Posts Tagged ‘ISO’

QA Officer – (Medical Device) Oxfordshire

Tuesday, May 31st, 2011

Our client is a world leading Medical Device Organisation who is involved in the development of various medical devices & diagnostic products. They are currently looking for two QA Officers at different levels to join their Quality & Regulatory Team based from their site in Oxfordshire.

Responsibilities:

As a QA Officer (Medical Devices) you will be responsible for:

  • Assisting with the development of process & procedures on site
  • Review of quality documentation (ISO 13485) and device history records (DHRs) including approval/rejection of DHRs prior to release to sales & distribution
  • Provide support during internal and customer audits when required.

The senior of the two roles will also lead members of the quality team in absence of the team leader.

This is an outstanding opportunity to work with a leading name in the Medical Device industry. In return they offer an attractive salary and excellent benefits.

Qualification and Experience:

To be considered for this role, you will have demonstrated experience gained in a quality function including knowledge of ISO 13485 gained within the medical device, diagnostic or a related technology sector.

Apply now:

For more information or to apply for this QA Officer – Medical devices position.  Please contact Andrew Bolton on 01438 723 500 or abolton@ckscience.co.uk. Please quote reference ST22052 in all correspondence.

                                                   Click here to apply on line:

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Quality Manager Job – Scotland

Monday, May 9th, 2011

Our client a world-leading manufacturer of diagnostic reagents are looking for a Quality Manager to join their team in Scotland.

Responsibilities:

As Quality Manager you will be responsible for the management of quality management systems and procedures ensuring all products meet regulatory (ISO) and GMP compliance and customer specifications including liaising with relevant external and regulatory bodies.

Other responsibilities include:

  • Ensuring that procedure and practice implemented within supplier quality are consistent with best practice and comply with the necessary Quality and Regulatory requirements.
  • Being responsible for agreeing the appropriateness of all associated CAPA plans
  • Manage QA processes for incoming material with appropriate documentation and QMS
  • Manage effective batch review and release Process
  • Manage effective compliance by responding and implementing corrective actions post-audit (FDA) and encompassing both systems and processes.

 

Requirements:

The ideal candidate for this Quality Manager position will have quality assurance experience in the diagnostics or related industries.

This position also demands a working knowledge of quality assurance systems and the ability to represent the company on a professional level during on-site assessments at suppliers. Experience in the quality auditing systems at manufacturing facilities is also essential.

Apply now

For more information or to apply for this Quality Manager position, please contact Carrie-Ann Bell on 0191 384 8905 or email cbell@ckscience.co.uk. Please quote reference DH21856 in all correspondence.

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Quality Assurance (QA) Specialist Job – Berkshire, UK

Tuesday, January 11th, 2011

We are currently recruiting for a QA Specialist to join a Global Pharma company based in Berkshire in a brand new role to provide QA Support for Pharmaceutical products within their Medical Division.

We are looking for someone that is experienced in the following:

  • Developing and managing QMS
  • The management of complaint handling of both imported and UK manufactured products for UK markets
  • The development and implementation of Change Control systems
  • The management of non-conformance management processes (including ER, CAPA & SCARs)
  • The ability to conduct supplier audits and create / review technical agreements.

The ideal candidate for this QA Specialist position will have gained experience of QA within the Pharmaceutical or Medical Device industry and will be experienced with GDP and GMP. An understanding and preferably training in ISO and FDA/MHRA regulatory requirements is also required.

This QA Specialist role will involve travel to suppliers and occasional trips to European sites.

 

Apply Now

For more information or to apply for this QA Specialist position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST21098 in all correspondence.

 

Alternatively, click here to apply for this QA Specialist position online now.

 

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QA Auditor Job – Northern Ireland

Friday, January 7th, 2011

Our client is a specialist in implementing quality systems to businesses UK wide.  They have a requirement for a QA Auditor specialising in ISO 27001 to work for their client base throughout Northern Ireland

In your role as QA Auditor, you will conduct audits both desk based or on site, provide reports and support and provide advice in helping businesses to develop their quality systems.  You must be qualified to auditor status in ISO 27001, preferably to lead auditor level and possess a proven track record in auditing to ISO standards.

 

Apply Now

For more information, or to apply for this QA Auditor position, please contact Barney Smith at CK Science on 0191 384 8905 or email bsmith@ckscience.co.uk.  Please quote reference DH21065 in all correspondence.

Auditor Job (Food, Quality, Safety) – Home-based, UK

Tuesday, December 14th, 2010

Our client, a internationally leading Food & Consumer Goods Auditing organisation, are currently looking for an Auditor to join their growing team who service clients across the Food, Consumer, Cosmetic, Packaging and other industries. This is a home based position, with flexibility on location within the UK.

Working as an Auditor, you will be responsible for providing a consultancy based service to clients within the Food industry surrounding Quality & Safety across site.

Your duties will include auditing of Development and Manufacturing facilities in line with quality standards & food safety management systems (ISO, HACCP, BRC); providing guidance & expertise surrounding potential issues, validation & verification protocols and improvement programme’s on site as well as providing analysis of findings following the audit to be presented to the client in an audit report.

This is an outstanding opportunity to join the Food division of an Auditing Consultancy that continues to experience success globally. In return they offer an attractive salary and benefits package.

To be considered for this role, you will have a degree in a related Scientific, Engineering or Business discipline (or equivalent) and proven practical external and/or internal auditing experience gained in the Food Manufacturing Industry including knowledge of ISO, BRC and HACCP quality standards as well as Food Safety Management Systems.

 

Apply Now

For more information, or to apply for this Auditor job, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST21002 in all correspondence.

 

Alternatively, click here to apply for this Auditor position online now.

Regulatory Affairs Officer (Chemical) London, UK

Tuesday, August 24th, 2010

Our client, a world leading Chemical Distributor, are currently looking for a Regulatory Affairs Officer to join their UK flag ship facilities based in London, UK.

Working as a Regulatory Affairs Officer, you will be responsible for providing regulatory support to all departments on site including designing and outlining regulatory procedures as well as performing regulatory checks and auditing of all products (ISO 9001, ISO 14001, OHSAS 18001, GHP,REACH) and packaging (CLP) in line with industry quality standards. Your duties will also see you working closely with suppliers and customers to ensure completion and sending out Safety Data Sheets (SDS) and attending 3rd party audits.

This is an outstanding opportunity to join a leading Chemical Distributor who continues to have success across the UK and Europe. In return they offer an attractive salary and benefits package.

To be considered for this Regulatory Affairs Officer role, you will have a degree in Chemistry or a relevant discipline (or equivalent), demonstrated understanding & experience of working to chemical regulatory standards including ISO 9001, ISO 14001, OHSAS 18001 and REACH as well as knowledge of safety data sheets (SDS). Experience of auditing to ISO standards and/or within a supervisory or managerial function would be highly advantageous but it is not essential.

Apply Now

For more information, or to apply for this Regulatory Affairs Officer position, please contact Andrew Bolton at CK Science on 01438 870 013 or email abolton@ckscience.co.uk. Please quote reference ST20378 in all correspondence.

Alternatively, click here to apply for this Regulatory Affairs Officer position online now.


Meet Andrew – CK Science’s Specialist Chemical Industry Recruitment Consultant for the South, UK


Quality Assurance Officer (Chemical) – Hertfordshire, UK

Tuesday, June 22nd, 2010

A Quality Assurance Officer is required to join the Development and Manufacturing site of an innovative Polymer Chemical organisation based in Hertfordshire, UK.

Reporting directly to the General Manager, as Quality Assurance Officer, you will be responsible for the following:

  • Managing all quality systems and standards on site (ISO 9001, ISO 13485).
  • Ensuring environmental requirements (Health & Safety, COSHH).
  • Implementing internal audits as well as managing external auditors and ensuring the completion of all relevant quality documentation.

This is an excellent opportunity to work for an award winning Polymer Chemical organisation, who in return offers an attractive salary and benefits package.

To be considered for this Quality Assurance Officer role, you will have a degree in a scientific subject (or equivalent) and proven practical experience within a quality assurance (QA) function gained in the Chemical or a related industry including knowledge of ISO 9001 and ISO 13485.

 

 Apply now

For more information, or to apply for this Quality Assurance Officer job, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk.Please quote reference ST19959 in all correspondence.

Alternatively, click here apply for this Quality Assurance Officer job online now.

Medical Device Auditor – Hampshire, UK

Thursday, April 15th, 2010

Medical Device Auditor required for a world leading Medical Device Auditing Consultancy based in Hampshire, UK.

Our client, a world leading Medical Device Auditing Consultancy, are currently looking for an Auditor to join their busy and growing Auditing Team, based from their state-of-the-art facilities in Hampshire, UK.

Working as part of a multi-disciplinary team, as Medical Device Auditor, you will be involved in auditing medical device manufacturers and certifying their products against European standards (ISO 13485, MDD), as well as preparing and managing all relevant auditing documentation. As well as auditing and certification, you will also ensure that clients maximise the value and effectiveness of their quality systems. Due to the nature of this role some UK & Overseas travel is required.

This is an exciting opportunity to join a world leading Medical Device Auditing Consultancy, which in return offers an attractive salary and benefits package as well as a structured training program to develop the successful candidate in to a Lead Auditor.

The ideal candidate for this Medical Device Auditor job will have a degree in a relevant Scientific or Engineering discipline (or equivalent) and proven practical experience performing a Quality or Regulatory function within the Medical Device industry including demonstrated knowledge of the Medical Device Directives (MDD) and ISO 13485. Knowledge of a second European Language would be advantageous, but it is not essential.

How to Apply:

For more information, or to apply for this Medical Device Auditor job, please contact Andrew Bolton 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST19606 in all correspondence.

Alternatively, click here to apply for this Medical Device Auditor job now.

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CK Science - Science Jobs, Scientific Recruitment, UK

Quality Engineer based in Suffolk, UK

Wednesday, March 10th, 2010

Our client, a global industry leader in Consumer & Medical Device Technology, are currently looking for a Quality Engineer to work from their state-of-the-art Manufacturing facilities based in Suffolk.

Joining their Quality Engineering Team, you will be responsible for developing and implementing key manufacturing improvements in line with continual improvement activities such as 5S, Kaizen & Lean Manufacturing.

As a Quality Engineer, you will also be involved in conducting audits utilising a range of quality tools (FMEA, Control Plan, 8D, Lean) in line with relevant quality standards (ISO 13485, 19001) as well as implementing non conformance reports and root cause analysis in order to ensure corrective and preventative actions (CAPA) are taken.

This is an exciting opportunity to join a world leader in Technology Development & Manufacturing, which in return offers an attractive salary and benefits package as well as strong career progression.

To be considered for this Quality Engineer role, you will have a degree or equivalent in an Engineering or Scientific Discipline and proven practical experience within a Manufacturing and/or Medical Device Environment including Black Belt or the potential to achieve. Demonstrated experience of quality tools (FMEA, Control Plan, 8D, PPAP, DFSS, Lean Manufacturing) and knowledge of quality standards (ISO 13485, 19001) are essential for this role.

 

How to Apply

If you would like to hear more about this role, please contact Andrew Bolton on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST19410 in all correspondence.

Alternatively, you can click here to apply for this Quality Engineer job now.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.

 

About CK Science

CK Science is the largest independent scientific recruitment company in the UK. Our team of specialist recruiters are here to help you achieve your career ambitions within the scientific industry. We actively offer you careers advice, help with writing your CV, assistance with interview preparation and up-to-date information about the industry. We pride ourselves on providing an honest, straight-forward and trustworthy service to both our clients and candidates.

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