Job Description

Locations

• Ireland, Cork

Skills Required

• regulated environmentintermediate
• medical device industry is an advantageintermediate

Required Qualifications

• Holds (or is undertaking) cert/diploma/trade in related discipline or has minimum of 2 years additive manufacturing production experience in a regulated environment. (experience, 2 years)
• Holds (or is undertaking) cert/diploma/trade in related discipline or has minimum of 2 years additive manufacturing production experience in a regulated environment. (experience, 2 years)
• Experience in the medical device industry is an advantage. (experience)
• Experience in the medical device industry is an advantage. (experience)
• Computer literacy. (experience)
• Computer literacy. (experience)
• Demonstrated Mechanical/Technical Aptitude. (experience)
• Demonstrated Mechanical/Technical Aptitude. (experience)
• Strong communication skills. (experience)
• Strong communication skills. (experience)
• Ability to work on own initiative as part of a team in a fast paced, results oriented environment. (experience)
• Ability to work on own initiative as part of a team in a fast paced, results oriented environment. (experience)
• Proven problem solving skills and hands on approach. (experience)
• Proven problem solving skills and hands on approach. (experience)
• Experience of working in regulated GMP based machine floor environment required. (experience)
• Experience of working in regulated GMP based machine floor environment required. (experience)
• Capable of working as part of a multi-disciplined team. (experience)
• Capable of working as part of a multi-disciplined team. (experience)

Responsibilities

• Support AO project teams with 3D print machine build support and relevant post-production requirements. Co-ordinate builds and relevant post-production requirements in parallel with Operations support and report to AO project teams and relevant AO Technicians.
• Support AO project teams with 3D print machine build support and relevant post-production requirements. Co-ordinate builds and relevant post-production requirements in parallel with Operations support and report to AO project teams and relevant AO Technicians.
• Perform all necessary laboratory and Product Development testing and supply data required for FDA submissions. Equipment will include metallographic, optical microscopy, chemical and physical analysis, dimensional measurement, First Article Inspection etc. of metals, polymers etc. as required.
• Perform all necessary laboratory and Product Development testing and supply data required for FDA submissions. Equipment will include metallographic, optical microscopy, chemical and physical analysis, dimensional measurement, First Article Inspection etc. of metals, polymers etc. as required.
• Support DOEs, capability studies, MSAs, Technical support e.g. workmanship standards, product quality issue resolution, quality control support, engineering support.
• Support DOEs, capability studies, MSAs, Technical support e.g. workmanship standards, product quality issue resolution, quality control support, engineering support.
• Work closely with the Quality Department to ensure all documentation associated with validation and new product introduction in a regulated environment is accurate, executed in the correct sequence and completed in a timely manner.
• Work closely with the Quality Department to ensure all documentation associated with validation and new product introduction in a regulated environment is accurate, executed in the correct sequence and completed in a timely manner.
• Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
• Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
• Provide training for manufacturing team members.
• Provide training for manufacturing team members.
• Ensure adherence to GMP and safety procedures.
• Ensure adherence to GMP and safety procedures.
• All other duties as assigned.

Benefits

• general: Ireland: €17.26 - €28.60 EUR Hourly
• general: At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.
• general: If you’d like to learn more about the salary or the benefits associated with this role, your recruiter will be happy to walk you through the details as you progress through the hiring process.

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