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| Job Title |
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Project Development Manager - Medical Device |
| Location |
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North Yorkshire |
| Job Number |
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120240687 |
| Posted |
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20/02/2012 (13:24) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
Description
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We are looking for a Senior Development Manager for a successful and growing medical device company in the North Yorkshire area.
You will be part of the senior management team reporting directly to the managing director. As Development Manager you will be responsible for organising and managing all development projects within agreed budgets and timelines.
Responsibilities of the role are outlined below but are not limited to these;
You will be responsible for planning, conducting and supervising all new and existing product development projects, both short and long term. You will develop and execute a programme to ensure all company commercial objectives are met.
You will manage a group of project leaders, ensuring project milestones are met by identifying project needs and assigning resources where needed. You will be responsible for motivating and developing your team through personal development plans and being on hand to offer technical advice and hands on support.
You will work closely with Business Development and manufacturing to identify, engineer and manufacture new products that fit identified markets and customer needs. You will evaluate (with Business Development) market reactions to existing products to ensure the timely adjustment of development strategy and new project opportunities.
You will ensure that the development department interfaces with clinicians and customers to gather new product information.
Working closely with Regulatory Affairs, Manufacturing & Quality Assurance/Quality Control you will ensure that the development of new products meets and/or exceeds company, EU and US quality standards.
The successful candidate will have a BSc or equivalent in a scientific discipline, preferably life science. You will have proven experience of working within teh medical device industry in a product development environment, managing multiple projects over varied timelines and budgets. You will have experience of managing a team, setting milestones and working with departments across the business.
The company focuses on biological medical device and is keen to find someone with a background in this sector, who is happy to be hands on whilst managing the overall project portfolio.
The individual will be extremely organised, be able to work under pressure and have experience of dealing with changing timelines and priorities.
For further information please contact Laura on 0845 680 5812 or apply online.
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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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Laboratory Manager |
| Salary/rate |
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£24000 - £28000/annum |
| Location |
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West Yorkshire |
| Job Number |
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120242542 |
| Posted |
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20/02/2012 (13:24) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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We have a new position available for a Laboratory Manager in a Chemical manufacturer in the West Yorkshire area. The role is a hands-on and laboratory-based involving management of staff and their workload and responsibility for quality.
Key responsibilities include:
Leadership of a small team of laboratory staff, task progression and work prioritisation.
Reports - quality, accuracy and authorization
Competitor product analysis
Product development
Raw materials - technical knowledge, evaluation and application
Instrumental method development
5S implementation in Laboratory and Laboratory Stores
Purchasing of laboratory equipment and reagents
Upkeep of ISO9000, ISO14001, MSDS, Labeling, COSHH, Risk Assessment systems
Customer quality requirements, raw material ordering requirements and product issues
Compliance with chemical legislation
Representative at Trade Association and related seminars
Rework of redundant stock, mis-blended batches, customer returns
Responsible for new product plant supervision
Formulation Cards, Packaging & Labelling specifications for production
The successful candidate will have a minimum of BSc or equivalent in Chemistry, Textile technology or related subject and have proven experience in laboratory based roles within the chemical industry. Previous lab management experience would be preferred by not essential. Ideal candidates will have legislative knowledge, including COSHH, CHiP, CLP, REACh, BPD, COMAH, ADR.
We are looking for an individual who is driven and feels comfortable in a fast paced laboratory environment. Someone who can motivate and develop their team and help to drive the business forward.
For further information on this role please contact Laura on 0845 780 5812 or apply online.
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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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Development Analyst - Pharmaceutical |
| Salary/rate |
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£20000 - £24000/annum |
| Location |
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Middlesex, South East |
| Job Number |
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120196979 |
| Posted |
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20/02/2012 (13:24) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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An excellent opportunity has arisen for a Pharmaceutical Development analyst in a growing organisation in the Middlesex area.
The role will involve carrying out analytical method development and validation of analytical techniques for numerous pharmaceutical products. The Chemist will be involved in various projects working with solid, liquid, semisolid, injectable and aerosol dosage formulations.
The successful candidate will have minimum of a BSc or equivalent in Chemistry or analytical chemistry. Previous experience of method development and validation of HPLC, GC, dissolution techniques is essential for this role. You should also have worked within the pharmaceutical/healthcare industries to qualify for this role.
The contract available is for 1-2 years dependant on skill set and experience. There may be more long term opportunities available for candidates who prove themselves in the role.
For further information please contact Laura on 0845 680 5812 or apply online.
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| Job Type |
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Contract |
| Contract Length |
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1-2 years |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Regulatory Affairs Manager - Medical Device |
| Location |
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North Yorkshire |
| Job Number |
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120246777 |
| Posted |
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08/02/2012 (17:14) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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We have a new opportunity for a Regulatory Affairs Manager within a growing medical device company situated in North Yorkshire.
The role reports directly into the Managing Director and you will manage and organise all company regulatory activity with the support of one direct report.
You will be responsible for;
X Responsible for all internal, national and international regulatory activities and objectives.
X Identify, design and implement appropriate new regulatory strategies for products. Maintain a clear view of regulatory developments to achieve this.
X Organise regulatory resources to meet requirements of the business and the regulators.
X Achieve all reasonable regulatory approvals. Work with team members to help facilitate attainment of project milestones to accomplish this goal. Prepare documentation and reports for international regulatory submissions/registrations.
X Coordinate project activities relating to achievement of regulatory approvals, such as CE Marks, PMA's, 510k's and IDE's etc
X Participate as the regulatory representative in new product development projects. Assess & review design documents, protocols and reports that will be used for regulatory submission purposes. Provide direction on regulatory paths and regulatory requirements to ensure generated documentation is appropriate for its purpose.
X Professionally represent regulatory affairs matters to internal and external customers, including the regulators. Regulatory representative of the company‘¦s management team.
X Provide a regulatory information service to the company, updating the business on new regulatory developments to encourage proactive approaches to meet the changing regulatory environment.
X Provide an independent regulatory assessment of company, commercial and project documentation as required.
X Responsible for company vigilance, recall, labelling & regulatory dossier quality systems. Ensure compliant operation to relevant regulations, directives and standards.
X Responsible for performing regulatory assessments of promotional material and change controls, including design changes relating to existing products
You will also be responsible for supporting the QA department and commercial department through input into the QMS and customer feedback and promotional material.
You will work closely with all other departments within the business to ensure work is performed in a compliant manner and products are launched on time.
You will carry out regulatory audits as and when required.
The successful candidate will have a proven career in the healthcare industry with previous experience in a senior/management regulatory role within the medical device industry. It is essential that you have worked with both EU and US regulations and have knowledge of the Medical Device Directive 93/42/EEC, ISO 13485, FDA QSR 820, 510(k) & PMA regulations. You will show a successful track record in filing, securing and supporting regulatory submissions in both the EU & US.
A lead auditor with the ability and willingness to travel overseas at relatively short notice would be an advantage.
Fro further information please contact Laura on 0845 680 5812 or apply online
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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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Laboratory Manager - Histology |
| Salary/rate |
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£30000 - £40000/annum plus benefits |
| Location |
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West Yorkshire |
| Job Number |
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120245146 |
| Posted |
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08/02/2012 (17:13) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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We have a new opportunity for a Laboratory Manager to run the histology department within a contract testing company in the West Yorkshire area.
You will coordinate the workload and oversee all histology work that comes into the laboratory. You will manage a team of laboratory scientists and technicians, providing support and technical expertise where needed.
The laboratory covers all aspects of tissue processing work, including the cutting of wet tissue, section cutting and staining (including special stains), preparation of fluid samples for cytology and some Immunohistochemistry work.
You will manage and monitor Quality assurance including preparation and development and review of SOPs. Maintain ISO17025 by ensuring documentation is up to date and training is provided for all staff.
You will review productivity levels and resolve operational/process problems by applying Lean Six Sigma thinking to all aspects of the laboratory.
The successful candidate will have a minimum of BSc (preferably a Masters) in Laboratory sciences/biomedical science or a related subject, with proven experience within all aspects of histology/cytology work.
Previous managerial/supervisory experience is essential, as the laboratory is fast paced and needs an organised and efficient manager. A good understanding of ISO17025 requirements and the importance of Quality Assurance within a laboratory environment is necessary.
If you feel you have the required skill set for this role please contact Laura on 0845 680 5812 or apply online
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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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Haematologist |
| Salary/rate |
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£15000 - £18000/annum Up to £18K |
| Location |
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Leeds, York, Wetherby, Selby, Wakefield, West Yorkshire |
| Job Number |
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120237074 |
| Posted |
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08/02/2012 (17:13) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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A new position has opened for a haematologist (biomedical scientist) within a contract diagnostic company in the West Yorkshire area.
The role is based with the haematology team and you will be carrying out analysis of samples. You will be using ADVIA and sysmex analyses for the processing of full blood counts, processing of samples for coagulation studies and reading blood film morphology to aid in the diagnosis of illness. The lab also runs a range of serology, including immuno-fluorescence and ELISA assays, so experience in these areas would be highly desirable.
The successful candidate will have a minimum of BSc or equivalent in biomedical science or a biological based subject with proven experience of working as a haematologist in a commercial or hospital laboratory. It is not essential that you are a qualified BMS.
You will be comfortable with working in a fast pace laboratory environment and have the ability to work both individually and in a team.
You will be working on a weekly rota between Mon - Fri and Tue Sat.
For further information please contact Laura on 0845 680 5812 or apply online.
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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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Technical Support Manager - Contract |
| Location |
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Northampton, Northamptonshire |
| Job Number |
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120245912 |
| Posted |
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08/02/2012 (17:13) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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We have a contract position for a technical support manager to cover a 6-12 month maternity cover for a contract testing company in Northamptonshire.
The company offers technical services to leather and product manufacturers, high street retailers and leading global brands. You will report into the Technical director and manager all technical support responsibilities for the business, liaising and interacting with the testing, sales, finance and consulting teams in order to offer a high level of customer support.
Your main responsibilities will include;
- Supporting in the positioning of BLC as the market leader for provision of technical services
- Providing customer support (directly and via sales team support) with technical issues relating to testing, information and specifications.
- Providing customer support (directly and via sales team support) in restricted substances and legislative issues on leather, textiles, plastics and other materials related to leather related products (ie footwear, handbags, watches).
- Maintaining database for restricted substances, legislation, eco-labels and brands
- Managing technical elements of selected accounts
- Managing UKAS accreditation (for 2011 onwards) and support with UKAS accreditation for 2010.
- Monitoring and proactively disseminate appropriate RSL and standards information to members, customers when appropriate and staff.
- Contributing towards industry chemical standards development; participating in European/International committees where appropriate.
- Supporting with the technical development of new business areas eg toy testing, CE marking etc
- Supporting with testing management and booking in as required
The successful candidate will ideally have a minimum of BSc or equivalent in chemical or biological sciences, with experience in a similar position in industry.
You will have a good understanding the testing of leather and product related materials (ie textiles, plastics and metals) and the relevant scientific disciplines.
You will have the ability to develop a good understanding of restricted substances within relevant legislation, Eco-labels and Brands for consumer products, along with knowledge of analytical techniques for measuring these restricted chemicals.
You will possess good knowledge of laboratory accreditation systems (ie UKAS) and have an understanding of current standards and the development processes.
This role can be very involved so we are looking for an individual with the ability to multi-task, someone who is organised and has the discipline to work within tight deadlines. Strong communication skills, both verbal and written, are essential for this role.
You will have the ability to problem solve and deal with difficult and challenging situations in an effective and direct manner.
If you are interested in this role please contact Laura on 0845 680 5812 for further information or apply online.
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| Job Type |
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Contract |
| Contract Length |
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6-12 months |
| Start Date |
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| Contact Details |
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| Job Title |
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Synthetic Polymer Chemist |
| Salary/rate |
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£40000 - £50000/annum dependant on experience |
| Location |
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South Yorkshire |
| Job Number |
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120249013 |
| Posted |
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31/01/2012 (17:14) |
| Agency/Employer |
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Agenda 1 Scientific Training & Recruitment |
| Description
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We have a position available for an experienced synthetic polymer chemist for an Energy systems company in the Sheffield region.
You will be involved in leading development work on the companys core ion exchange materials. The role will encompass both optimisation and scale up work appropriate to the range of applications currently being pursued in both electrolyser and fuel cell systems.
The successful candidate will have a PhD in a relevant subject with industry experience in polymer synthesis and characterisation. Previous experience of successful scale up of laboratory processes to engineering practice is essential to this role.
For further information about this role please contact Laura on 0845 680 5812 or apply online.
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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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