilities and End Results: (Essential responsibilities include but are not limited to the following):

• Generate applicable documentation to qualification and validation of facilities.
• Write the necessary validation protocols, & amendments of the Quality Management System ensuring compliance with the latest Regulatory Agencies (HPRA, FDA) directives / requirements within the Medical Device and Pharma Sector.
• Close liaison and networking with other departments, to provide and drive quality inputs and initiatives into the overall operational activities of the company.
• Development of validation projects.
• Support the implementation of Company Policies and GMP.
• Support all company safety and quality programs and initiatives.
• Experience in working with vendors.
• Ensure ongoing compliance with GMP in all practices, recording of events and processes.
• Ensure compliance with all learnings from all GMP training events.
• Perform and generate Risk Assessment documents for regulated processes within the scope of the QMS.
• Knowledge and use of LEAN 6 sigma tools for problem solution.
• Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position.

Job Specifications : The minimum education and experience required to perform this job competently.

• Degree in Engineering/Science discipline.
• 3 to 5 years’ experience in a Validation Quality Engineering role.
• Strong working knowledge of Validation Process and commissioning of facilities and equipment is an advantage.

Skills/Attributes:

• Strong working knowledge in the application of quality engineering tools and techniques with key emphasis on Eudralex, ISO13485, ISO14644, GAMP5 and FDA Pharma and medical devices regulations.
• Excellent organization, communication, computer, & presentation skills.
• Excellent initiative, decision-making and be able to work in a core team environment attaining resolutions.
Performance and Results driven.

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Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

Accessibility Accommodation

If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to [email protected] with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.

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