QUALITY ENGINEER
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Job Reference Number |
14076673 |
Client ID: |
RI/753A |
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Posted On: |
Aug 26 2009 |
Location: |
MIDLANDS, LONGFORD |
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Job Type: |
Permanent
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Salary: |
SEE DESCRIPTION |
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Quality Engineer
My clients site in the midlands is expanding they currently are recruiting a Quality Engineer to Provide Quality Engineering support to Manufacturing, Testing and Support activities across the site.Plan and direct activities concerned with development, application, and maintenance of quality standards for site processes.Act as key Quality contact supporting Genesis Manufacturing workstream and other process improvements across the site.
RESPONSIBILITIES:
· Co-ordinate the execution of the site FDA-readiness action plan(s) via project-management leadership and interaction with all functional areas.
· Assist in identification of process / system improvements across the site, develop and execute plans to address same.
· Provide Quality Engineering support (problem solving, trouble shooting, FMEA, improvement initiatives) to all functions across the site.
· Provide quality leadership to key site initiatives e.g. 5S, Near Miss Program, CIPs etc.
· Lead problem solving and driving continuous improvements by analysis of quality data.
· Support all areas in identification and implementation of effective CAPAs.
· Support FDA-readiness training and awareness activities.
· Liaise with area owners to identify Quality system risks and co-ordinate improvement plans.
· Demonstrate an understanding of the application of the Quality Policy through daily activities. Maintain vigilance to ensure adherence to the Quality Policy and system procedures by promptly reporting noncompliance issues to management.
· Bring potential product / process Quality issues to the attention of Quality Management.
· Conduct business in a manner that will protect human health, safety and the environment by complying with all applicable EHS laws, as well as the Company Global & Technical Standards.
Requirements
Third level qualification in a Biomedical/Scientific/Quality/Engineering discipline with 2years in Quality, Technical, Regulatory or Manufacturing areas within the pharmaceutical or devices industry
·Knowledge of Quality Engineering Tools and Techniques (e.g. Lean / Six Sigma, FMEA) is a requirement for this role.
· Work collaboratively with sister sites, relevant Division-level functions and site functional leaders.
· Ability to assess and translate quality system requirements and improvement opportunities into actionable plans.
· Working within a highly regulated manufacturing environment with strong project management skills as this provides a good foundation for this job function.
· The ability to influence and work co-operatively and effectively with others to establish and maintain good working relationships.
· Excellent presentation skills.
· The highest level of integrity in the successful completion of your work.
· Advanced leadership skills in order to build and develop an effective team by providing clear direction and define priorities.
· Proven problem-solving skills and project management skills.
· Self Starter who can drive for results and meet or beat deadlines.
· Excellent communication skills.
Salary and benefits: Salary will depend on qualification and experience and my client pays very competitively within the market. Excellent benefits such as Health Insurance, Pension, Life Assurance, Educational Assistance and more are also in place for the successful applicant.
We have worked with this client for over four and a half years to great success and have remained one of their leading suppliers of staff during this time. We are in a position to provide additional company information, cv & interview preparation where all our candidates are met prior to their first formal meeting with our client. In a climate that has changed recently from a candidate's market place to a client's market place, Ormonde Recruitment places enormous value on our interview preparation & has proven to date that this interview preparation could place you ahead of other applicants applying for the same role.
Contact & Confidentiality
Please forward your cv in strictest confidence to Aoife at Ormonde Recruitment Ltd through the link provided or call 056-7786111 if you would like to discuss further options about this or other employment opportunities.
Ormonde Recruitment is a professional organization where all CV's will be kept confidential and will not be submitted to any potential employer without your prior knowledge, discussion & consent.
Should you wish to view other suitable roles which may match your skillset and experience more accurately, please visit our website for a listing of all vacancies within the medical device/pharmaceutical and other industry sectors including Operations & Manufacturing, Quality, Technical & Engineering, Supply Chain, IT, HR, Health & Safety, Finance, Administration & Multi-Lingual.