Posts Tagged ‘Quality Control’

Quality Engineer for Midlands

Tuesday, September 7th, 2010
Quality Engineer  - Complaints

Quality Engineer - Complaints

Our Medical Device Client based in the Midlands is seeking a

 Quality Engineer for a Complaints Coordinator job.

 

Essential Skills / Experience

 
• Engineering/Science qualification 
• 2/3 years of working within a Quality environment
• Excellent technical writing skills – essential
• Attention to detail and accuracy – essential
• Ability to work well under deadlines and pressure
• Problem solving skills for developing creative solutions and meeting objectives are required.
• Skills that enable coordination of data, including MS-Office (primarily PowerPoint, Word, MD Project, Outlook and Excel);
• Excellent analytical ability
• The ability to prioritize tasks and be able to manage several projects and tasks simultaneously; and the ability to interface with all levels of management.

 

Job Purpose

 
The successful candidate will act as the primary contact within the EMEA region for Field Actions associated within the EMEA region.  He/She will be responsible for ensuring activities associated with Field Actions are approved, communicated, written and delivered as appropriate.  This will include initiation of Field Actions, ensuring compliance to associated regulatory requirements, creation and completion of the necessary paperwork required to complete the Field Action.  The role will also involve multi-site collaboration with local Company offices in addition to Customer Services and Legal Manufacturers.  The candidate will be responsible for providing regular status reports to Management and Regulatory Authorities as required.

 

For more information on this role, or to apply, go to -

http://www.jackiebrownmedical.ie/jobs_ireland.php?url=jobs&page=2

Validating Quality Control

Thursday, February 4th, 2010
Validation Engineer Validating Medical Device Equipment

Validation Engineer Validating Medical Device Equipment

Validating Quality Control is essential for products being manufactured under extremely highly tolerances and to demanding Quality standards such as those found with medical device and pharmaceutical manufacture.

Validation is a quality control process that measures and tests against requirements that a system, product or service is achieving what it is required to do. For instance in manufacturing it is a process of zeroing equipment or plant to the exact parameters it must operate to, to produce product to an exact standard inorder to achieve a stated and fixed end result within fixed specifications outside of which it is not acceptable.

In essence it is  the process of fitness of purpose testing with the end user or other stake holders.

In many circumstances in manufacturing it can involve either computers, (hardware and software), equipment or an entire operating process or facility.

Validation in short can be explained by the question, “are you building the right thing?” and often requires reference to the Users Requirement Specifications or URS and the validation process can require a set of stringent protocols to achive completion referred to by the following terminology, IQ (Installation Qualification/OQ(Operational Qualification/Performance Qualification 

Opportunities  in Science jobs in Ireland today include positions for Validation Engineers, Validation Managers and Validation Document Control for a variety of industries and are readily found in high spec environments such as Biopharma, Pharmaceuticals, Semiconductors and Medical Device Manufacturing and are amongst some of the most highly paid science and engineering occupations availlable despite the current economic conditions.