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Manufacturing Engineer

  • Job reference: 930915
  • Location: Cork
  • Salary: Negotiable
  • Job type: Contract
  • Sector: Engineering, Manufacturing & Facilities, Life Sciences
  • Date posted: 08/05/2020

Orion Group Life Sciences have an exciting opportunity for a Manufacturing Engineer for our Multinational Medical Devices client based in the Cork area on an initial 12-month contract.


Job Purpose

This role supports manufacturing operations in the areas of process development, tool design, machine programming, machinery & equipment acquisition, manufacturing layout, continuous improvement and other duties associated with engineering support of production.

Main Responsibilities of the role
* Provides technical support in identifying continuous improvements to manufacturing operations and implementing new technologies including development of processes, researching current and emerging technologies and evaluating process quality, cost, capacity and capability alternatives.
* Supports the needs of manufacturing areas in terms of meeting the requirements for quality standards and compliant documentation, capacity, product availability and cost.
* Provides technical support regarding equipment design and development, testing of materials, preparation of specifications and operator instructions, process studies, investigations, root cause analysis, problem solving and report or presentation preparation.
* Performs assignments designed to continue the development of professional work knowledge and abilities requiring application of standard engineering techniques, procedures and criteria in carrying out a sequence of related engineering tasks, project management, statistical analysis and presentation of data and technical writing.
* Leads engineering projects that are less complex, either technically or with a small cross-functional team. Leads and participates in projects including developing and executing to the plan and schedule and meeting the goals and objectives of the project. Tracks costs, prepares status reports, conducts meetings, and documents and communicates progress to management.
* Leads and participates in investigations, develops plans and executes tasks to solve process problems including Nonconformances (NC), complaint investigations, audit observations and Corrective and Preventive Actions (CAPA).
* Provides day to day support and direction to production such as, but not limited to turning, milling, drilling, EDM, finishing, packaging etc. as required.
* Writes and executes engineering studies and process validation protocols and summary reports (Installation Qualification, Operation Qualification, Performance Qualification, Computer Software Validation and Test Method Validation).
* Identifies and implements process improvements for existing manufacturing processes utilizing appropriate engineering principles and standard strategies such as, Lean and Six Sigma principles.
* Performs gage design, measurement system analysis, and gage implementation as required. Is able to use various types of measuring instruments including, micrometers, calipers, comparators, tensile testers, coordinate measurement systems etc. to support engineering testing.
* Develops fixtures and designs tools and has the ability to express and implement ideas with tool designers.
* Supports new equipment acquisition efforts including user requirement specifications, machine selection, installation, validation, employee training, and other related equipment responsibilities as required.
* Develops and implements manufacturing and inspection procedures.

Desired Experience and Background of the successful candidate
* Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree.
* Demonstrates strong written, verbal and presentation skills.
* Demonstrates strong computer skills, such as the use of Microsoft Office, Minitab, and databases.
* Demonstrates strong organizational and project management skills and are results oriented.
* 2-4 years of experience in manufacturing and/or engineering is required.
* Previous experience working in a regulated industry, such as Medical Device is preferred.
* Six Sigma or Lean Sigma certification or 2 years of experience preferred.
* Must be willing to support global projects including some travel.
* Must be willing to support all production shifts.
* Participates in and understands compliance related activities pertaining to the job assignment including compliance with the Quality System Regulation (QSR), Standard Operating Procedures (SOP), and applicable Work Instructions.
* Follows all laws and policies as they apply to one's job and maintains the highest levels of professionalism, ethics and compliance at all times.
* Works in conditions that may be hot, cold, wet and/or noisy along with exposure to fumes, oil, coolants and other manufacturing related chemicals.

#medicaldevices #medical #device #13485 #multinational #product #implant #manufacturing #engineering

For more information on this role, call Daniel Ryan on +353868140295 or email Daniel.Ryan@orioneng.com for a completely confidential chat about this role and other opportunities using the reference number: 930915


Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

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