 |
| Job Title |
|
Regulatory Affairs Assistant - Medical Device |
| Location |
|
Oxfordshire |
| Job Number |
|
120262130 |
| Posted |
|
25/05/2012 (17:22) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
Description
|
|
Reena Dhana at CK Science is currently recruiting for a Regulatory Affairs Assistant, Medical Device to join a Pharmaceutical Organisation at their site in Oxfordshire on a full time, 6 month contact.
As a Regulatory Affairs Assistant the main purpose of your role will be:
- Supporting the RA team and International Commercial team to organise, prepare and assist with submitting documentation for international product registrations in a timely manner.
- Supporting the Regulatory team in assigned Regulatory projects.
- Assist the RA team in the coordination and preparation of documentation with the Corporate Legal team.
As a Regulatory Affairs Assistant you will have the following qualifications, skills and experience:
- Previous experience in a Quality or Regulatory role within the Medical Device industry is essential.
- Working knowledge of regulations such as ISO13485, MDD Medical Device Directives is also essential.
As a Regulatory Affairs Assistant, you will be joining a Global Pharmaceutical Organisation who in return are offering a competitive salary.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24391 in all correspondence.
Keywords: Pharmaceutical Jobs, Medical Device, Oxfordshire, Regulatory Affairs, ISO 13485, Reena Dhana
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| Job Type |
|
Contract |
| Contract Length |
|
0 - 6 months |
| Start Date |
|
ASAP |
| Contact Details |
|
 |
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| Job Title |
|
Laboratory Manager - Blood, Diagnostics |
| Location |
|
Cambridge, Cambridgeshire |
| Job Number |
|
120262125 |
| Posted |
|
25/05/2012 (17:11) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Reena Dhana at CK Science is currently recruiting for a Laboratory Manager to join a global Medical Device organisation based in Cambridgeshire on a full time, rolling contract opportunity.
As a Laboratory Manager, you will be responsible for designing and setting up a laboratory for the testing of blood based samples to support their R&D projects on site. Your duties will include:
- Carrying out initial evaluation of requirements for the potential laboratory including equipment, facilities, staff, budget, quality standards and other related aspects.
- Putting together technical proposals & reports for the laboratory.
- Once requirements are established, working closely with multi-disciplinary teams during the implementation & integration of the laboratory on site.
As a Laboratory Manager, you will have the following skills & experience:
- Demonstrated experience in a Laboratory Management / Technical Management function gained within a blood or related bio-sample testing environment.
- Previous experience in designing and/or implementing in part or full new laboratory facilities would be advantageous but it is not essential.
As a Laboratory Manager, you will be joining a leading name in the field of Medical Devices which in return offers an attractive salary / contract rate and with long term prospects of a permanent opportunity running the laboratory if established.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from uswithin 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. Please quote reference ST24412 in all correspondence.
Keywords: science jobs, laboratory manager, blood, diagnostics, medical device, Cambridgeshire, Reena Dhana
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| Job Type |
|
Contract |
| Contract Length |
|
0 - 6 months |
| Start Date |
|
ASAP |
| Contact Details |
|
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| Job Title |
|
Clinical Development Scientist |
| Location |
|
West London, London |
| Job Number |
|
120262124 |
| Posted |
|
25/05/2012 (17:06) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Our client is a global pharmaceutical manufacturer based in the UK. The company are currently looking to recruit a Clinical Development Scientist to work in the Metabolic Pathways and CardioVascular team. The company's Phase 2-4 project teams focus on the development of MPC medicines post Proof of Concept through to drug submission, with some post marketing support. We are looking for an experienced and innovative Clinical Development Scientist to join an established team to start as soon as possible.
This is a study management role within a large cardiovascular outcomes trial. The successful candidate will be required to work as part of a large global multi-functional team in collaboration with a CRO and Academic Research Organisation (ARO).
We would welcome applications from candidates with a minimum of 2 years regional / global study management plus 2 years CRA experience. A proven track record and ability to work in the following areas is desirable:
Experience of large outcomes studies
Serve as single point of contact for country/site questions relating to study operational issues; liaise with appropriate study team members as needed.
Management and oversight of CROs and other outsourcing partners
Maintain relationships and monitor the quality and performance of CROs & other vendors.
Ability to identify site quality issues, escalate as appropriate and help create solutions.
Experience of data delivery for interim analyses and /or delivery of database freeze
Experience of subject retention activities
Additional skill requirements:
- Solid understanding of R&D and drug development process and ICH GCP
- a proven track record of study management of complex projects including effective planning, negotiation and liaison with external vendors and internal clients
- the ability to take a holistic view of a project whilst using study management expertise to identify and solve problems
- effective communication with colleagues at all levels within a matrix team
- an ability to establish a rapport / build relationships with customers and partners (including monitoring staff) to influence relationships and implement change
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference CL24411 in all correspondence.
Keywords: Clinical, Recruitment, CV, Cardiovascular, Metabolic, Project Management.
|
| Job Type |
|
Contract |
| Contract Length |
|
6 months + |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
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| Job Title |
|
Customer Communications Coordinator |
| Salary/rate |
|
£30000 - £35000/annum |
| Location |
|
East Midlands |
| Job Number |
|
120262118 |
| Posted |
|
25/05/2012 (17:01) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
My client is looking to recruit a Customer Communications Communicator to work at their site in East Midlands on a permanent basis.
Specifically, this role will cover the Medical Device area and you will be handling all communication activities globally. You will be expected to work both independently and within a multifunctional team, and will be coordinating and supporting marketing and communication activities and branding. You will also be responsible for campaign execution and content supply in terms of copy and market research, and for being proactive in suggesting new communications ideas and activities.
Qualifications
- The successful candidate will have a degree in life science or equivalent.
- Team player with good communication and scientific/creative writing skills.
- Good practical knowledge of Medical Devices is essential.
- Experience in marketing communications activities and execution (both online and offline campaigns) would be beneficial.
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. Please quote reference SH24403 in all correspondence.
Keywords: science jobs, Medical Device, life science, marketing, communication
|
| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
ASAP |
| Contact Details |
|
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| Job Title |
|
Development Chemist - Colour, Cambs |
| Salary/rate |
|
£20000 - £30000/annum |
| Location |
|
Cambridgeshire |
| Job Number |
|
120262113 |
| Posted |
|
25/05/2012 (16:55) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Reena Dhana at CK Science is currently recruiting for a Development Chemist - Colour to join a Materials Manufacturing Organisation at their site in Cambridgeshire on a full time, weekly rolling contract.
As a Development Chemist - Colour the main purpose of your role will be:
- Carrying out routine testing of coating formulations and colour matching.
As a Development Chemist - Colour you will have the following qualifications, skills and experience:
- BSc in Chemistry or related subject (or equivalent)
- Previous experience of coating formulations and colour matching is essential.
As a Development Chemist - Colour, you will be joining a Global Pharmaceutical Organisation who in return are offering a competitive salary.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24405 in all correspondence.
Key words: Colour, Colour Matching, Colour Chemist, Formulation Coatings, Chemical, Chemistry jobs, Reena Dhana, Cambridgeshire
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| Job Type |
|
Contract |
| Contract Length |
|
0 - 6 months |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
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|
|
| Job Title |
|
Laboratory Analyst - Waste & Environmenal, Yorks |
| Salary/rate |
|
£17000 - £20000/annum |
| Location |
|
South Yorkshire |
| Job Number |
|
120262092 |
| Posted |
|
25/05/2012 (16:11) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Laboratory Analyst - Waste & Environmenal, Yorks. Our client, a hazardous waste and environmental management company based in the Yorkshire region, is currently looking to employ a laboratory analyst on a permanent basis.
The main roles and responsibilities of this Laboratory Analyst position will be to cover all the analytical requirements of the business and in conjunction with the site operations, ensure the efficient flow of waste through the site.
The role will cover:
-Analysis of waste received into Waste Management Centre for compliance, pre-acceptance, processing and monitoring.
-Laboratory instrument calibration.
-Closer interaction with operational team.
-Report analysis results using site procedures and methods.
-Ensuring safe and compliant operation in accordance with company policies and regulatory requirements.
-Deputising for Site Chemist as and when required.
In order to be considered for this Laboratory Analyst role, you will be educated to a minimum of HNC or equivalent in Chemistry, preferably with a degree or equivalent in chemistry. Previous experience of laboratory work and/ or waste management experience is advantageous. The ability to work as a committed, flexible and pragmatic team player with a professional approach is essential.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference SH24408 in all correspondence.
Keywords: lab chemist, site chemist, lab analyst, laboratory analyst, waste chemist, environmental, science recruitment, scientific recruitment
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| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
|
| Contact Details |
|
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| Job Title |
|
Sales Manager - Chemical, Electronics, UK, Ireland |
| Salary/rate |
|
£40000 - £45000/annum |
| Location |
|
United Kingdom, UK |
| Job Number |
|
120262067 |
| Posted |
|
25/05/2012 (13:55) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
CK Science are currently recruiting for a Sales Manager to join a world leading Chemical Manufacturer on a full time, permanent basis. This role is field based, with flexibility to be based anywhere within the UK & Ireland.
As a Sales Manager, you will be responsible for driving forward sales for the organisation's range of chemical products including adhesives, sealants & coatings to customers within the Automotive, Aerospace, Electronic, Medical Technology and related industries.
Your duties will include:
- Development of sales strategies to drive growth within the sales territory.
- Technical sales for the full range of chemical products, including dealing with customer contacts from shop floor to executive level.
- Key account management of an established customer base.
- Attending visits to customers sites.
- Working closely with internal technical teams including visits to sites within the UK & Europe.
As a Sales Manager, you will have the following qualifications, skills & experience:
- A qualification in a Scientific, Engineering or related Technical discipline (or equivalent).
- Demonstrated experience in a technical (scientific or engineering) environment / function within a Chemicals or Electronics sector.
- Experience in a sales / commercial function would be advantageous, but it is not essential.
As a Sales Manager you will be joining a global Chemical Manufacturer, which in return offers a salary of between £40,000 - £45,000, coupled with strong OTEs / bonus scheme and excellent benefits including company car, laptop, phone, pension and private medical care.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24407 in all correspondence.
Keywords: Science Jobs, Sales Manager, Chemical, Electronics, UK, Ireland, Field Based
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| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
|
| Contact Details |
|
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| Job Title |
|
Modelling & Simulation Group Manager |
| Salary/rate |
|
£40000 - £50000/annum |
| Location |
|
South East |
| Job Number |
|
113605556 |
| Posted |
|
25/05/2012 (13:52) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Modelling & Simulation Group Manager
South East
Permanent
£40,000-£50,000
Modelling & Simulation Group Manager require to grow and develop a small team of engineers for a leading Research and Consultancy company.
The successful Modelling & Simulation Group Manager will either be an experienced Manager or Senior Consultant Engineer educated to MSc or PhD level with strong background and interest in modelling and simulation related to fluids engineering.
Requirements:
Technical use of modelling and simulation
CFD, FEA, Flowmaster and other mathematical and simulations tools experience
Leadership abilities and technical direction to a team of engineers
Modelling & Simulation Group Manager Key Requirements:
Extensive experience in the application of modelling and simulation technology
Strong design and performance improvements experience related to chemical, mechanical or environmental ‘fluids’ engineering.
Industry insights and established contacts within either Aerospace and Defence, speciality chemicals and pharmaceuticals, nuclear and fossil power, water, wastewater and desalination, food, beverage and personal care, renewable energy, oil and gas.
MSc or PhD in Engineering, or other numerical field with solid knowledge of fluid dynamics.
Proven experience in using commercial software ANSYS Fluent, Open Foam, Flowmaster
Business and Commercial experience of planning and acquiring new business accounts
Rewards:
In return this opportunity offers the successful Modelling & Simulation Group Manager a competitive salary and the chance to build and lead the growth of this newly formed Modelling and Simulation Group in a senior management role.
CK IT is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference IT24406 in all correspondence.
|
| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
|
| Contact Details |
|
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| Job Title |
|
Process Technologist - Metallurgist, North West |
| Location |
|
North West |
| Job Number |
|
120262066 |
| Posted |
|
25/05/2012 (13:50) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Process Technologist - Metallurgist, North West. Our client, a manufacturer of specialist metals and materials based in the North West, is currently looking for a Process Technologist/ Metallurgist to join their team.
The main roles and responsibilities of this Process Technologist/ Metallurgist position will be to provide technical support to the manufacturing process on site. With the aim of becoming the company's technical specialist in the metallurgy, manufacturing and application of tungsten alloys, you will conduct process improvement trials to establish the best parameters for reliably manufacturing to specification. Responsible for analysing manufacturing data and ascertaining process performance & best practice, you will undertake raw material investigations and will develop the QC system. You will take responsibility for the metallurgy laboratory and will test samples of alloys and analyse the results. As well as specifying alterations to the manufacturing process and assisting with the commissioning of any new equipment, you will also troubleshoot process issues and will provide materials science support to manufacturing and applications departments.
In order to be considered for this Process Technologist/ Metallurgist role you will be educated to degree level or equivalent in Metallurgy or Material Science with additional experience gained within industry in a manufacturing environment. HNC/ HND or equivalent in Metallurgy or Materials Science may be considered if accompanied by considerable industrial experience gained within a manufacturing environment. Ideally you will be a member of a relevant professional body and will have experience of production trials or working on process improvement projects and alloy testing. Candidate should be confident in working with spreadsheets and be used to handling and manipulating data, as well as giving presentations. You should be able to explain technical issues to non-technical staff. This role may have the requirement to travel abroad for short-duration visits.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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 UK is essential. Please quote reference SH24396 in all correspondence.
Keywords: metals analysis, science recruitment, chemistry jobs, metallurgist, metallurgy, metallurgical, process technologist, material science
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| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
ASAP |
| Contact Details |
|
|
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|
|
| Job Title |
|
Laboratory Technician - Environmental, Manchester |
| Salary/rate |
|
£12000 - £13000/annum |
| Location |
|
Manchester, Greater Manchester |
| Job Number |
|
120262065 |
| Posted |
|
25/05/2012 (13:46) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Laboratory Technician - Environmental, Manchester. Our client, a contract testing facility based in Manchester, is currently looking to recruit a Laboratory Technician to join their environmental testing department. The company anticipates that this Laboratory Technician will progress to Senior Technician level within 3-6 months, eventually leading a team of 2 other technicians.
The main responsibilities of this Laboratory Technician role will be to perform all laboratory tasks and be answerable to the current Senior Technician and Senior Analyst. You will be responsible for sample preparation, solvent extractions using various matrices, stock control, chemical reagent preparation, glassware cleaning and other general laboratory duties.
In order to be considered for this Laboratory Technician position, you will ideally be educated to degree level or equivalent in chemistry or a related discipline, however GCSEs in English, Mathematics and Science at grade C or above is the minimum requirement. No experience is necessary as full in-house training will be given, however laboratory awareness/ training would be a distinct advantage. This role is practical and hands-on role, with the vast majority of time spent in the lab. Excellent interpersonal skills are required in order to progress to Senior Technician lever and you must be able to work well both in a team and solo.
Please note the starting salary for this role is £12-13,000pa depending on expereince.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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 UK is essential. Please quote reference SH24398 in all correspondence.
Keywords: science recruitment, chemistry jobs, laboratory technician, junior technician, junior chemist, lab technician, senior technician, environmental testing
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| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
|
| Contact Details |
|
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|
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| Job Title |
|
SAP Co-ordinator |
| Salary/rate |
|
£500 - £600/day |
| Location |
|
Suffolk |
| Job Number |
|
113605554 |
| Posted |
|
25/05/2012 (13:40) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
SAP FICO co-ordinator
Home Counties
9 months
£500-£600
Immediate start
SAP FICO co-ordinator required to join a global pharmaceutical company for a 9 month contract role based at the companies home counties site.
The successful SAP FICO co-ordinator will have an in depth knowledge and appreciation of SAP FI/CO and have a background in Finance with ideally some pharmaceutical/manufacturing knowledge.
SAP FICO co-ordinators responsibilities will include:
Working and coordinating with the companies internal SAP support team
Coordinating a smooth transition of the companies current processes across to their SAP standard platform:
Some of theses financial processess will include:
Financial master data
Suppliers and Customers repository Invoices control, Accounts payable, accounts receivable
Accounting
Assets management
Actual costs allocations
Closing processes
In addition to the above this SAP FICO role will involve:
Gap analysis MFG Pro vs SAP
Co-ordination of SAP FICO Change Management ( processes)
Lead the UAT
Training and supporting of the Key-users in all supported Sites
Key skills:
The successful SAP FICO co-ordinator will possess the following
Extensive practical working experience with SAP FI/CO modules
Experience with Finance/Accounting and understanding of the business processes within a Pharmaceutical/Manufacturing environment
Good Project Management skills
Knowledge of MFG Pro is an asset
CK IT is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference IT24380 in all correspondence.
|
| Job Type |
|
Contract |
| Contract Length |
|
6 months + |
| Start Date |
|
ASAP |
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
QC Laboratory Assistant, Chemical - London |
| Location |
|
London |
| Job Number |
|
120262048 |
| Posted |
|
25/05/2012 (11:30) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Reena Dhana at CK Science is currently recruiting for a QC Laboratory Technician to join a Chemical Organisation in Paints and Coatings at their site in London on a full time, weekly rolling contract.
As a QC Laboratory Technician the main purpose of your role will be:
- Carrying out routine testing on mastics, pastes, compounds and liquid coatings.
As a QC Laboratory Technician, you will have the following qualifications, skills and experience:
- A-Level (or equivalent) ideally in a Science subject
- Quality Control experience would be an advantage and knowledge of Office 2007
- Previous experience as a laboratory Technician in the Chemical industry is essential
As a QC Laboratory Technician, you will be joining a Global Pharmaceutical Organisation who in return are offering a competitive salary.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24399 in all correspondence.
Key words: QC, Quality Control, coatings, glue, compounds, chemical, chemistry jobs, Reena Dhana, London
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| Job Type |
|
Contract |
| Contract Length |
|
0 - 6 months |
| Start Date |
|
|
| Contact Details |
|
|
|
|
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|
|
| Job Title |
|
Process Engineer - Pharmaceutical |
| Salary/rate |
|
£30000 - £40000/annum |
| Location |
|
Newcastle, Wales |
| Job Number |
|
120262037 |
| Posted |
|
25/05/2012 (10:59) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Process Engineer - Pharmaceutical. CK Science are currently seeking to recruit a Process Engineer to work with our client a multi-national pharmaceutical company located near Newcastle.
The successful Process Engineer will be responsible for the pharmaceutical manufacturing processes and unit operations at their manufacturing site.
Ideally, you will qualified in an engineering/sciences discipline and/or have demonstrable working knowledge of engineering processes in a pharmaceutical environment.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference DH24400 in all correspondence.
Keywords: engineering jobs, engineering recruitment, process engineer, chemical engineer, chemical process engineer, chemical engineering jobs, process engineering jobs, engineering jobs north east.
|
| Job Type |
|
Contract |
| Contract Length |
|
6 months + |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Microbiologist - Water, London |
| Salary/rate |
|
£14000 - £18000/annum |
| Location |
|
London |
| Job Number |
|
120262028 |
| Posted |
|
25/05/2012 (10:23) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
CK Science are currently recruiting for a number of Microbiologists to join an Analytical Consulting Laboratory at their site in London on a full time, contract basis.
As a Microbiologist, the main purpose of your role will be:
- Supporting their microbiology team with analysis of water samples.
- Involved in bacterial enumeration, water sampling and testing, endotoxin testing of water samples, media quality control checks, autoclaving and other general support for the laboratory.
As a Microbiologist, you will have the following qualifications, skills and experience:
- BSc in Microbiology (or equivalent)
- Previous experience in a microbiological laboratory is essential
- Experience of water sampling, Crytosporidium sampling or Legionella would be ideal.
- Previous experience in working in a microbiology role in the analytical consulting or related industry is essential.
As a Microbiologist, you will be joining an Analytical Consulting Laboratory who in return are offering a competitive salary.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24395 in all correspondence.
Keywords: London, Microbiology, Microbiologist, Legionella, Water sampling, Water testing
|
| Job Type |
|
Permanent |
| Contract Length |
|
n/a |
| Start Date |
|
|
| Contact Details |
|
|
|
|
|
|
|
| Job Title |
|
Laboratory Assistant - Cambridge |
| Location |
|
Cambridge, Cambridgeshire |
| Job Number |
|
120262023 |
| Posted |
|
25/05/2012 (10:09) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
CK Science are currently recruiting for a Laboratory Assistant to join a Research Group for a pharmaceutical company based in Cambridge on a full time, temmporary basis.
As Laboratory Assistant you will require experience in:
The ability to prepare and sterilise culture media
The removal of waste material from all laboratory areas and place into designated external waste skips
The restocking of laboratory consumable
General washing-up and keeping the area clean at all times
The successful Laboratory Assistant will have the following qualifications, skills & experiences:
A 'Level (or equivalent) in Biology or Chemistry.
Experience in the preparation of solid media in sterile dishes and preparing and providing sterile glassware as and when required.
If successful, you will be joining a global company and in return there is the opportunity to gain experience within a research laboratory which will enable career progression opportunities.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
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. Please quote reference ST24397 in all correspondence.
Keywords: Laboratory Jobs, Laboratory Technician
|
| Job Type |
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Contract |
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0-6 Months |
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| Job Title |
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Laboratory Analyst - Oil & Gas |
| Location |
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Stocktonon Tees, North East |
| Job Number |
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120262022 |
| Posted |
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25/05/2012 (10:01) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Laboratory Analyst - Oil & Gas. CK Science is currently seeking to recruit a number of Laboratory Analysts to work with our client that provides analytical services to the Oil & Gas sector. There are a number of openings for Laboratory Analysts to work a shift basis.
The successful candidate will be responsible for analysing oils and petrochemicals using a range of tests including density, viscosity, COBs and BODs. You will work in a high throughput environment with quick turnaround times.
Ideally, you will be qualified in a science related subject and/or have demonstrable working experience in an analytical testing laboratory.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference DH24387 in all correspondence.
Keywords: science jobs, science recruitment, laboratory analyst, lab analyst, laboratory technician, lab tech, Oil & Gas jobs.
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Contract |
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6 months + |
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Clinical Data Manager |
| Location |
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South East |
| Job Number |
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120262021 |
| Posted |
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25/05/2012 (10:01) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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CK Clinical is currently recruiting for a Clinical Data Manager for a leading Pharmaceutical organisation in the South-East UK.
In this new role as Data Manager, you will help shape a small, growing team in the UK and it will be the perfect environment for your clinical research expertise and your knowledge of EDC. You will be an individual contributor performing complex data management tasks independently and managing external vendors on assigned studies. Besides reviewing clinical study protocols, you will develop eCRFs for new and complex projects, conduct the cross-functional Data Review and develop the Data Management study timeline. Another part of your brief will involve overseeing vendor DM activities, including timeliness and quality of deliverables, and also reviewing statistical tables and listings and Clinical Study Reports, ensuring study compliance with SOPs and regulations. In addition, you will plan and oversee development of Data Management Plans, Data Entry Guidelines, CRF Completion Guidelines, Data Review Guidelines, and eCRF help text; and plan, perform and oversee development of specifications for eCRFs, edit checks, electronic data handling, and manual review.
Interested applicants will hold a degree (OR Equivalent) in a Life Science, Computer Science or other related discipline, and you will have proven experience of working within the Biotechnology/CRO/Pharmaceutical field. You will hold excellent knowledge of Clinical Data Management and EDC (ideally InForm), and have well-developed communication skills to liaise with various stakeholders across the business.
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference CL24392 in all correspondence.
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Permanent |
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n/a |
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Temporary Site QA Lead - W, Midlands |
| Location |
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West Midlands |
| Job Number |
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120262015 |
| Posted |
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25/05/2012 (09:40) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Our Client is looking to recruit a Temporary Site QA Lead for the duration of 9 months.
A Site Quality Leader is responsible for ensuring quality and regulatory compliance of the facility, while driving process effectiveness and efficiency. The Site Quality Leader represents the company to external agencies and champions the evolution of the quality culture for the site.
Key responsibilities include:
• Directing the Site Quality Management System, fully integrated into the Global Quality Management System, including cross-functional and site-specific processes. The role is responsible for facility compliance covering voluntary, regulatory and company quality requirements and will champion quality initiatives at all levels of the organization.
• Maintaining and improving all aspects of Site Quality Planning.
• Overseeing all Quality-related communications and training requirements for all site employees
• Establishing positive relationships with outside agencies.
• Hosting Quality System audits and inspections.
• Overseeing the Corrective Action / Preventive Action activities and Complaint Handling Programs, and in some cases, Quality Engineering.
• Report on Quality System effectiveness and requirements to management team as required including preparing and executing facility Quality Management Reviews.
• Driving the definition of site quality objectives, metrics, reporting and operating mechanisms.
• Participating in selected global initiatives to share best practices and leverage quality synergies.
• Supporting local R&D programs and quality issue resolution.
• Acting as Management Representative for Quality at the Site.
• Operates a Local Inspection program and manages f/up activities to close NCs.
To be considered for this position you will have a Bachelor's degree or equivalent in Engineering, Medical Device Technology or Scientific Field. You will have an understanding of product development, manufacturing, quality control and servicing in the medical equipment or pharmaceutical industry. You will also have hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference SH24376 in all correspondence.
Keywords: science jobs,QA, quality assurance, FDA, QSR, ISO, MDD, temporary
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Contract |
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6 months + |
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ASAP |
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Clinical Manager, Urology |
| Location |
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Buckinghamshire |
| Job Number |
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120262012 |
| Posted |
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25/05/2012 (09:32) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Clinical Manager, Urology
Good daily rate
12 month contract
Home Counties
A one year contract position with an international pharmaceutical company. You will oversee a European Urology study from start up to close out. This will not be a line management role, though you will have team members reporting into you on a matrix basis. You will oversee the development and execution of the clinical study plan, have budgetary responsibility and manage supplies, third party vendors and documentation aspects of the study
Requirements:
Clinical project management experience on an EU or global basis, from start-up to close-out
Urology trial experience would be advantageous
The ideal candidate will also have had experience of trial monitoring
Thorough understanding of ICH-GCP requirements
Ability to travel up to 25%
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference CL24394 in all correspondence.
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Contract |
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6 months + |
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ASAP |
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Senior Medical Writer |
| Location |
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Berkshire |
| Job Number |
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120261935 |
| Posted |
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24/05/2012 (14:44) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Senior Medical Writer
A company in Berkshire are now recruiting for an Office based Senior Medical Writer in Berkshire. This is an opportunity to be part of a team of medical writers and enjoy Medical writing to its extreme.
Main duties and responsibilities:
Ensure that medical writing documents for various projects assigned to the SMW by the Lead Medical Writer (LMW) or Medical Writing Manager (MWM) are prepared according to appropriately rigorous, objective and informative medical writing procedures and processes, and are prepared, reviewed and approved in a quality, timely and accurate manner such that the data presented will withstand examination by regulatory bodies.
Qualifications & Experience
- Life science degree, preferably with a higher degree (MSc or PhD) or other relevant qualifications
- Demonstrated ability to quickly assimilate new variety of therapeutic areas.
- Good understanding of GCP, coupled with prior experience in clinical/preclinical pharmaceutical research and development.
- Good understanding of the clinical development process and of ICH guidelines.
- Significant experience of working on summary level documents such as the Common Technical Document or Investigator's Brochures.
- Capable of demonstrating the capacity to plan effectively and interact satisfactorily with staff of differing disciplines and at all levels of seniority.
- Well developed writing, time management, communication, presentation, analytical and interpersonal skills
- Demonstrable ability to manage complex projects, and coordinate production of multiple documents.
- Demonstrable time management, communication, organisational and interpersonal skills
- Ability to present information in a clear, accurate, logical and non-technical manner
- Ability to plan and prioritise own and other's workload and interact with staff of differing disciplines
- Ability to use initiative to resolve queries and ability to deal with matters confidently and efficiently
- Ability to work within a multidisciplinary team at all levels of seniority, and be pragmatic
- Hardworking with attention to detail
- Responsible, flexible and accountable with a business-focussed pro-active approach
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
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. Please quote reference CL24259 in all correspondence.
Keywords: Senior Medical Writer, Berkshire, ICH guidelines, regulatory authorities, clinical study protocols, remediate gaps
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| Job Type |
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Contract |
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6 months + |
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ASAP |
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