Packaging Support Analyst – North East England

Our client, a blue-chip pharmaceutical company located in North East England, seeks an enthusiastic Packaging Support Analyst.

Responsibilities:

The successful candidate will be accountable for customer relationships and workload management for the launch of new packaging designs. The role also includes:

  • Working towards demanding deadlines you will coordinate the processing of new pack creations to meet customer requirements.
  • Keeping your clients informed of pack design progress.

Qualifications and Experience:

Ideally, the successful candidate will have experience gained in a packaging or relationship management environment and be of graduate calibre. A major part of the role will be liaising with colleagues and clients so excellent communication skills are essential as well as good time management.

Apply Now:

For more information or to apply for this Packaging Support Analyst position, please contact Heather Deagle on 0191 384 8905 or hdeagle@ckscience.co.uk. Please quote reference DH 22059 in all correspondence.

Click here to apply online!

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Regulatory Affairs Manager Job – North Scotland

Our client, a Scottish diagnostics company require a Regulatory Affairs Manager on a temporary basis to cover maternity leave.

Reporting to the Quality Assurance/Regulatory Affairs Director you will be responsible for a small team ensuring company activities are in compliance with regulations applicable to the diagnostics industry.

To be considered for this Regulatory Affairs Manager position, you must have the following skills and experience:

  • Have experience of working within or in close interaction with the RA team in relation to regulatory submissions or verification activities.
  • Be knowledgeable about the requirements of at least one of the following areas, IVD Directive, FDA 510k submissions, cGMP requirements as they impact on RA.
  • Have experience in interacting with external partners and regulatory agencies including the FDA.
  • Have the ability to build key relationships within the senior management team to promote and direct RA within the organisation.
  • Have supervisory experience.
  • Educated to degree level in a life science subject or have demonstrable experience in a regulatory affairs position.

 

How to apply

For more information or to apply for this Regulatory Affairs Manager position, please contact Graeme Pallas on 0191 384 8905 or email gpallas@ckscience.co.uk.

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Technologist Job – Oxfordshire, UK

CK Science is looking for a Technologist to join a world leading Medical Device organisation based in Oxfordshire.

As Technologist you will join the company’s Quality and Regulatory team and will be involved in the development of various medical devices and diagnostics products.

This is an excellent opportunity to work for a leading name in Medical Device development and manufacturing. In return, they offer a competitive package combined with strong career prospects.

Responsibilities:

Working as a Technologist, you will be responsible for carrying out complete device and component testing on a wide range of medical devices & diagnostic equipment using techniques such as AQLs, Force Tests, Wet Tests and Spring Testing. As part of the quality team, you will also be required to complete relevant quality documentation (ISO 13485, GMP) following testing and support internal and customer audits when required. 

Requirements:

To be considered for this role, you will have a qualification in a Scientific or Engineering discipline (or equivalent) and demonstrated experience in a device / component Testing or Quality role gained within the Medical Device, Diagnostic or a related technology industry.

How to apply

For more information or to apply for this Technologist position, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk. . Please quote reference ST22054 in all correspondence.

Click here to apply online!

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QA Officer – (Medical Device) Oxfordshire

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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UK and US collaboration could strengthen our science industries

As reported by The Manufacturer, Prime Minister David Cameron and President Barack Obama plan to bolster collaboration in science between the UK and US.

The partnership will involve the UK and US joining forces on a number of science research projects and will also work together to create the world’s first combined first space weather model. The agreement also sees the US company Johnson & Johnson investing £5 million into a partnership with six leading British universities in order to help them undertake cutting edge neuroscience research.

Speaking of the collaboration, David Willetts, Universities and Science Minister stated,  “Our most productive science and higher education relationship is with the US and we are determined to strengthen it further. As globalisation gathers pace international cooperation in these areas has become even more important to boost Britain’s economic growth, and they are a key part of our overall relationship with the United States.”

Are you looking for a new position in science? Click here to search our current science jobs online now.

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QA Specialist Job – Scotland

Our client is a pharmaceutical company based in North Scotland and are looking for a Quality Assurance Specialist to join their team.

Job purpose

Your role will involve driving a quality culture throughout the site ensuring products and services meet the necessary expectations and regulatory requirements. To ensure the quality of materials, suppliers, products and components (primary and secondary); services related to productions; production and inspection processes meet the expected regulations.

Responsibilities

You will be responsible for providing assurance that all operations, processes and procedures are performed in compliance with applicable regulations, including approved SOPs (and GOPs) and GMP documentation. Creating, monitoring and maintaining quality standards for the site.

Other duties include:

  • Provide support and oversee the maintenance and operations of the quality systems such as TrackWise Change Control, Deviation and CAPA .
  • Provide support and oversee theExternal and Internal Complaints systems.
  • Provide support and manage the site’s SOP Scout system.
  • Review data and produce review documents, such as Product Quality Reviews/Annual Quality Reviews, Customer Complaint Reviews, Deviation Reviews.
  • Support Validation Activities.
  • Report workload and keep the Quality Management Team informed.
  • Deputise for Quality Team Leader.

 

Apply now

If you do not hear back from us within 5 working days of your application for this role, it means that onthis occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference DH21508 in all correspondence.

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Quality Engineer Job – (Medical Device) Hampshire

Our client is a world renowned Medical Device organisation who develop innovative & industry leading devices. They are currently looking for a Quality Engineer to join their QA & RA Division based from their site in Hampshire.

Responsibilities:

Working as a Quality Engineer, you will be responsible for working across the Production, Development & Quality internal teams as well   as external suppliers.

Your duties will include:

  • Developing, creating and maintaining regulatory & quality system (ISO 13485, ISO 9001, Medical Device Directives) documentation
  • Developing & carrying out equipment & process validation
  • Aiding with transfer of new products to manufacturing
  • Carrying out non-conformance & root cause analysis and implementing corrective actions as well as assisting with internal & external (customer & supplier) audits
  • In addition to your duties in the Medical Device side, you will also be involved in supporting a small pharmaceutical division as and when required.

This is an outstanding opportunity to join a blue chip Medical Device organisation, which in return offers an attractive salary, an excellent bonus scheme and benefits package.

Qualification and Experience:

To be considered for this role, you will have a demonstrated background in a Quality Engineer or related Regulatory Engineering  function gained within the Medical Device, Pharmaceutical, Biotechnology or a relevant industry.

Apply now:

For more information or to apply for this Quality Engineer position, please contact Andrew Bolton on 01438 723 500 or abolton@ckscience.co.uk. Please quote reference ST21952 in all correspondence.

Click here to apply online

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CK are exclusively recruiting for ACAL Energy!

[youtube]http://www.youtube.com/watch?v=MFW7oh6sCR4[/youtube]

ACAL Energy Ltd is based in Runcorn, Cheshire, and is currently working on an exclusive basis with CK Science to recruit a variety of scientists and engineers outlined below. Please direct any queries to Vicki at vwalker@ckscience.co.uk or on 0114 283 9956, quoting the appropriate reference number for the vacancy you wish to enquire about.

ACAL Energy Job Vacancies:

Please find links to the currently available vacancies with ACAL Energy Ltd below:

 

 

About ACAL Energy

ACAL Energy Ltd is the world’s leading developer of low cost Proton Exchange Membrane (PEM) Fuel Cells systems, powered by ACAL Energy’s proprietary platinum free cathode technology (FlowCath®).

ACAL Energy Ltd is a developer of Fuel Cell systems, modules and consumable chemicals for a range of uses including stationary, residential and automotive applications. Its innovative designs will deliver substantial cost savings and performance improvements that will accelerate the adoption of PEM Fuel Cell technologies in key markets.

Fuel Cells are electrochemical systems that convert chemical energy to electrical power directly. They offer a clean and efficient technology for the generation of electricity and are poised to become the leading energy source of the 21st century in a range of applications.ACAL Energy has been announced as one of the winners of the Carbon Trust’s Polymer Fuel Cell Challenge competition, leading to a funded project intended to deliver the critical reduction in fuel cell system costs that must be achieved to make mass market deployment a reality.  The company employs leading scientists and engineers in the Fuel Cell arena and is now looking to expand the team to support this program of work.

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Senior Regulatory Affairs Officer Job – Scotland

Click here to apply online!

Our client, a world-leading manufacturer of diagnostic reagents are looking for a Senior Regulatory Affairs officer to join their team in Scotland.

 

Responsibilities:

As Senior Regulatory Affairs Officer, you will be responsible for managing, preparing and maintaining regulatory documentation to enable the company to comply with ISO9001 and ISO13485 standards and to ensure on-going regulatory compliance to GMP. You will also be responsible for gaining CE marking for new products in the EU, registration via competent authorities and FDA approval for products in the US, while maintaining existing licences and registrations.

Further responsibilities include:

  • Plan, co-ordinate, prepare and interpret relevant information necessary for product licence applications to ensure successful granting, maintenance and development of such licenses by Regulatory Authorities on a world wide basis.
  • Advise staff on data and information required for successful license applications and co-ordinate their efforts to ensure that their contributions to regulatory applications are produced to an appropriate standard for submission.
  • Compile product information for the preparation of technical files and regulatory dossiers to support product licence applications and product license maintenance for world wide Regulatory Authorities.
  • Ensure that changes are communicated as appropriate to the Regulatory Authorities
  • Liaise with regulatory agencies and external contract bodies and, in response to requests from these, to collate and interpret specialised information
  • Provide advice on the licensing options/regulatory requirements for the company, to facilitate process/product modifications
  • Contribute to the design and implementation of new systems and procedures and identify areas for potential improvement to ensure the concept of continuous quality improvement is realised
  • Participate as required in the selection and recruitment of new staff and participate in induction programmes for new starts in relation to Regulatory Affairs

 

Qualification and Experience:

The ideal candidate for this Senior Regulatory Affairs Officer position must hold a relevant degree or professional qualification and an appropriate level of experience in a Regulatory Affairs environment, significant specialist knowledge of Regulatory Affairs and an understanding of the operation of a medical device manufacturing establishment (ideally as applied to in vitro diagnostic medical devices).  As well as the ability to analyse information in a structured manner and to be able to prepare coherent regulatory reports and filings.

Apply now

For more information or to apply for this Senior Regulatory Affairs Officer position, please contact Carrie Ann on 0191 384 8905 or cbell@ckscience.co.uk. Please quote reference DH21857 in all correspondence.

Click here to apply online!

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CK Science are looking for a Trainee Recruitment Consultant to join their team!

Click here to apply online now!

CK Science is a leading independent scientific recruitment consultancy for science jobs.  Part of the CK Group, CK Science’s highly trained, specialist scientific recruitment consultants are here to help candidates and clients with their recruitment needs within the scientific, chemical, pharmaceutical, biotechnology, food, waste, environmental, and other related industries.

We currently have a vacancy within our Chesterfield office for a Trainee Scientific Recruitment Consultant. From the Chesterfield office we provide permanent and temporary recruitment solutions to companies employing scientists and engineers in the North of England, the Midlands, Wales and Ireland.

This is a sales orientated position with extensive people contact, both face to face and by telephone. We are looking for an outgoing individual with lots of personality who is hungry for success and will enjoy the satisfaction of providing a quality, professional service to both clients and candidates.  The role will focus on permanent recruitment services for the life sciences industry.

To be considered for this role you should have a degree in a scientific or technical discipline (or equivalent experience) as you will be liaising with scientists and engineers on a technical level. A background in sales or recruitment would be beneficial. In any case, you must have excellent communication skills combined with self-confidence and a professional approach.

Apply now

For more information or to apply for this Russell Oakley at CK Science on 0114 283 9956 or email roakley@ckscience.co.uk. Please quote reference SH21966 in all correspondence.

 

Click here to apply online now!

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Technical Manager Job – North East England

Click here to apply online now!

 

Our client is an innovative device manufacturer based in the North East of England. They require an experienced Technical Manager with experience of running multifaceted projects in X-ray instrumentation for medical imaging and airport security.

Responsibilities:

As Technical Manager, you will use your technical expertise to work closely with customers in delivering development projects on existing products and from scratch.  This will involve managing teams, co-ordinating departments and resources, costing raw materials and overall project delivery and technical support.

Candidate requirements:

You must be qualified to minimum BSc in physics or engineering or possess equivalent industrial experience. You must also possess a strong track record in managing projects within X ray or similar technology.

Apply now

For more information or to apply for this Technical Manager position, please contact Barney Smith at CK Science on 191 394 8905 or email bsmith@ckscience.co.uk. Please quote reference DH21947 in all correspondence.

Click here to apply online now!

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Product Engineer Job – North East of England

Click here to apply online now!

 

Our client is a market leader in x ray instrumentation. They require a Product Engineer to join their expanding team based in the North East of England.

Responsibilities:

As Product Engineer, you will be responsible for providing technical service and support to new and existing clients. This will involve providing support in installation, maintenance, troubleshooting and providing technical advice and expertise. You will work both on site and remotely responding to customer queries and complaints providing a full and comprehensive service.

Candidate requirements:

The ideal candidate for this Product Engineer role, must be qualified to minimum degree level in a relevant area of physics such as x ray or condensed matter or possess equivalent industrial experience. You must also possess excellent data analysis and programming skills, experience in handling commercial tenders and a proven track record in technical service and troubleshooting.

Apply now!

For more information or to apply for this Project Engineer job, please contact Barney Smith at CK Science 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH21951 in all correspondence.

Click here to apply online now!

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Material Test Technician Jobs

[youtube]http://www.youtube.com/watch?v=vp-CWE_Mceo[/youtube]

CK Science are currently working with a number of clients in the polymer industries who are looking for Material Test Technicians to join their workshops and material testing labs.

Within these Material Test Technician roles you will test a wide range of polymeric materials using physician, mechanical, climatic and chemical testing.

We are looking for candidates who have qualifications in Polymer Science, Technology or Chemistry and who have experience of working in a workshop or material test laboratory. If this sounds like you, please contact Andrew Bolton on 01438 723 500 or email abolton@ckscience.co.uk.

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Senior Medical Device Technologist Job

We are currently searching for a Senior Medical Device Technologist to join a global Medical Device company based in Oxfordshire, UK.

Responsibilities:

As Senior Medical Device Technologist your key responsibilities will include:

  • Providing technical support to the NPI (New Product Introduction) for the diabetes strip-manufacturing unit and supporting the unit to maintain production output and yields.
  • Ensuring the analysis and interpretation of measurements in process and release test data, identify potential areas of inefficiency to drive continuous process, product, cost and quality improvements in the manufacturing unit.
  • You will also ensure all work carried out in compliance with the correct processes and procedures and take ownership ofassigned ER’s CAPA’s and VMP activities.

 

Requirements:

For this role you will be degree qualified in a scientific/engineering discipline (or equivalent) with previous experience in Validation.

Previous knowledge of relevant processes, test methods, analytical techniques, experimental design, data analysis and statistical process control would be advantageous. You will have a good understanding of cGMP in Design Control and Validation.

Understanding the principles behind Six Sigma and Continuous Improvement methodologies is essential and have excellent communication and IT skills. Previous experience in a highly regulated industry would be advantageous.

Apply now

For more information or to apply for this Senior Medical Device Technologist position, please contact Reena Dhana at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST21881 in all correspondence.

 

Click here to apply online!

 

Posted in Jobs

Medical Device Technologist Job – Oxfordshire, UK

CK Science are currently searching for a Medical Device Technologist to join a global Medical Device company based in Oxfordshire, UK.

 

Responsibilities:

As Medical Device Technologist, your key responsibilities will include:

  • Providing technical support to the NPI (New Product Introduction) for the diabetes strip-manufacturing unit and supporting the unit to maintain production output and yields.
  • Ensuring the analysis and interpretation of measurements in process and release test data, identify potential areas of inefficiency to drive continuous process, product, cost and quality improvements in the manufacturing unit.
  • You will also ensure all work carried out in compliance with the correct processes and procedures and take ownership of assigned ER’s CAPA’s and VMP activities.

 

Requirements:

The ideal candidate for this Medical Device Technologist role you will have a degree qualification in a scientific/engineering discipline (or equivalent). Previous knowledge of relevant processes, test methods, analytical techniques, experimental design, data analysis and statistical process control would be advantageous. You will have a good understanding of the concept and importance of GMP. Have excellent communication and IT skills.

Apply now

For more information or to apply for this Medical Device Technologist position, please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk.Please quote reference ST21882 in all correspondence.

Click here to apply online!

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Senior Quality Assurance Officer Job – Suffolk

A leading biotechnology company are currently looking for a Senior Quality Assurance Officer to join their team based in Suffolk.

As Senior Quality Assurance Officer you will act as a liaison between company plants and contractors bulk and components supplied by the plants to the contractors.

Responsibilities:

  • Modifying, auditing, and ensuring contractor quality standards and protocol for processing materials into partially finished or finished product.
  • Implementing methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
  • Responding to technical and quality issues and assists in resolving schedule conflicts.
  • Specifying inspection and testing mechanisms and equipment.
  • Conducting contractor quality assurance audits and performing statistical analysis; ensuring that the product is available to meet company needs.
  • Coordinating the development of documentation for contractor manual.
  • May assist in vendor selection and evaluation.

 

Requirements:

  • You will be required to work under very general supervision and follow established procedures.
  • You will interact with Operation, project teams and research groups as they impact the quality operation.
  • You will have a broad knowledge of EU/UScGMP’s for the biotech/ pharmaceutical industry, with an understanding of worldwide regulatory affairs.
  • Experience in Quality Assurance with focus on product release, auditing and quality oversight of contractor manufacturers.
  • Additional knowledge of and background in Quality Control techniques and testing methodologies is beneficial.

 

Apply now

For more information or to apply for this Senior Quality Assurance Officer job, please contact Julie Marshall on 01438 723 500 or email jmarshall@ckscience.co.uk. Please quote reference ST21895 in all correspondence.

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Quality Manager Job – Scotland

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.

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

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Senior Regulatory Affairs Officer Job – Scotland, UK

Our client, a world-leading manufacturer of diagnostic reagents are looking for a Senior Regulatory Affairs Officer to join their team in Scotland. 

Responsibilities:

As a Senior Regulatory Affairs Officer, you will be responsible for managing, preparing and maintaining regulatory documentation to enable the company to comply with ISO9001 and ISO13485 standards and to ensure on-going regulatory compliance to GMP.

You will also be responsible for gaining CE marking for new products in the EU, registration via competent authorities and FDA approval for products in the US, while maintaining existing licences and registrations.

Your role will require you to:

  • Plan, co-ordinate, prepare and interpret relevant information necessary for product licence applications to ensure successful granting, maintenance and development of such licenses by Regulatory Authorities on a world wide basis.
  • Advise staff on data and information required for successful license applications and co-ordinate their efforts to ensure that their contributions to regulatory applications are produced to an appropriate standard for submission.
  • Compile product information for the preparation of technical files and regulatory dossiers to support product licence applications and product license maintenance for world wide Regulatory Authorities.
  • Ensure that changes are communicated as appropriate to the Regulatory Authorities
  • Liaise with regulatory agencies and external contract bodies and, in response to requests from these, to collate and interpret specialised information
  • Provide advice on the licensing options/regulatory requirements for the company, to facilitate process/product modifications
  • Contribute to the design and implementation of new systems and procedures and identify areas for potential improvement to ensure the concept of continuous quality improvement is realised
  • Participate as required in the selection and recruitment of new staff and participate in induction programmes for new starts in relation to Regulatory Affairs

 

Requirements:

The successful applicant for this Senior Regulatory Affairs Officer position will hold a relevant degree professional qualification.

You will also have an  appropriate level of experience in a Regulatory Affairs environment, significant specialist knowledge of Regulatory Affairs and an understanding of the operation of a medical device manufacturing establishment (ideally as applied to in vitro diagnostic medical devices). 

In addition, you will have the ability to analyse information in a structured manner and to be able to prepare coherent regulatory reports and filings.

Apply now

For more information or to apply for this Senior Regulatory Affairs Officer position, please contact Carrie-Ann Bell on 0191 384 8905 or email cbell@ckscience.co.uk. Please quote reference DH21857 in all correspondence.

Posted in Jobs

Senior Assay Development Scientist Job – London

Our client is an innovative Diagnostic Technology organisation who specialises in applications including in-vitro diagnostics, biodefence and environmental testing. They are currently looking for a Senior Assay Development Scientist to head up their Assay Development Team based from their site in London.

This is an outstanding opportunity to join an innovative Diagnostic Technology organisation, which is at the forefront of biosensor diagnostics. In return they offer a negotiable salary depending on experience and excellent benefits.

Responsibilities:

As the Senior Assay Development Scientist, you will be responsible for management of a team involved in the design and development of immunoassays; integration of immunoassay reagents with optical detection systems based on fluorescent, phosphorescent and absorbance measurement and with microfluidic analysis platforms; immobilisation of antibodies onto a variety of solid substrates as well as liaising with other internal divisions throughout the projects.

Requirements:

To be considered for this Senior Assay Development Scientist role, you will have a degree / PhD in Chemistry, Biochemistry or a relevant biomedical science (or equivalent) and thorough knowledge of immunoassay design & development and demonstrated people management experience. Experience of biosensor technology and microfluidics is desirable but it is not essential.

Apply now

For more information or to apply for this Senior Assay Development Scientist job, please contact Andrew Bolton at CK Science 0on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST21902 in all correspondence.

Apply online!

Click here to apply online now.

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Asbestos Surveyor and Analyst Jobs

Our client is a large organisation with offices all over the UK.  They require Asbestos Surveyors and Analysts to join their teams due to an increase in workload.

Currently there are immediate requirements for P401, P403 and P404 level Analysts in the midlands and P402 level Surveyors in the central belt of Scotland.  If you are qualified to Pcert standards and looking for surveying or analytical opportunities then please get in touch.  Entitlement to work in the UK is essential.

Apply now

For more information or to apply for these Asbestos Surveyor and Analyst positions, please contact Barney Smith at CK Science on 0191 384 8905 or email bsmith@ckscience.co.uk.

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