 |
| Job Title |
Senior Immunoassay Scientist - Fordham - 24-30K |
| Salary/rate |
£24000 - £30000/annum Great Package |
| Location |
Cambridge, Cambridgeshire |
| Job Number |
120183829 |
| Posted |
19/03/2010 (17:47) |
| Agency/Employer |
North Point Recruitment Ltd |
Description
|
Senior Clinical Immunoassay Scientist - Fordham - 24-30K
My client is one of the UK's largest CROs, part of a rapidly expanding group of companies they are leaders in the field of drug testing and drug discovery. Currently they are looking for an experienced Immunoassay Scientist to join the team in Fordham, Cambridgeshire.
If you have a relevant life science degree and strong practical experience with immunoassay development in a regulated environment then this is the role for you. Working within the Bioanalytical Science department, the successful candidate will take a lead role in the development, validation and application of quantitative therapeutic biologics and biomarker assays.
Requirements:
+ Life Science Degree
+ Significant work experience within a clinical / analytical laboratory with LIMS reporting is essential as is a working knowledge of GLP/GCP regulations.
+ Demonstrated practical experience of immunoassay techniques including ELISA, RIA, EIA and biomarkers is essential
+ An understanding of drug development processes would be helpful.
+ Previous Study Director / Project Leader and supervisory experience would be advantageous.
This is an opportunity to work with an expanding and progressive company that places emphasis on staff development and training.
If you think the role sounds interesting please contact Stephen Joynes at North Point Recruitment -
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
ASAP |
| Contact Details |
 |
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|
|
| Job Title |
Immunoassay Scientists - Fordham - 17-24K |
| Salary/rate |
£17000 - £24000/annum Great Package |
| Location |
Cambridge, Cambridgeshire |
| Job Number |
120183831 |
| Posted |
19/03/2010 (17:42) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
Immunoassay Scientists - Fordham - 17-24K
My client is one of the UK's largest CROs, part of a rapidly expanding group of companies they are leaders in the field of drug testing and drug discovery. Currently they are looking for a number of Immunoassay Scientists to join the team in Fordham, Cambridgeshire.
If you have a relevant life science degree and strong practical experience with immunoassays then this is the role for you. Successful candidates will be involved with performing assay development and analysis.
Requirements:
+ Life Science Degree
+ 12 months or more work experience within the pharma/biotech industry would be a distinct advantage as would a knowledge of GLP/GMP regulations.
+ Demonstrated practical experience of immunoassay techniques including ELISA, RIA, EIA and biomarkers is essential
+ An understanding of drug development processes would be a distinct advantage.
This is an opportunity to work with an expanding and progressive company that place emphasis on staff development and training. If you think the role sounds interesting please contact Stephen Joynes at North Point Recruitment -
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
ASAP |
| Contact Details |
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|
|
| Job Title |
Client Manager - Biologicals - 35K - Cambridge |
| Salary/rate |
£26000 - £35000/annum Great Package |
| Location |
Cambridge, Cambridgeshire |
| Job Number |
120183827 |
| Posted |
19/03/2010 (17:33) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
Client Manager - Biologicals - 35K - Cambridge
My client is one of the UK's largest CROs, part of a rapidly expanding group of companies they are leaders in the field of drug testing and drug discovery. Currently they are looking for an experienced Immunoassay Scientist to join the team in Fordham, Cambridgeshire.
The ideal candidate for this role will have a science based qualification and will be an experienced Immunoassay development scientist with experience using the LIMS system. Also experience working as a manager or a team leader is essential as the role includes managing a team of scientists.
This role will also involve the building of relationships with clients and some project management.
Ideally the suitable candidate will have several years experience working within a similar role.
If you are looking for a new challenge this may be the position for you.
The package will include
33-38K Basic
25 days holiday entitlement
Pension scheme
If you like what this role has to offer please contact Stephen Joynes at or call on 0870 444 5644
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
ASAP |
| Contact Details |
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|
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| Job Title |
Shift Process Chemist - Dorset |
| Salary/rate |
£30000 - £43000/annum benefits and relocation assistance |
| Location |
Dorset, Dorset |
| Job Number |
120183459 |
| Posted |
16/03/2010 (16:34) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
My client is the world's largest supplier of Chemicals, to Commercial, Government and Academic establishments. Due to ongoing expansion, they are currently recruiting for experienced Process Chemists to join their R&D team, on a shift basis. The position will be based at their cGMP site in Dorset. Please take a look at the advertisements below and let us know if you wish to be considered.
You will provide the production shift teams with any necessary technical and operational support in the manufacture of bulk fine chemicals to the Production Schedule and within all regulatory requirements and my clients standards and procedures.
60% Plant
30% Office
10% Lab
Your duties will include:
Closely monitoring all processes on plant by collection of data, observation, coaching of operators, analysis of key process streams and where appropriate generation of mass balance for key materials.
Speedy investigation into the causes of processing problems and deviations on plant and implement corrective and preventative measures.
Generation of manufacturing reports for custom projects.
Deputising for the Shift Leader as required by their absence through holidays, sickness or other company business that prevents them from performing their critical duties
Implementing learning from campaigns through rewriting of batch records.
Generation of PCC and additional processing instructions to resolve issues on plant.
Completing hand-over of process related problems and documentation issues to the oncoming shift chemist.
Supporting the development group with out of hours lab work when agreed in advance.
Operating processing equipment in the manufacture of cGMP chemical products in compliance with internal procedures and the Company's Health, Safety and Environment policy. This is only in the event of severe manpower shortage.
Working closely with Development Chemists, the Shift Leader, Operators and Production Management and external customers, it is essential that you are qualified with a BSc in Chemistry (a PHD in Chemistry would be desirable), possess thorough and logical problem solving skills together with Risk Assessment and Process Improvement skills. You will need to be computer literate, especially with Project and Excel. It is desirable that you have an understanding of Word, Powerpoint and IPPC, Practical GMP, basic engineering regulations and principles.
Self critical with a determination to find root causes, you will need to be a good technical communicator capable of converting complex processes into understandable language for operators. You should have good practical GMP knowledge, a thorough understanding of Safety requirements and Risk Assessment procedures for chemical manufacturing at scale. You must also have a good knowledge of Environmental compliance and reporting requirements under IPPC legislation.
Salary: £30,000 - £35,000 + Shift Allowance (£7373), benefits and relocation assistance.
To be considered for this role, please send your updated CV and covering letter to:
Brendan Rogers at North Point Recruitment.
All applicants must be eligible to work within the UK.
North Point Recruitment is acting as a recruitment consultancy in relation to this position.
|
| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
16/03/2010 |
| Contact Details |
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|
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| Job Title |
Microbiology Section Head - Pharmaceuticals - Cambridge - 16-20 |
| Salary/rate |
£16000 - £20000/annum Great Package |
| Location |
Cambridge, Cambridgeshire |
| Job Number |
120183456 |
| Posted |
16/03/2010 (16:31) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
Microbiology Section Head - Pharmaceuticals - Cambridge - 16-20K
Key Skills - UKAS - Microbiology
Based in Ashford a fantastic opportunity has arisen for an experienced Microbiologist to work with one of the UK's leading independent analysis and consultancy service providers in the food, dairy, pharmaceutical, water and environmental sectors.
If you are an experienced Microbiologist with proven supervisory skills then this is the role for you. As Section Head of the Pharmaceutical Section you will be responsible for the day-to-day supervision and organisation of the pharmaceutical section to ensure that all samples are analysed within timescales.
Role Requirements:
+ Degree in Microbiology
+ Previous supervisory experience is essential
+ Specific knowledge and experience of methods for the analysis of pharmaceutical
Benefits:
+ Starting salaries in the 16-20K range. Salaries are flexible for the right candidate.
+ Good pension with 5% matched by the client
+ Flexible working hours
+ Solid career path
+ Extensive training in new aspects of the Microbiology field
If this role sounds interesting please contact Stephen Joynes at North Point Recruitment on 0870 444 5644 -
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
ASAP |
| Contact Details |
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|
|
|
|
| Job Title |
Senior Project Manager - York - 28-32K |
| Salary/rate |
£30000 - £32000/annum Great Package |
| Location |
York, North Yorkshire |
| Job Number |
120183332 |
| Posted |
15/03/2010 (15:58) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
Clinical Project Manager - York - 32K
My client specializes in laboratory science and clinical research, conducting clinical trials across the globe with operations that extend to more than 60 countries. Due to continuing success they are currently looking for a Project Manager to join the team in York.
This role would suit someone with significant clinical trials experience, maybe a CRA or CTA looking to take that next step on the career ladder. The successful candidate will provide project management services for clients throughout the entire study life cycle.
The ideal candidate will have:
+ BSc in a relevant subject
+ Proven experience working on clinical trials
+ Working knowledge of ICH guidelines for Good Clinical Practice
+ Excellent organisational and communication skills are essential for this role
If you think this role sounds interesting please contact Stephen Joynes at North Point Recruitment -
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
ASAP |
| Contact Details |
|
|
|
|
|
| Job Title |
Awesome Quality Assurance/Regulatory Affairs Manager |
| Salary/rate |
£30000 - £40000/annum Benefits |
| Location |
Bristol, South West |
| Job Number |
120183262 |
| Posted |
14/03/2010 (13:01) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
This is a brilliant opportunity for the position of
Medical Devices QARA Manager- South East (Wiltshire) 30-40K Negotiable April-May Start.
The Position is Based in Wiltshire commutable from Bristol and eastern end of AVON or M4 corridor towards Swindon
My client is a highly reputed and a well established business associated with Medical Devices sector. An ISO accredited site they work to ISO13485 regulations and currently their products are being marketed in The UK and in The US.
Managing a team of QA, RA and HSE staff the position requires excellent management, planning, communication, decision making and interpersonal skills. With experience in the relevant sector particularly from the Medical Devices Sector the successful applicant will be required to lead a team of QA/RA Function across site and other relevant staff such as HSE Advisor
Ideally educated to a Scientific or an Engineering degree you will be competent to demonstrate your “Direct Experience gained by responsibilities” in the following competencies:
QA Systems Bias: Quality Management Systems Implementation, Revamp, Improvement, conducting QA Audits and ensuring compliance to ISO13485
QA Manufacturing Bias: Documentation, Processes, CAPAs, Investigations and closing out OOS and other associated non-conformances to ISO 13485
Regulatory Affairs: With experience in CE Marking of Devices, 510(k) Submissions, familiarity and perhaps experienced in US FDA markets, EU MDD’s as 93/42 etc is desirable
HSE: Some experience in Health and Safety issues in relevant sector would be desirable.
The competent person would have ideally 3-4 years or more experience of managing Quality Assurance staff preferably from Medical Devices sector. Ideally you will be a existing QARAManager or a Senior QARA Officer with supervision experience in a Medical Device business through current role.
The position will report to Senior Operations Management
If this position is of interest please do not hesitate to contact Rakesh at North Point. I would however require your CV before hand to be able to discuss the position further.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
11/03/2010 |
| Contact Details |
|
|
|
|
|
| Job Title |
Fantastic position Quality Assurance/Regulatory Affairs Manager |
| Salary/rate |
£30000 - £40000/annum Benefits |
| Location |
Swindon, Wiltshire |
| Job Number |
120183260 |
| Posted |
14/03/2010 (10:01) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
This is a brilliant opportunity for the position of
Medical Devices QARA Manager- South East (Wiltshire) 30-40K Negotiable April-May Start.
The Position is Based in Wiltshire commutable from most places on M4 Corridor, Southern End of Oxfordshire and for anyone who can commute to Swindon or surrounding area daily.
My client is a highly reputed and a well established business associated with Medical Devices sector. An ISO accredited site they work to ISO13485 regulations and currently their products are being marketed in The UK and in The US.
Managing a team of QA, RA and HSE staff the position requires excellent management, planning, communication, decision making and interpersonal skills. With experience in the relevant sector particularly from the Medical Devices Sector the successful applicant will be required to lead a team of QA/RA Function across site and other relevant staff such as HSE Advisor
Ideally educated to a Scientific or an Engineering degree you will be competent to demonstrate your “Direct Experience gained by responsibilities” in the following competencies:
QA Systems Bias: Quality Management Systems Implementation, Revamp, Improvement, conducting QA Audits and ensuring compliance to ISO13485
QA Manufacturing Bias: Documentation, Processes, CAPAs, Investigations and closing out OOS and other associated non-conformances to ISO 13485
Regulatory Affairs: With experience in CE Marking of Devices, 510(k) Submissions, familiarity and perhaps experienced in US FDA markets, EU MDD’s as 93/42 etc is desirable
HSE: Some experience in Health and Safety issues in relevant sector would be desirable.
The competent person would have ideally 3-4 years or more experience of managing Quality Assurance staff preferably from Medical Devices sector. Ideally you will be a existing QARAManager or a Senior QARA Officer with supervision experience in a Medical Device business through current role.
The position will report to Senior Operations Management
If this position is of interest please do not hesitate to contact Rakesh at North Point. I would however require your CV before hand to be able to discuss the position further.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
11/03/2010 |
| Contact Details |
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|
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| Job Title |
Quality Control Chemists - South West |
| Salary/rate |
£30000/annum benefits and relocation |
| Location |
South West England, South West |
| Job Number |
120183168 |
| Posted |
12/03/2010 (12:58) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
My client is the world's largest supplier of Chemicals to Commercial, Government and Accademic establishments. Due to ongoing expansion, they are currently recruiting for experienced Quality Control Analysts to join their team of analytical chemists. The position will be based at their cGMP Gillingham site in Dorset.
The position will involve the routine testing of APIs using an array of analytical techniques (HPLC, GC, NMR, ICP, Ion Chromatography and classic techniques). Validation of analytical methods, as well as using current analytical and chromatography data systems.
Successful candidates for this position will be educated to at least degree standard in a Chemistry related subject. Significant experience of testing a variety of pharmaceutical products using a broad range of techniques; such as HPLC, GC, NMR, ICP and Ion Chromatography. Experience of validating analytical methods, ideally in a quality control department. Experience of working to cGMP standard, and working in a FDA environment would be an advantage.
Salary: Flexible + Benefits and relocation allowance
If you wish to be considered for this position, forward your CV to:
Brendan Rogers at North Point Recruitment.
All applicants must be eligible to work within the UK.
North Point Recruitment is acting as a recruitment business in relation to this position.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
01/03/2010 |
| Contact Details |
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|
|
| Job Title |
MEDICAL WRITING COMMUNICATION- SPECIALIST |
| Salary/rate |
£22000 - £40000/annum Benefits |
| Location |
Greater Manchester, Greater Manchester |
| Job Number |
120180547 |
| Posted |
11/03/2010 (15:29) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
Our client is one of the most successful, inspiring and a leading Medical Communications Consultancy/Agency offering and providing services to health and medical sectors. Based in North West of England (Southern Part of Greater Manchester) they are a highly dynamic, ambitious and a warm team to work with.
MEDICAL WRITERS OR
SENIOR MEDICAL WRITERS
AND
EDITORIAL SPECIALIST OR
SENIOR MEDICAL EDITORIAL SPECIALIST
OFFICE BASED FULL TIME PERMANENT POSITION's ARE BASED IN THE NORTH WEST OF ENGLAND
Commutable from Sheffield, Stockport, Manchester, Greater Manchester, Warrington, Parts of Derbyshire, Huddersfield, Macclesfield, Chester.
As a part of this expansion my client would love to hear from highly dynamic and success driven individuals with experience in fields of Cardiovasculars, Neurology or Oncology or similar segments within Medical Journalism.
Effectively there are two roles Medical Writer and Editorial Specialist. Depending of the breadth of experience the applicant will offer the position would then be determined based on merits and credits.
The Editorial position will certainly require the applicant to possess relevant management, training, mentoring, supervision and coaching skills as well as skills related to Medical Writing particularly with competencies in Editing.
For any additional information please feel free to contact me at North Point recruitment 01612368200.
Please ask for Rakesh
|
| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
19/02/2010 |
| Contact Details |
|
|
|
|
|
| Job Title |
Fantastic position Quality Assurance/Regulatory Affairs Manager |
| Salary/rate |
£30000 - £40000/annum Benefits |
| Location |
Swindon, Wiltshire |
| Job Number |
120183058 |
| Posted |
11/03/2010 (14:55) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
This is a brilliant opportunity for the position of
Medical Devices QARA Manager- South East (Wiltshire) 30-40K Negotiable April-May Start.
The Position is Based in Wiltshire commutable from most places on M4 Corridor, Southern End of Oxfordshire and for anyone who can commute to Swindon or surrounding area daily.
My client is a highly reputed and a well established business associated with Medical Devices sector. An ISO accredited site they work to ISO13485 regulations and currently their products are being marketed in The UK and in The US.
Managing a team of QA, RA and HSE staff the position requires excellent management, planning, communication, decision making and interpersonal skills. With experience in the relevant sector particularly from the Medical Devices Sector the successful applicant will be required to lead a team of QA/RA Function across site and other relevant staff such as HSE Advisor
Ideally educated to a Scientific or an Engineering degree you will be competent to demonstrate your “Direct Experience gained by responsibilities” in the following competencies:
QA Systems Bias: Quality Management Systems Implementation, Revamp, Improvement, conducting QA Audits and ensuring compliance to ISO13485
QA Manufacturing Bias: Documentation, Processes, CAPAs, Investigations and closing out OOS and other associated non-conformances to ISO 13485
Regulatory Affairs: With experience in CE Marking of Devices, 510(k) Submissions, familiarity and perhaps experienced in US FDA markets, EU MDD’s as 93/42 etc is desirable
HSE: Some experience in Health and Safety issues in relevant sector would be desirable.
The competent person would have ideally 3-4 years or more experience of managing Quality Assurance staff preferably from Medical Devices sector. Ideally you will be a existing QARAManager or a Senior QARA Officer with supervision experience in a Medical Device business through current role.
The position will report to Senior Operations Management
If this position is of interest please do not hesitate to contact Rakesh at North Point. I would however require your CV before hand to be able to discuss the position further.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
11/03/2010 |
| Contact Details |
|
|
|
|
|
| Job Title |
Awesome Quality Assurance/Regulatory Affairs Manager |
| Salary/rate |
£30000 - £40000/annum Benefits |
| Location |
Bristol, South West |
| Job Number |
120183053 |
| Posted |
11/03/2010 (14:49) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
This is a brilliant opportunity for the position of
Medical Devices QARA Manager- South East (Wiltshire) 30-40K Negotiable April-May Start.
The Position is Based in Wiltshire commutable from Bristol and eastern end of AVON or M4 corridor towards Swindon
My client is a highly reputed and a well established business associated with Medical Devices sector. An ISO accredited site they work to ISO13485 regulations and currently their products are being marketed in The UK and in The US.
Managing a team of QA, RA and HSE staff the position requires excellent management, planning, communication, decision making and interpersonal skills. With experience in the relevant sector particularly from the Medical Devices Sector the successful applicant will be required to lead a team of QA/RA Function across site and other relevant staff such as HSE Advisor
Ideally educated to a Scientific or an Engineering degree you will be competent to demonstrate your “Direct Experience gained by responsibilities” in the following competencies:
QA Systems Bias: Quality Management Systems Implementation, Revamp, Improvement, conducting QA Audits and ensuring compliance to ISO13485
QA Manufacturing Bias: Documentation, Processes, CAPAs, Investigations and closing out OOS and other associated non-conformances to ISO 13485
Regulatory Affairs: With experience in CE Marking of Devices, 510(k) Submissions, familiarity and perhaps experienced in US FDA markets, EU MDD’s as 93/42 etc is desirable
HSE: Some experience in Health and Safety issues in relevant sector would be desirable.
The competent person would have ideally 3-4 years or more experience of managing Quality Assurance staff preferably from Medical Devices sector. Ideally you will be a existing QARAManager or a Senior QARA Officer with supervision experience in a Medical Device business through current role.
The position will report to Senior Operations Management
If this position is of interest please do not hesitate to contact Rakesh at North Point. I would however require your CV before hand to be able to discuss the position further.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
11/03/2010 |
| Contact Details |
|
|
|
|
|
| Job Title |
Awesome Quality Assurance/Regulatory Affairs Manager |
| Salary/rate |
£30000 - £40000/annum Benefits |
| Location |
Oxfordshire, Oxfordshire |
| Job Number |
120183051 |
| Posted |
11/03/2010 (14:43) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
QARA Manager- South East (Wiltshire) 30-40K Negotiable April-May Start.
The Position is Based in Wiltshire commutable from Southern end of Oxfordshire.
My client is a highly reputed and a well established business associated with Medical Devices sector. An ISO accredited site they work to ISO13485 regulations and currently their products are being marketed in The UK and in The US.
Managing a team of QA, RA and HSE staff the position requires excellent management, planning, communication, decision making and interpersonal skills. With experience in the relevant sector particularly from the Medical Devices Sector the successful applicant will be required to lead a team of QA/RA Function across site and other relevant staff such as HSE Advisor
Ideally educated to a Scientific or an Engineering degree you will be competent to demonstrate your “Direct Experience gained by responsibilities” in the following competencies:
QA Systems Bias: Quality Management Systems Implementation, Revamp, Improvement, conducting QA Audits and ensuring compliance to ISO13485
QA Manufacturing Bias: Documentation, Processes, CAPAs, Investigations and closing out OOS and other associated non-conformances to ISO 13485
Regulatory Affairs: With experience in CE Marking of Devices, 510(k) Submissions, familiarity and perhaps experienced in US FDA markets, EU MDD’s as 93/42 etc is desirable
HSE: Some experience in Health and Safety issues in relevant sector would be desirable.
The competent person would have ideally 3-4 years or more experience of managing Quality Assurance staff preferably from Medical Devices sector. Ideally you will be a existing QARAManager or a Senior QARA Officer with supervision experience in a Medical Device business through current role.
The position will report to Senior Operations Management
If this position is of interest please do not hesitate to contact Rakesh at North Point. I would however require your CV before hand to be able to discuss the position further.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
11/03/2010 |
| Contact Details |
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|
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|
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| Job Title |
Process Development / Validation Chemist - Medical Devices |
| Salary/rate |
£25000 - £40000/annum |
| Location |
Wiltshire, Wiltshire |
| Job Number |
120182879 |
| Posted |
10/03/2010 (10:02) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
My client is a leader in Research, Development and Manufacture of advanced wound care dressings (class 1,2 and 3 medical devices). Specialising in gel adhesives. Due to new projects moving to manufacture, my client is looking for a process development chemist or validation engineer, with a solid understanding of validating class 3 medical device manufacturing processes.
The role will fundamentally involve validating manufacturing processes for a new drug delivery product (class 3). This will involve process and equipment validation, requiring a good regulatory and quality knowledge (GMP and FDA).
Ideally candidates will come from a chemical / wound care background, with a solid understanding of the requirements of validating processes, and equipment for GMP manufacture of class 3 medical devices to FDA regulations
This opportunity is initially a 6 month contract, with the possibility of extension or permanent placement.
Salary: Flexible, depending on experience.
To be considered for this position, please forward your CV to:
Brendan Rogers at North Point Recruitment.
All applicants must be eligible to work within the UK.
North Point Recruitment is acting as a recruitment business in relation to this position
|
| Job Type |
Contract |
| Contract Length |
Permanent |
| Start Date |
10/03/2010 |
| Contact Details |
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|
|
| Job Title |
**Water Jet Cutting Engineer** |
| Salary/rate |
£20000 - £30000/annum |
| Location |
Milton Keynes, Buckinghamshire |
| Job Number |
107500698 |
| Posted |
02/03/2010 (09:11) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
My client is one the leading organisations in their field. They allow pipes to be joined without the need for flanging, grooving, threading or welding.
The company boasts an impressive market share with sales in over 160 countries as well as an ever-expanding product range and continued investment throughout the organisation.
An excellent opportunity has arisen for a Water Jet Cutting Engineer to join this ever expanding company.
The potential within this role is really impressive: The company offers great prospects for progression and career development and also a good salary and benefits package as well.
If you feel that you have the right background and the right attitude to take you career further within a respected and renowned company, send your CV over to Jack at North Point Recruitment today on or call 0161 236 8200
|
| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
02/02/2010 |
| Contact Details |
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|
|
|
| Job Title |
Formulation Development Scientist (food/pharma) |
| Salary/rate |
£30000 - £50000/annum negotiable |
| Location |
Liverpool, Merseyside |
| Job Number |
120181508 |
| Posted |
25/02/2010 (17:06) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
|
My Client specialises in the discovery, development and Licensing of new Functional Food, Medical Food and Dietary Supplement technologies. Working hand in hand with premier international research institutes, and commercialising new technology with leading brand owners. Due to the opening of a new site in the North-West, my client is looking to recruit an experienced Formulation Scientist.
This position will involve heading up the Formulation Development of food and/or liquid extracts, working along side other principal scientists in developing a range of bioactive laboratory extracts into standardised industrial products.. Aiding in delivering new technologies to commercialisation, through scale up, and pilot plant development. Other duties will include aiding in designing and outfitting a suitable laboratory, used mainly for analytical and formulation development; also including pilot scale facilities for initial small scale formulation development.
The successful candidate will be of graduate calibre, with a strong background in and industrial formulation role; ideally within the food or botanical extracts industry. Experience of project management / laboratory management is preferred; spanning different product types. A thorough knowledge of common industrial-scale processes and equipment is also required. Experience of interpretation of analytical work, with techniques such as HPLC, GC, MS would be desired, as well as experience of working within GLP standards.
Salary: Generous, depending on experience
To be considered for this position, please forward your CV to:
Brendan Rogers at North Point Recruitment (0161 236 8200).
North Point Recruitment is acting as a recruitment business in relation to this position.
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
16/02/2010 |
| Contact Details |
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|
|
| Job Title |
**Service Engineer - London** |
| Salary/rate |
£25000 - £28000/annum |
| Location |
London, London |
| Job Number |
107506880 |
| Posted |
25/02/2010 (09:00) |
| Agency/Employer |
North Point Recruitment Ltd |
| Description
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Service Engineer - London
· Highly Competitive Salary - Circa £25-28k
· Immediate Start Available
· Excellent Working Environment
· Good Opportunity for further managerial development
The Company
My client provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing and metrology, to a broad range of scientific R&D and QC measurements.
They boast an impressive list of customers and through a commitment to ensuring an efficient and high quality service; the company has enjoyed continued growth and a growing reputation in this field.
The Opportunity
An exciting opportunity has arisen for a Service Engineer with a strong technical and hands-on background with ideally experience in servicing scientific / analytical instruments.
The position will be based in London but extensive UK travel is anticipated.
Ideally you will have experience on the following instruments: Raman, Fluorescence, Lasers and Particle Size Analysers.
This is a good opportunity within a workplace that offers fantastic rewards, incentives and ongoing investment and support to its valued workforce.
If you believe that you have the right experience and expertise required for this role and that you are also looking for a new and challenging role within your career, send your CV over to Jack Bowen at North Point Recruitment as soon as possible on or call 0161 236 8200
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| Job Type |
Permanent |
| Contract Length |
Permanent |
| Start Date |
27/01/2010 |
| Contact Details |
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