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Employment Opportunities
 
We currently require the following personnel to support our rapidly growing business:
 
Regulatory Affairs Associate. (Temporary - Approx 6 Months) RAA-01
An opportunity has arisen within the Regulatory Affairs Department for a temporary Regulatory Affairs Associate, reporting to the Regulatory Affairs Manager.
Key responsibilities will be:
  • Participation in post-market surveillance activities
  • Preparation of post-market databases and reports
  • Preparation of associated regulatory submission documentation
    		•
    Key skills/experience required for the post will be:
  • Educated to degree level
  • Excellent attention to detail
  • Experience of Microsoft Word and Excel
    		•
    Regulatory experience within a medical device environment is desirable. The ideal candidate should have good communication skills, be a team player and have a meticulous approach to their work.
     
    Assistant Regulatory Affairs Manager. (Full-Time Permanent) ARA-01
    An opportunity has arisen within the Regulatory Affairs Department for an Assistant Regulatory Affairs Manager, reporting to the Regulatory Affairs Manager.
    Key responsibilities will be:
  • Production and review of Design Dossiers, Technical Files and Device Master Files
  • Preparation of regulatory submissions for global product registrations/approvals
  • Communicating with outside agencies/regulatory bodies
  • Update and review of IFUs, packaging, labelling and marketing literature
  • Oversee day to day actions of the RA department personnel based on RA Manager/departmental requirements
    		•
    Key skills/experience required for the post will be:
  • BSc degree or equivalent
  • Excellent attention to detail
  • Experience of Microsoft Word and Excel
  • Previous management experience
    		•
    Regulatory experience within a medical device environment is essential. The ideal candidate should have good communication skills, be a team player and have a meticulous approach to their work.
    This is a full-time permanent position.
     
    Temporary Quality Control Associates. (Temporary)
    Full Time (37 hours) and Part Time (24 hours)    		 QCA-01
    Opportunities have arisen within the Quality Control Department for temporary Quality Control Associates to work full time and part time hours.
    The full time post-holder will work 37 hours per week (Monday – Friday) to cover a period of maternity leave (approx 6 months).
    The part time post-holder will work 24 hours per week (Tuesday – Thursday) for a minimum period of 3 months.
    Key responsibilities will be:
  • Batch record review and release of product
  • Change control and issue of Company quality system documentation
  • Inspection and testing of raw materials
  • Verification of batch physical test data
    		•
    This is an ideal opportunity to expand on your work experience and gain valuable knowledge in a quality control environment.
    Previous quality control experience is essential. The ideal candidates should be computer literate, have excellent communication skills, be team-players and have good attention to detail. Some shift work may be necessary, therefore flexibility is essential.

    No Agencies Please.
     
    Quality Control Inspectors (Temporary) QCI-01
    As a result of both ongoing and new developments we now have vacancies for temporary Quality Control Inspectors for the following:
  • Visual inspection of in-process/finished products
  • Physical testing of products
  • Packaging & labeling verification
    		•
    Previous quality control experience is essential, preferably within a cleanroom environment. The ideal candidates should have good communication skills, be team-players and have excellent attention to detail. A flexible approach to working hours is required, as there may be some shift work involved.

    No Agencies Please.
     
    Manufacturing Administrator (Leeds) MAL-01
    An opportunity has arisen for a Manufacturing Administrator, based within the Heart Valve Division and reporting to the Operations Manager.
    Due to the nature of this position applicants should have an excellent telephone manner and a high level of customer commitment. The ability to work under pressure and a willingness to work as part of a team are prerequisites. Candidates must be computer literate with working knowledge of Microsoft Office packages, be able to demonstrate solid administration skills and have excellent attention to detail.
    Key duties will include:
  • Manufacturing process administration
  • Data entry of completed device history records using databases
  • Support of finished product packaging for Vascutek's manufactured products
  • Administrative support for the Heart Valve Division's health & safety committee
  • Support for goods inwards process
  • Responsibility for control and maintenance of manufacturing records, both hard copies and electronic records
    • Full training will be provided in all aspects of the position.
    This is a full-time permanent position.

    No Agencies Please.
     
    Production Operators (Temporary) POT-01
    This position will involve a variety of different manufacturing operations during the complete assembly of our products.
    Previous cleanroom and/or manufacturing experience would be advantageous but is not essential, however the ability to assemble and process components within stringent guidelines is essential. Sewing experience & skill would be highly beneficial. Manual dexterity and sewing tests will be given at interview. Support and training will be provided in all aspects of the position.
    The ideal candidates should be self motivated with a positive attitude and excellent communication skills. They will be team-players and have good attention to detail. The role involves working in a cleanroom environment and candidates must have a flexible attitude as overtime and shift work will be involved.
    To apply please contact us or forward your CV and a covering letter, indicating your current salary and the reasons why you feel you are suited to the post.
    No Agencies Please.
     
    To apply for any of the above positions, please send a full Curriculum Vitae, accompanied by a covering letter stating reference number and your current salary details to:

    HR Department, Vascutek Ltd., Newmains Avenue, Inchinnan, Renfrewshire PA4 9RR
    or e-mail your CV to vacancies@vascutek.com.