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| Job Title |
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European Marketing Manager Oncology & Virology - £70k |
| Salary/rate |
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£65000 - £70000/annum £7k car allowance, 15% bonus, pensio |
| Location |
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England, UK |
| Job Number |
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129157205 |
| Posted |
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22/02/2012 (16:44) |
| Agency/Employer |
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Cranleigh Group |
Description
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European Marketing Manager - Virology/Oncology - Can be based in the UK, France or Germany, to £70k + Excellent Benefits
We are currently seeking an experienced Marketing Manager to join a global molecular diagnostics company, during an exciting period of growth.
The purpose of this role is to lead the European organisation in the marketing and product management of the Virology and Oncology portfolio.
Accountabilities
* Market and manage the Virology and Oncology products for the Region, driving the successful launch of new Virology and Oncology tests and leading the development of the European Virology and Oncology market to achieve budget for all associated products
* Manage budget and forecast for associated products
* Prepare and implement a European marketing plan for all associated products
* Deliver monthly reports, and quarterly marketing plan updates
* Develop and communicate key messages, value propositions, marketing programmes, and sales tools for associated products
* Train sales force on optimal usage of marketing and sales tools
* Regularly travel with sales representatives on sales calls to understand customer issues and front line challenges to successful selling of associated products, coach on how to best implement and overcome challenges, develop sales tools and program to address these needs. Provide feedback to sales and marketing on visits.
* Develop and maintain an excellent relationship with global and country marketing teams as well as Distributors, coordinating activities with all key stakeholders
* Ensure there is a high level of awareness of market developments, government policies, competitor activities and customer's needs.
* Promotes meetings and initiatives with Key Opinion Leaders, taking opportunities for leveraging Product Portfolio.
* Work on Distribution Channel Strategies.
Experience, qualifications, skills required:
* Progressive sales and/or product/marketing management experience, with a background in healthcare. Must have a proven track record that clearly demonstrates success in sales and marketing positions with increasing levels of responsibility.
* Experience in the disease area and knowledge of real time PCR reagents and instruments is desired
* Because of the technical nature of the products, an understanding of the assigned products and their relationship to diagnostic and clinical medicine is essential. Must possess a high degree of sensitivity and maintain close contact with the marketplace to determine those areas where new clinical diagnostic products with improvements are required.
Preferred Qualifications
* Academic degree in Science.
Other Requirements:
* The candidate must be willing to travel up to 60%.
* The candidate must be perfectly fluent and at ease in oral and written English. Fluency in other languages, e.g. French, German or Spanish is a plus.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Technical Manager-Healthcare-Product Development-Dorset £40-45K |
| Salary/rate |
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£40000 - £45000/annum company car |
| Location |
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Dorset |
| Job Number |
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120251767 |
| Posted |
|
22/02/2012 (16:31) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Technical Manager - Oral and Healthcare Products - Product Development, QC-Dorset £40-£45K
Key Responsibilities:
As Technical Manager your responsibilities for all hardline products will include:
*Main point of contact for all customers regarding technical issues
*Quality assurance - strong links with the factory compliance team & customer ETI and quality audit
Quality control - strong links with quality inspectors
*NPD - strong links with commercial teams
*Product Innovation - with customers, UK commercial & external partners
*Product performance testing and standard setting
*Lean manufacturing
*Developing skills and capabilities with the Far East technical team. This will include time spent with the team in China
*Major input to packaging development for both hardline and formulated products
*Best cost, fit for purpose and best for the environment
*Strong links with far east merchandisers and environmental manager
*Specific focus on toothbrush (manual & electrical) and oral care accessory development
*To be second in command from a technical perspective and where necessary, (during absence/planned leave etc), take on the role of group technical manager
To succeed in this role you will be a graduate with a Degree in Materials Science, Polymer Science or similar together with a background in constructed product development and product QC procedures. Previous experience of working for an independent test organisation would be a distinct advantage as would customer-facing skills, ideally from the retail industry. Someone who is ambitious who wants to learn and progress within the company and able to build customer relationships.
Candidates must be willing to travel both within the UK and to factories in Asia.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Field Service Engineer – Molecular Diagnostics – Based F |
| Salary/rate |
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£29158/annum car allowance, pension, 15% bonus |
| Location |
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France, Non UK |
| Job Number |
|
112157862 |
| Posted |
|
21/02/2012 (19:19) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Field Service Engineer - Molecular Diagnostics - Based France - to 35k euros + benefits
We are seeking an experienced Field Service Engineer to support customers in France for a leading scientific instrumentation company.
Accountabilities
* Travel throughout France and sometimes to other European Countries on short notice to support the company's products and field service partners
* Manage installations and customer training.
* Provide support on company product instrumentation.
* Perform routine standard procedures to isolate and fix problems in malfunctioning equipment or software
* Work closely with the Technical support team to address customer complaints to determine corrective action and customer follow-up
* Document and report the company's product "design reliability" and "maintenance issues" and/or problems to technical support. .
* Able work on-call on designated weekends to provide service support within a short period of time.
* Achieve and exceed Customer Satisfaction objectives
Experience, qualifications, skills required:
* Bachelor's Degree in Electronics or an Engineering related discipline required.
* Experience in field service required.
* Experience with computer hardware and software is essential.
* Prior experience of providing hardware and software improvement feedback, lifecycle maintenance, sales support, and technical services preferred.
* Capable of handling advanced complaints, troubleshooting, and knowledge of GMP & ISO requirements is essential.
* Requires excellent systematic troubleshooting skills utilizing a structured and comprehensive process to determine the root cause and implement corrective action.
* Troubleshooting skills with automation robotics preferred.
* Capable of explaining technical procedures in writing or verbally is essential.
* Possess the ability to work with customers and vendors at both a business & technical level.
* Time management skill with the ability to multi-task and prioritize events and maintain composure under high levels of demand is necessary.
* Ability to work independently with limited supervision is essential.
* Proficient in reporting activities, maintaining local spare parts inventory recording, and travel expenses is necessary.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Field Service Engineer – Molecular Diagnostics – Based G |
| Salary/rate |
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£33324/annum car allowance, pension, 15% bonus |
| Location |
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Germany, Non UK |
| Job Number |
|
112157861 |
| Posted |
|
21/02/2012 (19:15) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Field Service Engineer - Molecular Diagnostics - Based Germany - to 40k euros + benefits
We are seeking an experienced Field Service Engineer to support customers in Germany for a leading scientific instrumentation company.
Accountabilities
* Travel throughout Germany and sometimes to other European Countries on short notice to support the company's products and field service partners
* Manage installations and customer training.
* Provide support on company product instrumentation.
* Perform routine standard procedures to isolate and fix problems in malfunctioning equipment or software
* Work closely with the Technical support team to address customer complaints to determine corrective action and customer follow-up
* Document and report the company's product "design reliability" and "maintenance issues" and/or problems to technical support. .
* Able work on-call on designated weekends to provide service support within a short period of time.
* Achieve and exceed Customer Satisfaction objectives
Experience, qualifications, skills required:
* Bachelor's Degree in Electronics or an Engineering related discipline required.
* Experience in field service required.
* Experience with computer hardware and software is essential.
* Prior experience of providing hardware and software improvement feedback, lifecycle maintenance, sales support, and technical services preferred.
* Capable of handling advanced complaints, troubleshooting, and knowledge of GMP & ISO requirements is essential.
* Requires excellent systematic troubleshooting skills utilizing a structured and comprehensive process to determine the root cause and implement corrective action.
* Troubleshooting skills with automation robotics preferred.
* Capable of explaining technical procedures in writing or verbally is essential.
* Possess the ability to work with customers and vendors at both a business & technical level.
* Time management skill with the ability to multi-task and prioritize events and maintain composure under high levels of demand is necessary.
* Ability to work independently with limited supervision is essential.
* Proficient in reporting activities, maintaining local spare parts inventory recording, and travel expenses is necessary.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Scientific Technical Support Specialist – Molecular Diagnostics |
| Salary/rate |
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£29158 - £33324/annum car allowance, pension, 15% bonus |
| Location |
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France, Non UK |
| Job Number |
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120251615 |
| Posted |
|
21/02/2012 (18:56) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Scientific Technical Support Specialist - Molecular Diagnostics - Based France - to 35k euros + benefits
We are seeking a Field-based Technical Support Specialist for a molecular diagnostics company to support customers in France.
Job Purpose
* Provide customer training on installation of systems and deliver follow up and technical support to customers and the sales organisation
Accountabilities
* Assist and support the Sales team with pre- and post- sale technical activities with a primary emphasis on growing the user base of diagnostic products as rapidly as possible.
* Install instrumentation, train customers and ensure a smooth and rapid start-up for new customers.
* Provide technical direction and technical support to customers on instrument operation, assay process, and maintenance of company products.
* Implement detailed customer start-up requirements related to both products and customer-specific requirements.
* Work closely with sales and marketing to address customer concerns,
* Work closely with tech support to address customer complaints to determine corrective action and customer follow-up.
* Integrate instruments into customer laboratories and provide support to the customer during the evaluation and validation process of the assays
Experience, qualifications, skills required:
* Masters Degree in Biology with experience in Molecular Biology
* Clinical Laboratory focus along with experience in molecular and microbiology techniques
* Results driven and self-motivated with a demonstrated ability achieve measurable goals
* Knowledge of diagnostic market
* Ideally previous technical support/sales experience
* Excellent technical presentation skills for group and one-on-one presentations
* Integrates with the sales team in planning and executing account strategies
* Networks with the scientific community to grow the business
Applicants should be native French, ideally with English language skills.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Technical Support Specialist - Molecular Diagnostics - Germany |
| Salary/rate |
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£37489 - £41655/annum 15% bonus, pension, car allowance |
| Location |
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Germany, Non UK |
| Job Number |
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120251613 |
| Posted |
|
21/02/2012 (18:46) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Scientific Technical Support Specialist - Molecular Diagnostics - Based Germany - to 45k euros + benefits
We are seeking a Field-based Technical Support Specialist for a molecular diagnostics company to support customers in Germany.
Job Purpose
* Provide customer training on installation of systems and deliver follow up and technical support to customers and the sales organisation
Accountabilities
* Assist and support the Sales team with pre- and post- sale technical activities with a primary emphasis on growing the user base of diagnostic products as rapidly as possible.
* Install instrumentation, train customers and ensure a smooth and rapid start-up for new customers.
* Provide technical direction and technical support to customers on instrument operation, assay process, and maintenance of company products.
* Implement detailed customer start-up requirements related to both products and customer-specific requirements.
* Work closely with sales and marketing to address customer concerns,
* Work closely with tech support to address customer complaints to determine corrective action and customer follow-up.
* Integrate instruments into customer laboratories and provide support to the customer during the evaluation and validation process of the assays
Experience, qualifications, skills required:
* Masters Degree in Biology with experience in Molecular Biology
* Clinical Laboratory focus along with experience in molecular and microbiology techniques
* Results driven and self-motivated with a demonstrated ability achieve measurable goals
* Knowledge of diagnostic market
* Ideally previous technical support/sales experience
* Excellent technical presentation skills for group and one-on-one presentations
* Integrates with the sales team in planning and executing account strategies
* Networks with the scientific community to grow the business
Applicants should be native Germans, ideally with English language skills.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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QA Systems Specialist (QMS)-CAPA-Documentation-GMP-Kent-£26-32k |
| Salary/rate |
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£26000 - £32000/annum Benefits (Incl. final salary pension |
| Location |
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Dartford, Kent |
| Job Number |
|
120251483 |
| Posted |
|
21/02/2012 (11:58) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Quality (QA) Systems Specialist - CAPA - GMP - Documentation Review - Diagnostics - Biotechnology - Audits - ISO 13485 - Kent - £26-32k + Excellent Benefits (Incl. final salary pension)
An international Biotechnology company currently require an experienced Quality Assurance (QA) Systems Specialist to join their Quality Division at their site in Dartford, Kent. This is a pivotal role within the group and you will be tasked with supporting the company QMS (Quality Management System).
Your overall focus will be the oversight and monitoring of the Quality System and it's measurements to ensure it is effective and efficient. You will also work as an external and internal audit escort and generalist and aid successful audit/ inspection outcomes.
Duties:
The management of the Quality System Performance Review process and Management Review process, including preparation of the package, chairing of the meetings, preparation of minutes and documentation and tracking of action items.
Reporting Quality System performance metrics to the Quality Manager and Division.
Initiate and manage system level investigations for overall Quality System issues as required.
Ensure compliance to relevant external (Regulatory) requirements as communicated by the Quality Manager including Quality Management System (ISO, EN) , Code of Federal Regulations (CFR) and the Division Quality System.
Co-ordinate external and internal audits/inspections. Escort auditors at all times, work as a generalist to answer their high level questions and gain access to SMEs as required. Be able to act as a Staging Room Manager during external audits.
Track all internal and external audit CAPAs to completion and manage audit documentation according to Q17.01 and Q17.08.
Conduct Quality System Induction Training for new starters and prepare and deliver GMP Refreshers as appropriate.
Be responsible for the health and safety of staff and visitors, including contractors, within the areas supervised and for ensuring that the environment is not adversely affected by the activities of the employees and visitors who they are responsible for.
Organise, chair and take actions from the site Project Portfolio meetings to track projects and Quality Plan items.
Track the Quality Plan to completion.
Manage site Key Performance Indicators and ensure they are up to date and reviewed / communicated regularly.
To be considered for this opportunity you will need to possess first class communication and verbal skills coupled with demonstrable QMS expertise gained ideally within the Biotechnology / Diagnostics or Pharmaceutical sector. Excellent I.T. Skills will also be required, particularly with attention to Power Point Presentation skills / Knowledge. Effective organisational skills and the ability to influence senior management will also be required.
Salary - £26-32K + Excellent Benefits (Including final salary pension scheme).
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Production Manager / Medical Devices /Pharma / Surrey /£55-60k |
| Salary/rate |
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£55000 - £60000/annum bonus and benefits |
| Location |
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Surrey |
| Job Number |
|
117190800 |
| Posted |
|
20/02/2012 (21:14) |
| Agency/Employer |
|
Cranleigh Group |
| Description
|
|
Production Manager / Medical Devices / Drug Delivery / Surrey / Hampshire / £55-£60k
An international specialist healthcare company that develops and commercialises products targeting critical care, cancer and other disorders, has an exciting opportunity for a Production Manager.
Initially you will play a key role in a new drug delivery program and will be setting up all the resources required to obtain regulatory approval for US commercialisation. This will include facility, equipment, team. materials and processes.
Ongoing you will manage all routine planning, production and team activities for the Product's manufacture and supply.
RESPONSIBILITIES:
- Establish, promote and maintain the highest standards for the environment, health and safety of all operations
- Responsible for the performance and development of all members of the production team
- Planning the overall supply plan for products and programmes and all medium to long term capacity requirements for production resources
- Stock control
- Budget management
- Managing production in accordance with a master production schedule, establishing key metrics for all operations.
- Quality and Continuous Improvement - ensuring full adherence to GMP
- Training of the production team
- Engineering, Validation and Maintenance - work with engineering and R&D to develop processes and assist with technology transfers
EDUCATION, EXPERIENCE, SKILLS AND ATTRIBUTES
- Degree in Life Science or Engineering
- Experience of setting up a new production function
- Management of production in a GMP operation in a pharmaceutical, medical device or preferably in a drug/device environment
- Mechanical and/or aerosol technology experience advantageous
- Lean Six Sigma leadership (preferably green belt qualified)
- People development and strong management skills
- Good project management skills
- Effective communication skills, written, verbal and presentation
- Able to make quick, clear decisions while under pressure
Salary £55 - £60k + bonus and excellent benefits
This position will be based at the company's facility in Surrey
Please provide a cover letter to support your application.
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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| Contact Details |
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| Job Title |
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Technology Process Development Scientist-Diagnostic-GMP-£35-45k |
| Salary/rate |
|
£35000 - £45000/annum Excellent Benefits |
| Location |
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Dartford, Kent |
| Job Number |
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120251400 |
| Posted |
|
20/02/2012 (16:51) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Technology Process Development (TPD) Senior Scientist - EIA Diagnostic Assays - GMP -Immunodiagnostics - Virology - Assay Development - Biotechnology Permanent -
Kent - £35-45K + Benefits
An international group within the in vitro diagnostics and immunodiagnostics market, providing an innovative line of products that are used in analysis laboratories at universities, hospitals and private testing facilities around the world currently require a Senior TPD Scientist.
The company is looking for a solutions orientated individual that has experience with EIA diagnostic assays using antibody technology. The successful candidate will ideally have a diagnostic/virology/blood transfusion/assay development background; and be able to demonstrate the ability to translate between assay-technologies and possibly scale/throughput to identify resource efficiencies, cost reductions and improvements.
A key responsibility of the position is the provision of technical and trouble-shooting support to both internal (CAPA investigations, technical issues, product support) and external (Customer complaints, Marketing, Regulatory) Customers. You must therefore have the ability to effectively manage customer perceptions and be confident in their communication about the technology and its technical issues.
Prompt and speedy resolution of all organisational investigations is essential; so demonstrable problems solving, interpersonal, organisational communication and time management skills would be an advantage.
To be considered for this opportunity you will hold at least a degree level qualification (Ideally a PhD or equivalent) in Immunology, Biotechnology or a related subject.
You will also possess extensive industrial experience in the biological evaluation and investigation of monoclonal antibody biology and have a thorough understanding of manufacturing processes within a GMP compliant facility. Excellent verbal communication and presentation skills will also be required along with effective team working skills.
Salary - £35-45k + Benefits dependent upon skills and experience
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Business Development Exec.-Packaging-Surrey-c£25K (OTE £38-40k) |
| Salary/rate |
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£25000 - £40000/annum Benefits |
| Location |
|
Leatherhead, Surrey |
| Job Number |
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118438499 |
| Posted |
|
17/02/2012 (18:05) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Business Development Executive - Graduate- Packaging - Paper - Print -B2B - Surrey- £20-£25k (OTE £40k)
We are currently seeking experienced B2B Business Development Executive to work for a worldwide authority in the packaging, paper and print industry supply chains.
The main duties and responsibilities of this position will include:
-Identify and pitch (manly via telephone) portfolio of information products and services to senior decision makers. This portfolio will include market research, membership information products and sponsorship opportunities.
-Account management of key customers
-Topic familiarisation through desk research
-Attend key industry events/client meetings.
-Contribution to team meetings with business managers
-Contribution to sales meetings
To be considered for this opportunity you will be a graduate in Economics, Maths, Business Studies (Or related subject), and have gained previous sales experience in a business to business environment.
This is an office based role and you will need to possess excellent verbal communication skills coupled with a strong customer focus and I.T. skills.
Salary - Basic c £25k - OTE £38 - £40k + Benefits
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Cell Culture Manager-In-Vitro Diagnostics-GMP-Kent-£45-60k |
| Salary/rate |
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£45000 - £60000/annum Benefits (Incl. Final Salary Pension |
| Location |
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Dartford, Kent |
| Job Number |
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120251301 |
| Posted |
|
17/02/2012 (17:39) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Cell Culture Manager - Monoclonal Antibodies - In Vitro Diagnostics - Six Sigma - GMP - Kent - £45K-£60K + Excellent Benefits (Incl. Final Salary pension)
This is an excellent opportunity for a Cell Culture Manager to join a global leader in in vitro diagnostics.
In this senior role you will provide scientific and technical direction relating to the production of monoclonal antibodies and recombinant antigens produced in cell cultures. This will
include product redevelopment, process redevelopment, process transfers, introduction of new technologies and process investigation/problem solving.
Major Accountabilities
* To supervise the introduction of new and redeveloped cell culture processes into manufacturing.
* To liase with R+D in the development of new products and processes.
* To liase with other sites on the transfer of new products.
* To develop cost improvements to enable the company to remain cost competitive.
* Maintain knowledge of current developments in the cell culture field and assess new technology for introduction into the company.
* To ensure the completion of all required actions as specified in the quality system, in time to support successful new product availability. New processes to be fully validated, reliable and robust and at an appropriate scale to support manufacturing requirements.
* Input into technical investigations involving cell culture processes.
* Input into scaled-up or modified cell culture processes as required by a change in business needs or as part of a cost improvement plan.
* Ensure that ERs are raised in good time and that any CAPA investigations are completed by the due date. Supervise the introduction of any changes required by the CAPA plan.
* Be familiar with and comply with all EHS rules, policies, procedures and any other instructions relevant to working in the cell culture area.
As the successful candidate you will have extensive experience of cell culture and related disciplines with a research or industrial background in cull culture, including development of cell lines and problem solving in cell culture processes and related disciplines. Additionally, you will have extensive experience of purification and related disciplines including purification processes and problem solving in purification. This is a supervisory position and it is essential that you have demonstrable leadership skills.
You must be educated to at least MSc level in a relevant scientific discipline to enable a full understanding of culture processes and their application to manufacturing. Six Sigma experience (ideally Black Belt) and Management qualification are key requirements for this opportunity.
Salary £45-60k + Excellent Benefits (Incl. Final Salary Pension)
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Purification Development Manager-Six Sigma-GMP-Kent-£45-60k |
| Salary/rate |
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£45000 - £60000/annum Benefits (Incl. Final Salary Pension |
| Location |
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Dartford, Kent |
| Job Number |
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120251289 |
| Posted |
|
17/02/2012 (17:25) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Purification Development Manager - Diagnostics-Process-Six Sigma-GMP-In-Vitro-Kent - £45K-£60K
We require a Purification Development Manager to join a global leader in in vitro diagnostics. In this senior role you will provide scientific and technical direction relating to the purification of monoclonal antibodies and recombinant antigens produced. This will include product redevelopment, process redevelopment, process transfers, introduction of new technologies and process investigation/problem solving.
As the successful candidate you will have extensive experience of purification and related disciplines with a research or industrial background in purification, including development of purification processes and problem solving in purification. This is a supervisory position and it is essential that you have demonstrable leadership skills.
Major Accountabilities
* To supervise the introduction of new and redeveloped purification processes into manufacturing.
* To liaise with R+D in the development of new products and processes.
* To liaise with other sites on the transfer of new products.
* To develop cost improvements to enable the company to remain cost competitive.
* Maintain knowledge of current developments in the purification field and assess new technology for introduction into the company.
* To ensure the completion of all required actions as specified in the quality system, in time to support successful new product availability. New processes to be fully validated, reliable and robust and at an appropriate scale to support manufacturing requirements.
* Input into technical investigations involving purification processes.
* Input into scaled-up or modified purification processes as required by a change in business needs or as part of a cost improvement plan.
* Ensure that ERs are raised in good time and that any CAPA investigations are completed by the due date. Supervise the introduction of any changes required by the CAPA plan.
* Be familiar with and comply with all EHS rules, policies, procedures and any other instructions relevant to working in the purification area
You must be educated to at least MSc level in a relevant scientific discipline to enable a full understanding of culture processes and their application to manufacturing. Six Sigma experience (ideally Black Belt) and a Management qualification are key requirements for this opportunity.
Salary - c£45-60k + Excellent Benefits Incl. Final Salary Pension Scheme
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| Job Type |
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Permanent |
| Contract Length |
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Permanent |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Microbiology Technical Advisor-Food-HACCP-Surrey-£25-28k |
| Salary/rate |
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£25000 - £28000/annum Excellent Benefits |
| Location |
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Surrey |
| Job Number |
|
120251276 |
| Posted |
|
17/02/2012 (17:07) |
| Agency/Employer |
|
Cranleigh Group |
| Description
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Senior Microbiology Technical Advisor - Food Microbiology - HACCP- Permanent - Surrey - £25-28k
An international food and research consultancy currently requires a Senior Scientific Technical Advisor with first class microbiology knowledge to provide a professional & timely scientific and technical enquiry service. You will also be required to produce and deliver publications and organise conferences in a timely and professional manner. This is an ideal opportunity for someone who is looking to take their lab based knowledge and apply it within a more commercial 'desk based' role
Main Accountabilities:
People
* To service enquiries (internal and external customers and clients) professionally utilising strong interpersonal skills.
* To have the ability to identify customer needs and provide clear advice where appropriate.
* To display excellent communication skills required for approaching, meeting and completing projects with potential and existing clients.
Planning
Excellent planning skills required for:
* Management of customer enquiries.
* Production and publication of assigned publication titles and editorial.
* Identification and organisation of technical conferences.
* Identifying opportunities for confidential project work. This will involve awareness of the market place, current and future trends in microbiology and food safety and ability to interpret available data and make recommendations.
* Successful completion and delivery of confidential and other projects. This will entail organising workload with the assistance of your Line Manager and delivering a final product that satisfies the customer.
The individual will be required to:
* Manage and respond to customer enquiries in a professional, scientifically valid and prompt way
* Identify potential areas for developing conferences and publications and be actively involved in their co-ordination and successful delivery.
* Update all microbiology publications assigned to them
* Deliver technical presentations, where required
* Assist in project work and reporting, where necessary
To be considered for this opportunity you will possess at least a degree level qualification in Microbiology (or related subject), and have a strong track record working in industry (ideally the food sector). You will also need to possess excellent verbal communication and presentation skills.
Salary - £25-28k + Benefits - Dependent upon qualifications & experience
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| Job Type |
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Permanent |
| Contract Length |
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Nonhe |
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ASAP |
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QA Specialist-Manufacturing-GMP-Biotechnology-Dartford-c£30-35k |
| Salary/rate |
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£30000 - £35000/annum |
| Location |
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Dartford, Kent |
| Job Number |
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120250852 |
| Posted |
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15/02/2012 (12:35) |
| Agency/Employer |
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Cranleigh Group |
| Description
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QA Specialist - Manufacturing - Diagnostics - Medical Devices - CAPA - GMP - 12 Months+ - Dartford - Kent - c£30-35K + Excellent Benefits
An international Biotechnology company currently require an experienced Quality Assurance (QA) Specialist to join their Quality Division at their site in Dartford, Kent. This is a pivotal role within the group and you will be tasked with supporting the manufacturing section for all aspects of the Quality System.
Major Responsibilities:
* To undertake the inspection of Biotech material to the authorised MQA ITR to the agreed manufacturing release schedule, ensuring that all documentation is complete and where any deviations noted take appropriate action.
* Ensure that all appropriate Biotech components have the correct product status and dating on MFG-PRO according to the test result status and as notified by authorized Manufacturing staff.
* Ensure that MQA actions for CAPA's, Site projects and Division are completed per plan.
* Responsible for the maintenance and development of the following systems within Biotech MQA
o Biotech MQA certificates of analysis
o Biotech MQA ITR templates and e-pas forms
*To deputize for MQA Manager when required.
* Authorising the release of Rare Reagents manufactured, raw materials and packaging for manufacturing use or evaluation within agreed lead times.
*To undertake Biotech workbook review/POI reviews on all biological reagents.
*To initiate or undertake QA authorization responsibilities for Exception Reports as defined in the governing procedures and policies.
*To perform MQA quarantine actions accurately to ensure that the correct status is on MFG and there are no incidences of noncompliance to the procedure.
*Responsible for familiarizing and complying with all health, safety and environmental rules, policies, procedures and any other instructions relevant to working within their area of the Company.
*To represent QA at Project groups and Technical meetings ensuring that QA actions for Biotech are progressed in line with the project plan.
*Provide support to the Biotechnology section for all aspects of the Quality System including CAPA Investigations, ERs and quarantine actions as required.
* Lead inspection readiness maintenance by walk throughs, spot checks and self-audits/ assessments of manufacturing areas as the MQA representative.
To be considered for this opportunity you will possess a strong QA background gained working in the Medical devices, Biotechnology, Diagnostics, or associated industry sectors to ensure products released meet the divisional requirements. Excellent administration skills will also be required along with strong technical skills. Ideally you will be educated to degree level or higher in a scientific discipline.
Salary c£30-35K
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| Job Type |
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Contract |
| Contract Length |
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12 Months |
| Start Date |
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ASAP |
| Contact Details |
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R&D Manager-Fuels-Additives-Oil-Industrial-Chemistry-Berkshire |
| Location |
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Reading, Berkshire |
| Job Number |
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120250841 |
| Posted |
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15/02/2012 (11:55) |
| Agency/Employer |
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Cranleigh Group |
| Description
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Manager Industrial R&D Development - NPD - Formulation - Additives - Oil - Fuels - Synthesis - Permanent - Berkshire - £ Competitive + Excellent Benefits (incl. final Salary Pension) & Career Development
Due to continued expansion we are currently seeking an experienced R&D Industrial Manager with expertise in the fuels, additives or oil sector(s) to drive through innovative NPD projects. You will be leading a group of R&D professionals and working closely with the company's Global Formulation Team whilst also collaborating with Sales & Marketing to support the business and strategic company goals.
Based at the organisations R&D HQ in Berkshire, this is a fantastic opportunity for a talented individual with first class technical and managerial skills coupled with excellent commercial acumen.
The overall purpose and focus of the opportunity will see you managing the Industrial development team whilst also supporting the industrial development chemists who are conducting projects to develop global industrial additive products. You will also work with the global analytical, mechanical and process development teams to ensure resources and priorities are sufficient to meet agreed technology delivery deadlines.
1. Day to day management supervision and support of Industrial development team including:
*Complete performance reviews for team members
*Lead the recruitment process to select new group members
*Coordinate on-the-job training for new and existing staff
*Ensure Team members' skills continue to meet business needs. Lead discussions on team development and ensure all relevant training is actioned.
*Handle disciplinary matters
*Ensure safety and quality procedures are adhered to.
2. Liaison with Sales & Marketing to ensure delivery of new technology programs for the Industrial area.
3. Work with global R&D Director to develop budgets and long range plans
4. Effective interaction with support areas such as Analytical and Rigs to ensure that workload is managed.
5. Interaction with global analytical and mechanical testing teams to ensure priorities and resources are adequate to meet technology delivery deadlines.
6. Attendance at relevant Industry meetings & seminars to represent the company's position.
7. Manage own technology development technical programs & customer interfaces.
The role requires:
*A Graduate or Ph.D. degree qualification in Chemistry or equivalent,
*Extensive industry experience
*Experience managing professionals.
*A good understanding of the Additive & Oil industry
*Excellent communication & facilitation skills
*The ability to work well with people, positive & a supportive attitude with ability to mentor individuals
*Good organization skills able to organize both self & others
*Logical thinker
Salary - £ Competitive + Excellent Benefits Package (Incl. final salary pension scheme)
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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ASAP |
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| Job Title |
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Senior Development Engineer-Mechanical-Manufacturing-Hants-£43K |
| Salary/rate |
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£40000 - £43000/annum |
| Location |
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Hampshire |
| Job Number |
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107748742 |
| Posted |
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13/02/2012 (16:23) |
| Agency/Employer |
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Cranleigh Group |
| Description
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Senior Development Engineer -Mechanical Engineering-High Precision Manufacturing-Hants- £40-£43K
Our client is a leading global manufacturer of contact lenses and aftercare solutions, manufacturing the widest range of contact lens care products in today's market.
Working closely with the Technical Director, as the Senior Development Engineer, you will be responsible for developing new products and working to improve existing products.
You will be involved in the whole process, from initial prototype stage through to full-scale production. In addition to your excellent project management skills, you must have strong communication skills in order to liaise effectively on all levels.
To be considered for this position you must have:
- Experience gained with a high procession manufacturing environment
-Project management experience, including attending steering committee meetings
-A degree in physics, mechanical engineering or similar discipline
-Excellent IT skills including working knowledge of AutoCAD
Although not essential, any experience in the contact lens industry would be a distinct advantage.
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Permanent |
| Contract Length |
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N/A |
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ASAP |
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| Job Title |
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Material Engineering Technician / Medical Devices- Surrey -£19k |
| Salary/rate |
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£17000 - £19000/annum bonus and benefits |
| Location |
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Surrey |
| Job Number |
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120250458 |
| Posted |
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10/02/2012 (22:08) |
| Agency/Employer |
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Cranleigh Group |
| Description
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Engineering Technician / Materials Science / Medical Devices / Surrey / £17-19k + bonus & benefits
This is an excellent opportunity for a Materials Science / engineering graduate to join an expanding and successful Surrey based medical devices company. As Engineering technician you will be providing technical support to varied and diverse projects being carried out and supported by the Research and Development Team. This is a technical, lab based, hands on role which will involve manufacturing and testing of developing products, in addition to collating and analysing data on the characteristics of these products.
Principal Responsibilities include:
- Providing technical support for the development, manufacture and characterisation of development products to ISO and GMP requirements
- Organising and co-ordinating the external processing and testing of products and samples
- Testing and characterising developing products by a variety of standard test methods
- Providing technical support by testing and characterising products for regulatory and marketing support
- Developing new test methods and aid in the implementation of new test equipment
- Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards
- Other reasonable tasks as required by the Line Manager
Education, Experience, Skills and Attributes
- A minimum of BSc (ideally in Materials Science or engineering) is required, however suitable engineering or hands on experience would be considered as an alternative to a formal qualification
- Laboratory / workshop experience working with chemicals in a COSHH and HASAW environment would be beneficial
- Competent with MS Office
- Experience working in a cleanroom environment is an advantage
- Experience with manufacturing medical devices to ISO13485 quality standards and working to controlled procedures or working within a highly regulated industry
- Ability to work in a team but also independently when required
- Good organisation and self discipline
- Good written and verbal communication skills
Salary in line with experience - £17 - £19k+ bonus and excellent benefits
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Permanent |
| Contract Length |
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N/A |
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| Job Title |
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Research Scientist / Strain Development /Biofuels / Surrey £30k |
| Salary/rate |
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£26000 - £30000/annum bonus and benefits |
| Location |
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Surrey |
| Job Number |
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120250456 |
| Posted |
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10/02/2012 (18:27) |
| Agency/Employer |
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Cranleigh Group |
| Description
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Research Scientist / Strain Development Project Leader / Biofuels / Molecular Biology / Surrey / up to £30k
We have an excellent opportunity for a talented scientist to join the Strain Engineering team of a leading Surrey based biofuels company. This role is a research position in which you will manage all Strain Development projects by effectively communicating objectives, result summaries and challenges within the group and to the research management team.
You will be expected to devise, develop and implement new screens to generate bacterial strains possessing improved or alternative properties and develop new bacterial strains using routine mutagenesis and protoplast fusion techniques. An important part of this role will be leading and supervising two research assistants and thus the ability to manage people positively is required
To be considered you will possess a relevant PhD together with practical experience in microbiology / molecular biology. The company is particularly interested in candidates who have experience in mutation, strain selection and/or automated high throughput screening.
This is a 12 month fixed term contract to cover maternity leave with the possibility to become permanent after this period.
Salary up to £30k plus generous performance related bonus and private healthcare.
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Contract |
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N/A |
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QC Analyst-HPLC-GC-Pharmaceutical-12 Months-Hertfordshire- £25k |
| Salary/rate |
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£24000 - £25000/annum |
| Location |
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Watford, Hertfordshire |
| Job Number |
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120250137 |
| Posted |
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09/02/2012 (11:47) |
| Agency/Employer |
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Cranleigh Group |
| Description
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QC Analyst-HPLC-GC-Pharmaceutical-LIMS-12 Months-Hertfordshire-c£25
Our client is a manufacturer of a wide range of toiletry products, pharmaceuticals and medical devices for both brand owners and retailers. They have an immediate opportunity for a skilled and experienced pharmaceutical QC Laboratory Analyst to join initially on a temporary 12 month contract.
As the successful candidate you should be educated to degree level or equivalent in Analytical Chemistry and have significant industrial experience of HPLC, GC and Wet Chemical techniques together with experience of testing raw materials and finished products (creams and liquids) and an understanding of LIMS. Previous experience in the pharmaceutical industry is therefore essential.
Additionally, you must have proven leadership skills together with the ability to mentor and train effectively together with strong communication skills as you will need to interact on a daily basis across several departments.
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| Job Type |
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Contract |
| Contract Length |
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12 months |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Senior Design Engineer-Medical Devices-Surrey-c£40-£45k + Bonus |
| Salary/rate |
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£40000 - £45000/annum Excellent Benefits |
| Location |
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Guildford, Surrey |
| Job Number |
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107746957 |
| Posted |
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09/02/2012 (10:06) |
| Agency/Employer |
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Cranleigh Group |
| Description
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Senior Design Engineer - Medical Devices - Technology Transfer - Surrey - c £40-£45k + Bonus + Excellent Benefits
An International Healthcare Company is currently seeking an experienced Design Engineer to lead the product design program for a new product line to fulfil the requirements of its product life cycle management.
Principal Responsibilities
1.Responsible for initiation and implementation of all product design changes for the product through its product life cycle.
2.Lead and recruit, if applicable, the product design team to support the product design program.
3.Work closely with the management team regarding product life cycle challenges and propose design solutions.
4.As applicable, liaise with design firms and component vendors to finalise fit-for-purpose product designs.
5.Maintain and adhere to good design practices maintaining the design history file.
6.Provide regular communications with key stakeholders.
7.Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with company values.
Education and Experience
1.MSc or PhD in mechanical engineering or equivalent
2.Experience within the Medical Device industry
3.Experience with supporting FDA and EU product submissions
4.Demonstrated experience in leading and working in teams
5.Demonstrated experience with developing design history files, risk management files and usability programs
6.Demonstrated experience in leading successful design reviews
7.Experience with combination products a plus
8.Demonstrated experience with technology transfer and manufacturing process development
9.Proven track record for delivering projects on time and in budget
Alongside the above qualifications and experience you will also need to demonstrate Strong analytical skills, the ability to handle multiple projects simultaneously and the ability to work with multinational teams
Salary - c £40-£45k + Bonus + Excellent Benefits
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Permanent |
| Contract Length |
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N/A |
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ASAP |
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