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Quality Engineer(24 Month Contract)

Title : Quality Engineer(24 Month Contract) profile
Sector : Manufacturing & Production
Engineering & Technical
Location : West Meath
Reference : CW121921
Contact : Tom Devaney
Office : Galway
Tel : 00353-91-758771
Email : tdevaney@careerwise.ie

Job Description

A Quality Engineer on a 24 Month Contract is required by CareerWise Recruitment for our Athlone based client. Qualified person to Level 8 Degree in a relevant Quality/Engineering/Science related discipline and preferably with 4-6 years relevant experience in a medical devices or similar regulated environment, with at least 3 years in a comparable role. Please contactTom Devaney for more information.

Role of this position

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
  • As part of process improvement projects, prepare the process validation protocols and work with the relevant process engineer in terms of execution of the validation and documentation of the resulting test report.
  • Lead deployment of root cause analysis tools and approaches through the organization with a specific focus on deviation resolutions.
  • Liaise with process engineers and other departments as relevant on the revalidation/introduction of new automation/tooling /processes/software/utilities /product to ensure that all aspects of validation are being covered
  • Risk Management - As part of a team co-ordinate the completion of Risk Management to include the use of tools such as Failure Modes Effect Analysis (FMEA), Fault Tree Analysis etc. to all product groups.
  • Suggest relevant changes to procedures and update to standard operating procedures as necessary.
  • Work with supervisor in terms of establishing gaps in the Project Validation Master Plans, creating schedules/timelines to address same and regularly reviewing the Master Validation Plan for adequacy
  • Provide quality engineering support to your functional area, helping to drive improvements, contributing to investigating root cause of quality issues and following through on corrective actions to prevent reoccurrence.
  • Liaise with cross functional team members, developing strong partnering relationships with these to establish inspection methods which ensure effective product acceptance actives.
  • Generate and understand of product construction, features and use at a competent level in order to make decision on product acceptance standards within the scope of your responsibility.
  • Support on-going communication through reports and information transfer as needed.
  • Develop and maintain analysis techniques and other quality control tools to aid in decision making.

JOB REQUIREMENTS

  • Qualified person to Level 8 Degree in a relevant Quality/Engineering/Science related discipline.
  • Preferably with 4-6 years relevant experience in a medical devices or similar regulated environment, with at least 3 years in a comparable role.
  • Dynamic team player and leader, with the ability to work effectively and proactively on cross-functional teams
  • Ability to be self-directed and to effectively interface with various levels and functions within the organization
  • Results driven and dynamic team player and can work effectively and proactively on cross-functional teams.
  • Knowledgeable in Quality Systems, validation standards, policies, procedures and methodologies. Knowledge, understanding and implementation of GAMP5 is an advantage.
  • Experienced with practical working knowledge of statistical data analysis and quality improvement tools and techniques.
  • Think critically and make sound decisions.
  • Focused on patient and customer and set high standards, in still operational excellence, and drive accountability.
  • Excellent written, documentation, and oral communication skills and are fluent in English, both written and spoken.
  • Excellent organizational skills and have the ability to prioritize and work effectively on multiple projects.
  • Good communication skills.

Please call Tom Devaney today for further information on 091-758771 or email: tdevaney@careerwise.ie

CareerWise Recruitment (In Search of Excellence)
Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the Medical Devices, Pharmaceuticals, Life Sciences, ICT, Engineering, Food and Agri sectors.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.

By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent.

 

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Careerwise Recruitment



Quality Engineer(24 Month Contract)

Title : Quality Engineer(24 Month Contract) profile
Sector : Manufacturing & Production
Engineering & Technical
Location : West Meath
Reference : CW121921
Contact : Tom Devaney
Office : Galway
Tel : 00353-91-758771
Email : tdevaney@careerwise.ie

Job Description

A Quality Engineer on a 24 Month Contract is required by CareerWise Recruitment for our Athlone based client. Qualified person to Level 8 Degree in a relevant Quality/Engineering/Science related discipline and preferably with 4-6 years relevant experience in a medical devices or similar regulated environment, with at least 3 years in a comparable role. Please contactTom Devaney for more information.

Role of this position

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
  • As part of process improvement projects, prepare the process validation protocols and work with the relevant process engineer in terms of execution of the validation and documentation of the resulting test report.
  • Lead deployment of root cause analysis tools and approaches through the organization with a specific focus on deviation resolutions.
  • Liaise with process engineers and other departments as relevant on the revalidation/introduction of new automation/tooling /processes/software/utilities /product to ensure that all aspects of validation are being covered
  • Risk Management - As part of a team co-ordinate the completion of Risk Management to include the use of tools such as Failure Modes Effect Analysis (FMEA), Fault Tree Analysis etc. to all product groups.
  • Suggest relevant changes to procedures and update to standard operating procedures as necessary.
  • Work with supervisor in terms of establishing gaps in the Project Validation Master Plans, creating schedules/timelines to address same and regularly reviewing the Master Validation Plan for adequacy
  • Provide quality engineering support to your functional area, helping to drive improvements, contributing to investigating root cause of quality issues and following through on corrective actions to prevent reoccurrence.
  • Liaise with cross functional team members, developing strong partnering relationships with these to establish inspection methods which ensure effective product acceptance actives.
  • Generate and understand of product construction, features and use at a competent level in order to make decision on product acceptance standards within the scope of your responsibility.
  • Support on-going communication through reports and information transfer as needed.
  • Develop and maintain analysis techniques and other quality control tools to aid in decision making.

JOB REQUIREMENTS

  • Qualified person to Level 8 Degree in a relevant Quality/Engineering/Science related discipline.
  • Preferably with 4-6 years relevant experience in a medical devices or similar regulated environment, with at least 3 years in a comparable role.
  • Dynamic team player and leader, with the ability to work effectively and proactively on cross-functional teams
  • Ability to be self-directed and to effectively interface with various levels and functions within the organization
  • Results driven and dynamic team player and can work effectively and proactively on cross-functional teams.
  • Knowledgeable in Quality Systems, validation standards, policies, procedures and methodologies. Knowledge, understanding and implementation of GAMP5 is an advantage.
  • Experienced with practical working knowledge of statistical data analysis and quality improvement tools and techniques.
  • Think critically and make sound decisions.
  • Focused on patient and customer and set high standards, in still operational excellence, and drive accountability.
  • Excellent written, documentation, and oral communication skills and are fluent in English, both written and spoken.
  • Excellent organizational skills and have the ability to prioritize and work effectively on multiple projects.
  • Good communication skills.

Please call Tom Devaney today for further information on 091-758771 or email: tdevaney@careerwise.ie

CareerWise Recruitment (In Search of Excellence)
Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the Medical Devices, Pharmaceuticals, Life Sciences, ICT, Engineering, Food and Agri sectors.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.

By applying for this position, you are consenting to allow CareerWise Recruitment to process and retain your data in accordance with our Privacy Policy, contained on our website for the purposes of providing career opportunities. CareerWise Recruitment accepts that you do not wish your personal data, including your CV, to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will always be respected. Please feel free to contact us if you have any queries or wish to withdraw or amend your consent.

 

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