Posts Tagged ‘suffolk’

Associate Director Job (Pharmaceuticals, Quality Auditing) – Suffolk, UK

Tuesday, June 28th, 2011

We are currently looking for an Associate Director to join a global pharmaceutical company in the Suffolk region.

As Associate Director, you will be responsible for developing and managing audit programs for healthcare compliance and privacy at the company’s facilities to ensure they are meeting the relevant company and regulatory standards.

 

As Associate Director, you will also:

  • Develop and introduce a process for carrying out healthcare compliance audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management. 
  • Train company auditors in healthcare compliance auditing.
  • Auditing company facilities including country offices and relevant business units for healthcare compliance.
  • Develop and introduce a process for carrying out privacy audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management.  The audits will check that the organization can both meet the requirements of the company and the relevant regulatory requirements.
  • Train auditors in privacy auditing.
  • Auditing facilities for privacy.

 

Person specification:

The ideal candidate for this Associate Director position will have the following qualifications, skills and experience:

  • Possess a Bachelors degree (or equivalent) with related industry experience.
  • Extensive experience in auditing
  • Expert knowledge of healthcare compliance and/or privacy requirements for the pharmaceutical and/or medical device industries
  • Strong written and oral communication skills.

 

How to apply

For more information or to apply for this Associate Director position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST22200 in all correspondence.

 

Click here to apply online!

Not quite what you’re looking for? Search our current pharmaceutical jobs online now.

Senior QA Officer Job – Suffolk, UK

Tuesday, October 12th, 2010

Working within this busy Quality Assurance department based in Suffolk, as Senior QA Officer, you will be responsible for reviewing documentation in accordance with in-house specifications and cGMP.

Responsibilities:

As a Senior QA Officer, you will work to maintain and manage quality systems regarding cGMP for the site and support or perform audits and inspections to assure compliance with regulations. You will provide QA advice for deviation investigation and root causing, provide QA advice for change management and facilitate internal audits and inspections under direction and produces reports and action plans.

Qualifications and Experience:

The ideal candidate for this Senior QA Officer position will have demonstrated knowledge of working within a quality management system and cGMP and demonstrate the ability to successfully facilitate quality project work or audits.

This is a great opportunity to join a growing pharma company in the Suffolk region with excellent commuting links to Cambridge and the North.

Apply Now:

For more information, or to apply for this Senior QA Officer position, please contact Julie Marshall at CK Science on 01438 723 500 or email jmarshall@ckscience.co.uk. Please quote reference ST20551 in all correspondence.

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


Not quite what you’re looking for? Click here to search our current science jobs online now.

.

Senior QA Officer Job – Cambridgeshire, UK

Tuesday, August 31st, 2010

Our client, is a leading global biotechnology company based in the Cambridgeshire/Suffolk area, looking for a Senior Quality Assurance Officer to join their QA team.

As Senior QA Officer, you will be responsible for reviewing documentation in accordance to in-house specifications as well as cGMP. You will also provide QA advice for deviation investigation, root causing and change management. Part of the role will include internal auditing and supervision of less experienced staff.

To be successful for this Senior QA Officer role you will have a BSc in a scientific discipline (or equivalent). Previous experience with deviation investigation, batch release of API and dealing with customer complaints is essential. Experience in auditing or documentation review within a Quality Management System is also essential.

This is a fantastic opportunity to join a biopharmaceutical company within an easy commuting distance from Cambridge.

Apply Now

For more information, or to apply for this Senior QA Officer position, please contact Reena at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST20411 in all correspondence.

Meet Reena – Our Specialist Environmental and Food Recruitment Consultant (South, UK)


Senior Packaging Engineer – Suffolk, East Anglia, UK

Tuesday, April 27th, 2010

Senior Packaging Engineer required for blue chip global FMCG organisation based in Suffolk, East Anglia, UK.

As Senior Packaging Engineer, you will be responsible for the development of complete packaging concepts and specifications as well as project management of material testing and validation projects. Working with the process team, in this Senior Packaging Engineer, you will also be involved in the optimisation of process systems on site including the introduction of new technology for packaging application in line with GMP and ISO standards.

This is an amazing opportunity to join the FMCG division of a world leader operating in multiple markets. In return they offer an attractive salary and benefits package as well as structured career progression.

To be considered for this Senior Packaging Engineer role, you will have a BEng in Packaging Engineering, Mechanical Engineering, Manufacturing Engineering or a related subject (or equivalent experience) and demonstrated knowledge of packaging within the FMCG industry. This Senior Packaging Engineer job also demands a candidate with proven practical experience within a process engineering environment including implementing packaging projects. Entitlement to work in the EEA is essential.

How to Apply

For more information, or to apply for this Senior Packaging Engineer job, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST19576 in all correspondence.

Alternatively, click here to apply for this Senior Packaging 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.

Not quite what you’re looking for? Click here to search our current science job vacancies now.

CK Science - Science Jobs, Scientific Recruitment, UKTwitter - CK Science, Scientific Recruitment, Scientific Jobs, UKLinkedin - CK Science, Science Jobs, Scientific Recruitment, UKFacebook - CK Science, Science Jobs, Scientific Recruitment, UKYoutube - CK Science, Scientific 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.

CKS01twittercksciencelinkedinfacebook youtubeckclinical

Immunoassay Development Scientist based in South East, UK

Tuesday, February 2nd, 2010

Immunoassay Development Scientist based in South East, UK

Our client is involved in supporting healthcare providers and the pharmaceutical and biotechnology industries with technically advanced testing services. This innovative and dynamic company are currently looking for a “hands on” Immunoassay Development Scientist to join their team based in Suffolk, who is capable of developing new assays from concept through to validation and transfer to manufacturing. Reporting to the Head of Immunodiagnostics Development, you will be involved in the design and development of In-vitrodiagnostic devises using immunodiagnostic procedures.

Working as an Immunoassay Development Scientist, you will oversee the maintenance and growth of hybridomas for monoclonal antibody production and the purification of component materials from sources such as recombinant organisms, hybrodomas or other biological systems. You will also assist in the design, development and troubleshooting of all immunoassay development projects to verify and validate the product.

The successful candidate for this Immunoassay Development Scientist job will be educated to degree level or equivalent in a science related subject and that you have knowledge of working to GLP. Experience of analytical techniques such as ELISA, 2D electrophoresis, protein purification and cell culture is also essential.

If you would like to hear more about this Scientist job, please contact Lucy Campbell on 01438 723 500 or email lcampbell@ckscience.co.uk.  Please quote reference ST19177 in all correspondence.

Apply for this Immunoassay Development Scientist job now.

If you are successful after the first round of screening we will contact you within 5 working days. 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 ofspecialist 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.

CKS01linkedintwittercksciencefacebookckclinical youtube

Search for a job

Advanced search

20 years Download the CK Science iPhone App

Subscribe to our newsletter

Preview
Powered by FeedBlitz