2.0 Key Responsibilities and End Results: (Essential responsibilities include but are not limited to the following):
• Conduct first-off inspections for production start-ups.
• Conduct patrol inspections verifying attribute and variable data.
• Record data in log book/inspection files and SPC software.
• Label defective material accordingly to ensure positive identification.
• Retain defective samples for daily production review.
• Support rework/re-screen activities to ensure compliance to requirements and sign off relevant documentation effectively.
• Support the amendment of product specific documentation as part of the continuous improvement process.
• Support QE’s on new product introduction.
• Conduct OBA’s (Out of the Box Audits) when appropriate.
• Conduct label reconciliation requirements.
• Conduct any additional activities from a Quality perspective as deemed necessary by the primary Quality Engineer/Team Leader.
• Support all company safety and quality programs and initiatives.
• Ensure ongoing compliance with GMP in all practices, recording of events and processes.
• Ensure compliance with all learnings from all GMP training events.
• 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.
3.0 Job Specifications: The minimum education and experience required to perform this job competently.
• Leaving Certificate.
• Basic quality control concept understanding (desirable: level of service within a Quality control role), administration and record control experience.
• Understanding of Metrology desirable.
Skills/Attributes:
• Energetic, enthusiastic individual wanting to make a difference.
• Excellent initiative, decision-making and be able to work in a core team environment.
• Performance and results driven and excellent attention to detail
• Good oral & written communication skills.
• Possess strong analytical abilities.
• Intermediate level of computer skills.
4.0 Organization Linkages: List the titles of individuals and organizations with which this position has the most frequent and significant contact. Briefly describe the nature of those contacts.
Reports to Team Leader.
Operations and Managers.
Quality Team.
*If performing a Quality Inspector role for Pharmaceutical Assembly Product, Job Description WD Quality Inspector Pharmaceutical Assembly BY-JD-2019-0305 applies.
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.
Full-Time
Global manufacturing solutions provider for various industries
No salary listed
Entry, Junior
Company Historically Provides H1B Sponsorship
Kilkenny, Ireland
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Jabil provides manufacturing solutions across various industries, including healthcare, automotive, consumer electronics, and industrial sectors. The company offers end-to-end services, managing everything from product design and engineering to final assembly and distribution. This comprehensive approach helps clients streamline operations, cut costs, and speed up product launches. Jabil stands out from competitors by utilizing advanced analytics to enhance production processes and deliver better value. The goal of Jabil is to support leading brands in efficiently bringing their products to market while optimizing their manufacturing and supply chain operations.
Company Size
10,001+
Company Stage
IPO
Headquarters
Saint Petersburg, Florida
Founded
1966
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Health Insurance
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Remote Work Options
401(k) Retirement Plan
Paid Vacation
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