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| Job Title |
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AD Regulatory Policy and Intelligence |
| Location |
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Buckinghamshire |
| Job Number |
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120251761 |
| Posted |
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22/02/2012 (16:20) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
Description
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Associate Director, Global Regulatory Policy and Intelligence
Job purpose:
You will be responsible for identifying regulatory and legislative trends and changes that have the potential to impact the development and marketing of the Company's pharmaceutical products. You will also be responsible for providing high quality strategic input aimed at influencing the future healthcare environment. You will also be required to partner with global or regional subject matter experts and groups including Local Operating Companies to engage in direct regulatory advocacy and influencing activities relating to regulatory healthcare policies.
Main responsibilities:
Influencing the external regulatory environment:
In partnership with local operating companies, support the Company's interactions with Health Authorities on advocacy issues, fostering relationships with key decision makes in policy and legislative areas .
Lead and develop effective approaches to global or regional policy activities, including generating of positions, influencing plans, tracking and internal communication.
Participate in identifying, defining and implementing influencing strategies.
Develop effective approaches toandparticipate in Trade Associate initiatives, Health Authority meetings and consultations.
Coordinate input in to commenting on regulatory legislative texts to help shape and influence key regulatory healthcare policies.
Provide feedback to relevant personnel on current regulatory guidelines and procedures as well as emerging regulatory or legislative issues that impact the business or products.
Leveraging knowledge of the current and emerging global or regional regulatory landscape:
Support internal functions / groups through consultation and training on specific regulatory intelligence issues.
Collect, organise and manage critical regulatory intelligence information to enable easy distribution or access across all businesses in a way that best serves an advantage. This includes the support of increased utilisation if regulatory intelligence and policy across all businesses in the development of effective strategies and decision making.
Collaborate and partner withGRPI Intelligence and Knowledge Management to ensure effective and timely dissemination of Regulatory Information, Intelligence and Knowledge.
Drive the provision of regional expertise to impact the assessment of regulatory development in the external environment.
Person specification:
A degree in law, pharmacy, medicine or a life science related discipline.
Experience of working with regulatory authorities an their role in product approval and licensing.
Experience in regulatory policy activities gained through national health authority, industry or trade associations.
Excellent working knowledge of the global or regional regulatory framework and how that applies to pharmaceutical and healthcare product development.
Highly developed network amongst global or regional regulators.
Knowledge of regulatory texts, legal texts and extensive experience of regulatory affairs.
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23759 in all correspondence.
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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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Scientist - Glass, Berkshire |
| Location |
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Berkshire |
| Job Number |
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120251703 |
| Posted |
|
22/02/2012 (13:17) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Chemist - Glass, Berkshire. Our client is an industry leading Speciality Chemical Manufacturer Organisation, who are currently looking for an Chemist - Glass, to join their Catalysts and Materials Team based in Berkshire.
This role is a year contract.
Your role will be to prepare new frit compositions for key company product areas involving decorative, functional and conductive applications.
To be considered for this role you will hold a PhD in material sciences or a related discipline (or equivalent). Previous experience in preparing glass compositions and measuring key physical and chemical properties is essential. A good knowledge in constructing glass compositions from first principles is ideal however not essential.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23763 in all correspondence.
Keywords: Glass, Ceramics, Material Science, Chemical, Berkshire, Chemical Jobs,
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| Job Type |
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Contract |
| Contract Length |
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6 months + |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Mechanical Design Engineer |
| Location |
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Cambridgeshire |
| Job Number |
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107752679 |
| Posted |
|
22/02/2012 (11:59) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
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Mechanical Design Engineer - Cambs. Our client is Global Pharmaceutical Company currently searching for a Mechanical Design Engineer for a 6 month contract based in Cambridgeshire.
Our client is looking for candidates that are proficient in ProEngineer modelling, assemblies and detail drawings.
Previous experience of designing precision parts for machining and turning is essential. Experience of EDM machining and design constraints would be advantageous. Previous experience of the Pharmaceutical industry and GMP would be also be advantageous.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23758 in all correspondence.
Keywords: Pharmaceutical Jobs, Cambridgeshire, Mechanical Design Engineer, ProEngineer, GMP, Pharmaceutical, Engineering Jobs
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| Job Type |
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Contract |
| Contract Length |
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0-6 Months |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Scientist - Medical Device, Wiltshire |
| Salary/rate |
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£18000 - £30000/annum |
| Location |
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Wiltshire |
| Job Number |
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120251667 |
| Posted |
|
22/02/2012 (11:31) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
|
|
Scientist - Medical Device, Wiltshire. Our client is a rapidly expanding Diagnostic Technology Organisation who are currently looking for a number of Scientists to join their assay development team based at their site in Wiltshire.
This is a 6 month role with a strong possibility of extension.
Your responsibilities will include contributing to assay development, formulating reagents, testing of assays amongst other general laboratory duties.
To be considered for this role you will hold a PhD in Biochemistry, Molecular Biology or a related discipline (or equivalent). Previous laboratory experience is ideal. Previous experience of PCR, ELISA or other assay techniques is essential. Previous experience of writing scientific publications is also essential.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23638 in all correspondence.
Keywords: Microbiology, Molecular Biology, Biochemistry, Assay, Assay Development, Scientist, Laboratory Technician, PCR, ELISA, Wiltshire
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| Job Type |
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Contract |
| Contract Length |
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0 - 6 months |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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QA Specialist - Temp - Pharma |
| Salary/rate |
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£13 - £14/hour |
| Location |
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Berkshire |
| Job Number |
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120251650 |
| Posted |
|
22/02/2012 (10:26) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
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QA Officer - Pharma, Berkshire. My client is looking for someone to join their small team in driving improvements in GMP and quality system compliance across the site by providing guidance, support and training.
You will provide metrics, manage and develop Site Quality Systems such as Deviation Process, CAPA Process, Internal Audit Program, QIR process, Documentation control process and Change control process. You will also be responsible for the management of legacy validation documentation post-transfer and participate in projects and other activities as determined by the QA Manager. You must ensure that GMP, Quality, Health & Safety are considered in all aspects of role and manage the key Quality Processes such as Change Control, byutilising project-planning expertise and administrative skills to provide visibility of activity and documentation to enhance compliance and ensure department supports site meets any required timelines.
Auditor/auditee experience is preferred. You will possess strong data management skills and knowledge and understanding of statistics as well as excellent knowledge and application of Microsoft Office (in particular Excel). You will be educated to degree level (or equivalent) in Chemistry (ideally) or a scientific discipline. You will need to have great attention to details and be flexible.
This role may require you to take on some laboratory work, so previous lab experience would be advantageous.
The role is initially for 3 months however there is a strong chance of extension.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application forthis role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23762 in all correspondence.
Key words: QA, Quality Assurance, Pharmaceutical jobs
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| Job Type |
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Contract |
| Contract Length |
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0 - 6 months |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Medical Director Rheumatology |
| Location |
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Switzerland, Non UK |
| Job Number |
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120251647 |
| Posted |
|
22/02/2012 (10:24) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Medical Director - Rheumatology - Switzerland
This company is the division for innovative small molecules and biopharmaceuticals of the company. Its Headquarters in Switzerland, consist mostly of Research, Clinical, Marketing, Support Functions and the Divisional Management.
Description
PURPOSE OF THE ROLE
Act as Leader of clinical development strategies for rheumatology products with particular emphasis on osteoarthritis.
Medical Director to develop and execute Clinical Development strategy.
Provide scientific expertise/input to Business Development activities, to launch/post launch activities and Marketing strategies, to Medical Communications, Exploratory Medicine, Preclinical Pharmacology, and Global Drug Safety related to this therapeutic area.
KEY TASKS & RESPONSIBILITIES
Functional Tasks
Act as medical director of clinical development strategies with regard to current and future rheumatology development;
Develop (or support development) and propose the Clinical Development Plan for assigned product(s);
Provide medical/scientific input and drive the creation of relevant clinical documents or parts thereof to ensure high quality of e.g., study concept sheets, study protocols and reports, Investigator Brochures, submission/registration documents, publications, etc;
Review and sign off all clinical documents related to the clinical studies (e.g. study protocols and study reports) within area of responsibility;
Oversee allaspects related to the scientific and medical risks in collaboration with the safety representative;
Supervise the review, analysis and interpretation of study data;
Support communication of study results as assigned;
Collaborate with Clinical Trial Management members in the selection of principal investigators and recruitment of clinical study sites.
MAIN INTERFACES (in alphabetical order)
INTERNAL: Biostatistics, Business Development, Business Unit/Marketing, Chief Medical Officer, Clinical Trial Management & Monitoring, Data Management, Drug Safety, Exploratory Medicine, Legal, Medical Information, Medical Writing, Project Management, Regulatory Affairs, R&D Quality Assurance
EXTERNAL: Health Authorities, Opinion/Thought Leaders, Clinical Investigators, Academic Institutions, Scientific and Patients' Organizations
Qualifications
CANDIDATE'S PROFILE
EDUCATION/LANGUAGES
Medical Doctor (MD) specialized in the therapeutic area with experience in direct patient care
Global recognition as expert in clinical drug development with sound knowledge in osteoarthritis or cartilage injury development
Fluency in English
PROFESSIONAL & TECHNICAL SKILLS
Solid experience in pharmaceutical product development within the pharmaceutical and/or biotech industry at an international level
Strong immunology or osteoarthritis background preferred
Extensive experiences in interaction with Health Authorities in US, Europe and possibly Japan and/or China
Experience in NDA / MAA filing would be an asset
Ability to work and manage people in a matrix environment
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23615 in all correspondence.
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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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EIA Consultant - Renewables Project Manager, Yorks |
| Salary/rate |
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£28000 - £32000/annum |
| Location |
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West Yorkshire |
| Job Number |
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120251633 |
| Posted |
|
22/02/2012 (09:47) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
|
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EIA Consultant - Renewables Project Manager, Yorks. Our client, an environmental consultancy firm, is looking to appoint an Environmental Impact Assessment Consultant to act in the capacity of a Renewables Project Manager, to be based at their site in Yorkshire.
The main roles and responsibilities of this EIA Consultant/ Renewables Project Manager will be to manage the planning and environmental assessment process for small/ medium scale renewables projects, and to contribute to sales and developing business as required. You will coordinate and submit planning applications, primarily for single turbine wind schemes, as well as sourcing, instructing and managing relevant technical experts (both internal and external). You will be responsible for carrying out EIA screening and scoping and consulting with planning authorities, statutory and non-statutory consultees.
Other responsibilities will include:
- Prepare supporting documentation, including planning statements, design & access statements and environmental appraisals.
- Manage public consultation processes.
- Coordinate planning appeal process where necessary.
- Establish and maintain good relationships with clients, investors and landowners.
- Sell renewable EIA work through quotation/tender writing, relationship building, client visits and presentations.
- Facilitate contract specific financial processes, for example invoicing, forecasting and management of financial data.
In order to be considered for this EIA Consultant / Renewables Project Manager position you will have considerable experience in EIA and/ or town & country planning, preferably in a commercial environment. You will hold a degree or equivalent in a relevant environmental subject, for example; Environmental Science, EIA, Town & Country Planning, Environmental Engineering or equivalent. A full UK driving licence is an essential requirement for this role as you will be travelling to meet clients and customers. You will have a good generalist knowledge of potential environmental and technical constraints affecting renewable development and will have a proven track record of successfully selling EIA work and building relationships with clients. As well as good report writing and time management skills, you will hold excellent project management skills with a demonstrable track record of delivering work on time and to budget, with knowledge of UK planning and development control procedures. You will be numerate and proficient in the use of MS Word and Excel and in the use of email and the internet.
The following are desirable qualities:
- A second qualification in a relevant subject.
- Strong renewables focus with knowledge of the Feed-in Tariff and Renewables Obligations subsidy mechanisms.
- Accreditation or qualification in a recognised project management discipline (eg, PRINCE2, APM).
- Experience of completing feasibility assessments for renewables projects.
- Membership of a relevant professional organisation (e.g. IEMA, RTPI etc).
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlistedfor the next stage of the recruitment campaign. Entitlement to work in the EEAis essential. Please quote reference SH23757 in all correspondence.
Keywords: Environmental Impact Assessment Consultant, EIA Consultant, Renewables Project Manager, IEMA, RTPI, Town & Country Planning, Environmental Engineering, environmental consultant
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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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Medical Advisor - Interim pulmonary vascular disea |
| Location |
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South East England, South East |
| Job Number |
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120251631 |
| Posted |
|
22/02/2012 (09:25) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Interim Medical/Scientific Advisor - Pulmonary Vascular Disease (PVD) - 23760
Reporting to the Medical Team Leader PVD, Europe, Scientific Advisers will be responsible for ensuring that all materials delivered to countries by the PVD Teams accurately communicate product knowledge, are appropriate for use and meet general technical standards for European markets.
Working within the cross-functional PVD Unit the Scientific Advisor will support the development of product promotion and communications strategies, information collation and provision to the European markets and review of promotional material. The Scientific Advisor will provide evaluated, balanced information about Pfizer products to key stakeholders and, through cross-functional team working, ensure that key marketing strategies and activities are successfully implemented to achieve business objectives. The Scientific Advisor will also be required to develop a detailed understanding of pan- European regulations and codes relevant to the promotion of human pharmaceuticals and act as an advisory resource for the SCBU brand teams. The Scientific Advisor will also support the Disease Area Review Committee meetings.
Responsibilities
Scientific, Operational and strategic support:
* As part of the cross-functional PVDU, actively participate in all activities designed to provide excellence in information provision and observance of regulations and company standards.
* Provide scientific expertise to thePVDU, generating insights and playing a key role in strategic planning to identify information gaps and options for generating evidence.
* Support the planning and development of promotional materials and medical educational activities (eg symposia and congress activities, advisory boards etc) through data provision, evaluation and assessment of scientific content, ensuring that data are used and presented in an appropriate way whilst supporting the commercial needs of the European countries.
* Ensure the medical accuracy of materials, their compliance with product licenses and relevant codes of practice and that referencing is relevant and accurate.
* Generation of, provision and communication of information related to disease area
* Medical Education material generation for country medical teams eg slide kits, Q&As
* Operational excellence for medical activities eg IIR organisation and tracking etc
Qualifications
University degree in Science, Pharmacy or Health Sciences (or equivalent).
Solid experience in healthcare, pharmaceutical or related field.
Highly motivated and proactive Scientist with solid knowledge of medical marketing, clinical research and regulatory requirements.
Bilingualism is an advantage,fluency in English required.
Knowledge and experience of the TA is preferable.
Requirements:
Experience of promotional review and sign-off in Europe.
Project management experience
Experience of using literature databases
Experience working with cross-functional teams.
Ability to critique, evaluate and communicate scientific data
Detailed oriented and attention to quality
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23760 in all correspondence.
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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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Polymer Chemist / Material Scientist |
| Salary/rate |
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£25000 - £30000/annum |
| Location |
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Hertfordshire |
| Job Number |
|
120251496 |
| Posted |
|
21/02/2012 (13:13) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Polymer Chemist / Material Scientist. Our client is an industry leading Polymer Materials organisation, that specialises in the development & manufacturing of an array of polymers including adhesives, resins, paints, rubbers & more. They are currently looking for Polymer Chemists / Material Scientist to be based from their sites in both Hertfordshire & the South West of England.
As a Polymer Chemist / Material Scientist, you will be involved in running research & development studies for the range of materials from concept through to commercialisation; carrying out application testing, coupled with mechanical & physical testing; working closely with manufacturing teams during scale-up & pilot plant trials as well as liaising with customer teams throughout including presenting of projects & findings.
This is an outstanding opportunity to join a Polymer Materials organisation, which in return offers a competitive salary, excellent benefits and a supportive & progressive environmentto work in.
To be considered for this role, you will have a degree in Polymer / Materials (Science or Engineering) or Chemistry discipline (or equivalent) and demonstrated experience in polymer materials development. Experience working with customer teams would be advantageous, but it is not essential.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23755 in all correspondence.
Keywords: science jobs, polymer, chemist, material scientist, Hertfordshire, South West
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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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Toxicologist - Chemical, Oxfordshire |
| Salary/rate |
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£25000 - £40000/annum |
| Location |
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Oxfordshire |
| Job Number |
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120251482 |
| Posted |
|
21/02/2012 (11:53) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
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Toxicologist - Chemical, Oxfordshire. Our client is a world leading Chemical Manufacturer, who specialises in chemicals for the industrial, automotive & related markets. They are currently looking for a Toxicologist to join their Regulatory Team based from their state-of-the-art facilities in Oxfordshire.
As a Toxicologist, you will be part of a team providing toxicology & regulatory support to new & existing product development teams worldwide.
Your duties will include performing risk & hazard assessments for the organisation's product ranges to ensure they are used & manufactured appropriately including providing toxicology support to R&D teams; assessing toxicology &/or ecotoxicology studies and preparing regulatory dossiers; liaising with external test laboratories surrounding studies into regulatory notification schemes such as REACH as well as maintaining the toxicology databases on all substances within the organisation's portfolio.
This is an outstanding opportunity to join a Chemical Manufacturer at the forefront of their field. The organisation is willing to consider candidate's at various levels, offering in return a negotiable salary depending on experience and excellent benefits.
To be considered for thisrole, you will have demonstrated experience within a Toxicologist position gained within a Chemical industry. Working knowledge of REACH would be advantageous, but it is not essential.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quotereference ST23552 in all correspondence.
Keywords: science jobs, toxicologist, toxicology, chemical, regulatory, REACH, Oxfordshire
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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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Quality Assurance Auditor - Pharmaceuticals |
| Salary/rate |
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£27000 - £35000/annum |
| Location |
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Hertfordshire |
| Job Number |
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120251480 |
| Posted |
|
21/02/2012 (11:40) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
|
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Quality Assurance Auditor - Pharmaceuticals. Our client is a global pharmaceutical company who are currently searching for a Quality Auditor to be based within the GMP Quality Department based in Hertfordshire.
You will ensure compliance to cGMP of all activities related to the development of pharmaceutical products for use in Clinical Trials, including the Quality Management systems and you will carry out Quality compliance reviews/release of Investigational Medicinal Products for use in Clinical Trials. Other duties will include auditing and approving procedures and documents from manufacturing, analytical, packaging and service groups, reviewing and approving equipment and facilities qualification, training others as appropriate and assisting with external audits as required.
The ideal candidate will hold a BSc in a Life Science subject (or equivalent) and will have experience gained within relevant departments of Pharmaceutical companies, preferably Quality Assurance. You will have a good working knowledge of cGMPs. An understanding of Clinical Supplies requirements would be advantageous.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference ST23754 in all correspondence.
Keywords: QA Auditor, Quality Assurance, GMP, Pharmaceutical , Hertfordshire
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| Job Type |
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Contract |
| Contract Length |
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0-6 Months |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Field Sales Executive- Waste& Environmental, WMids |
| Location |
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West Midlands, UK |
| Job Number |
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120251479 |
| Posted |
|
21/02/2012 (11:38) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Field Sales Executive - Waste & Environmental, WMids. Our client, a market leading Hazardous Waste Company based in the west midlands, is now recruiting for a field sales executive.
The main roles and responsibilities of this Field Sales Executive will be to secure new business as well as maintaining already successful accounts. You will be responsible for arranging meetings with clients as well as sourcing new business and attending trade shows for networking opportunities to increase saleswithin your given area. The company are experiencing rapid growth and is very interested in speaking with positive, motivated and successful sales people from within the hazardous waste market.
In order to be considered for this Field Sales Executive position you will have a number of years' experience within the Waste/ Environmental sector, ideally holding a scientific qualification. You should be able to demonstrate a proven track record within your field and will be organized and punctual, as well as a confident and committed individual with a desire to succeed.
The position offers a very attractive package for the right candidate.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you have not heard back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH23753 in all correspondence.
Keywords: science recruitment, chemistry jobs, waste chemist, reception chemist, field sales executive, hazardous waste, waste transfer, waste sales
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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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Interim MA Oncology |
| Location |
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Bedfordshire |
| Job Number |
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120251471 |
| Posted |
|
21/02/2012 (10:58) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
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Interim Medical Affairs Advisor - Oncology and Infection - 23752 (6 month assignment) UK
To be the Therapy Area clinical expert delivering medical insight and governance into the Brand, in order to meet Brand and Therapy Area objectives through Medical Excellence
Ensure the patient is at the heart of the Brand in all activities
Lead the development and implementation of Clinical Advisory Boards
Develop and leverage medical insight from external and internal customers into the Medical and Therapy Area plans
Develop and maintain scientific relationships with key physicians to build customer insight and develop strategic partnerships
Act as a role model and ensure ethical/professional behaviour
Ensure that Company and UKMC activities comply with standards for medical governance and duty of care
Responsible for the medical review of adverse event reports and pharmacovigilance activities*
Support Medical Affairs Scientist in driving the delivery of local strategic claim plans
Lead on the design and development of local/Regional clinical studies in line with the Medical Brand Strategy
Support or deputise for the Medical Affairs Leader in delivering Medical and Regulatory input into the Brand Strategy
Develop and drive interactions with Global and EU Medical to maximize UK influence on Global strategy
QUALIFICATIONS, TRAINING, PROFESSIONAL MEMBERSHIPS or ACCREDITATIONS
Essential:
Medicine [GMC registered] and/or extensive relevant clinical experience with appropriate professional qualification
Technical specialist requirements may vary according to business need
*In the above role profile the activities marked with * may only be undertaken by those with relevant qualifications e.g. GMC registration.In the event that the post-holder does not possess the relevant qualifications to undertake these additional activities they will be delegated to another suitably qualified member of the team
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitmentcampaign. Entitlement to work in the EEA is essential. Please quote reference CL23752 in all correspondence.
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| Job Type |
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Contract |
| Contract Length |
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6 months + |
| Start Date |
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ASAP |
| Contact Details |
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| Job Title |
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Pharmaceutical Business Lead |
| Location |
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Cambridge, Cambridgeshire |
| Job Number |
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113582647 |
| Posted |
|
21/02/2012 (10:28) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
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Pharmaceutical Sales and Marketing Lead - Cambridge
As the name would suggest, the Pharmaceutical Business Lead is the lead of the Product Marketing Team within this well established company's NEW Pharmaceutical division.
The role will require the development, implementation and effective management of a sound product and sales and marketing strategy, to ensure a profitable P&L for the pharmaceutical clinical trials sector of business within our client and the products developed for it. This will include sales of the existing product range within this sector, the development of a strategy for the development of a pharma/healthcare customer base. This must include strategic positioning as a leading provider of real-time and retrospective, remote subject monitoring and data management services for e-clinical trials.
Not only will you be responsible for the sales and marketing aspects, you will define strategy, develop the pricing structure and identify paths to market.
This is an amazing opportunity to join an organisation that is growing and ring your expertise from the Pharmaceutical / Healthcare background to help develop an entirely new market in the UK. There are some fantastic long term prospects to grow the company and take on greater leadership responsibilities as you build your team around you.
CK IT is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference IT23738 in all correspondence.
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Permanent |
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N/A |
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ASAP |
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| Job Title |
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Laboratory Supervisor |
| Salary/rate |
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£23000 - £28000/annum |
| Location |
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South Yorkshire |
| Job Number |
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120251396 |
| Posted |
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20/02/2012 (16:39) |
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CK Group (Science, Clinical & IT) |
| Description
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A food waste rendering company based in Yorkshire is looking to recruit a Laboratory Supervisor to work at their site on a permanent basis.
The role will involve the analysis of products using Gas Chromatography (GC) and various other analyticaltechniques as well as other adhoc duties.
Essential skills:
UKAS experience is a requirement and experience in LIMS would be an advantage.
Prior experience in analysis, especially in wet chemistry and ideally GC.
Previous supervisory experience would be desirable.
The successful candidate will be degree qualified in Food Sciences or equivalent. A UK drivers license is required as travel is required to other UK sites.
If you do not hear back from us within 5 working days of yourapplication for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH23750 in all correspondence.
Keywords: science jobs, laboratory jobs, analytical chemist, GC, food, UKAS, LIMS,
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Permanent |
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N/A |
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Quality Control Assistant |
| Location |
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East Midlands, UK |
| Job Number |
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120251393 |
| Posted |
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20/02/2012 (16:35) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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My client is a leading manufacturer of pet health and behavioural products and they are currently looking to recruit an Quality Control Assistant to work on a permanent basis. This role is ideally suited for recent graduates.
This is an opportunity for a highly organised person to work as part of the Quality Control team in a fast paced, GMP-centred environment.
You will be required to perform production and packing line checks, Quality Control checks of incoming materials & components, including some laboratory analyses; you will ensure all retained samples are stored appropriately, implement all corrective actions as required, and ensure compliance with all GMP procedures.
The successful candidate would be qualified to 'A' level standards especially in chemistry may be an advantage
Experience of working in Quality Control in a manufacturing and laboratory environment would be beneficial. Knowledge of HACCP, COSHH, Quality Risk Management and Quality Assurance would alsobe advantageous.
The ideal candidate will be positive, confident, proactive and highly organised with IT skills including Microsoft Word, Excel and Outlook; have strong written and verbal communication skills, a high level of accuracy and attention to detail, the ability to follow procedures, and good time management skills.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH23737 in all correspondence.
Keywords: science jobs, laboratory jobs, analytical chemist, QC Chemist, HPLC, Lincolnshire, COSHH, HACCP, MicrosoftOffice, Quality Assusrance
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Permanent |
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N/A |
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CSV Specialist - Scotland |
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£27000 - £30000/annum |
| Location |
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Scotland |
| Job Number |
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120251387 |
| Posted |
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20/02/2012 (16:07) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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CSV Specialist - Scotland. Our client, a pharmaceutical service company located in Central Belt of Scotland require a CSV Specialist to work with them on initially a 12 month contract.
The successful person will be responsible for assuring computer system regulatory compliance following industry regulations and standards including FA, MHRA and GAMP. They will be also be required to maintain knowledge of industry developments in computer systems validation and 21 CFR Part 11.
The ideal candidate will have a science based qualification and will have experience working in a cGMP environment.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference DH23748 in all correspondence.
Keywords: science jobs, science recruitment, csv specialist, computer system validation, 21 CFR Part 11, FDA, MHRA, quality compliance, regulatory compliance.
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Contract |
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6 months + |
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Clinical Outsourcing Manager |
| Salary/rate |
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£40000 - £45000/annum |
| Location |
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South East England, South East |
| Job Number |
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120251385 |
| Posted |
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20/02/2012 (15:28) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Clinical Outsourcing Manager
Permanent
Competitive salary and benefits
Hertfordshire
An exciting opportunity has arisen at the EU Head Quarters of an international pharmaceutical company. The successful candidate will manage a range of activities around the outsourcing of clinical studies. This will span negotiation and maintenance of contracts with CROs and other third party suppliers, managing their performance and monitoring budgets, metrics and audit status.
Specific duties will include:
- Support of outsourcing needs for global clinical trails of all phases
- Leading RFP development through to vendor selection and contract execution
- Coordinating the preparation and review of contract documentation
- Leading the qualification and evaluation process for new providers
- Supporting project teams when resolving third party performance issues
Experience required
Strong contract negotiation and management experience gained within a pharmaceutical company of CRO
Proven budgetary management experience
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23736 in all correspondence.
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Permanent |
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N/A |
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ASAP |
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Process Improvement Manager - East Midlands |
| Location |
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East Midlands, UK |
| Job Number |
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120251347 |
| Posted |
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20/02/2012 (11:55) |
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CK Group (Science, Clinical & IT) |
| Description
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Process Improvement Manager - East Midlands. Our client, a major healthcare organisation, is currently seeking to recruit a Process Improvement Manager to join their team.
As Process Improvement Manager you will provide focus on the developmentof new and existing processes. By building quality in to the process design our products will be produced in the most efficient way and meet the customer and regulatory needs.
You will be responsible for leading the Process Improvement Team to provide an efficient service to optimise manufacturing and cleaning processes using a Quality By Design approach whilst ensuring the validation activities meet Regulatory and Customer requirements.
The job holder will need to provide an effective New Product Introduction service for Clinical Trial clients to ensure new products are introduced successfully and that the processes are developed and validated to ensure the required levels of product quality and regulatory compliance are met. You willalso need to deliver a comprehensive process, equipment and cleaning validation programme in accordance with cGMP and Customer requirements.
To be considered for this position you will have previous experience in the development or manufacture ofhealthcare products with a proven track record of new product introduction is critical to this role. In depth knowledge of cGMP, multiple dosage forms with an emphasis on sterile products and an awareness of Unlicensed and Licensed Legislation are key to your success in this role and previous leadership and management skills would be an advantage.
You will enjoy working cross functionally in a fast paced environment with teams of diverse people, have a can do attitude with the capability to plan and see the bigger picture, excellent Leadership and Customer Service skills and the ability to influence and build relationships at all levels across the business.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH23746 in all correspondence.
Keywords: scientific jobs, science recruitment, process, technical, chemistry jobs, process, improvement
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Permanent |
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Temp - perm |
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Medical Devices Sterile Specialist |
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£40000 - £45000/annum |
| Location |
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East Midlands, UK |
| Job Number |
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120251344 |
| Posted |
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20/02/2012 (11:43) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Our client is looking to recruit a Medical Device Sterile Products Specialist on a permanent basis. This role is a home based role but travel within the UK and internationally is required. A drivers license is required for this role.
Purpose of the job:
- Primarily providing Medical Device Sterile Products consultancy
- Additionally providing Medical Devices Regulatory and Quality Management Systems consultancy
- Devise and deliver training courses to customers
- Provide a high qualityservice to all of the clients customers
Main responsibilities:
- Provide consultation on Sterile products:
- Gamma Irradiation validation and routine requirements
- Electron beam Irradiation validation and routine requirements
- Ethylene Oxidegas validation and routine requirements
- Cleanroom Operations and Environmental Monitoring
- Product Packaging
- Out of Specification/CAPA/NCF investigations & resolutions
- Implications of Design Change
- Provide consultation on Quality Management Systems
- ISO 13485
- 21 CFR 820
- ISO 13485 CMDCAS and other Quality System standards as applicable to our customers
- Write documentation including Technical Files, Design Dossiers, manuals, forms, templates, procedures etc asrequired for regulatory compliance of Customer's products
- Write documentation including manuals, forms, templates, procedures etc as required to implement Management Systems
- Provide consultation on medical devices guidance documents (MEDDEVs, NBMEDs, TS, TIR
- Attend sales meeting with customers if required
- Support the Sales Team in pre-sales and marketing activities
- Attend training courses if required
Essential skills:
- Practical working knowledge of irradiation sterilisation methods
- Knowledge of EtO sterilization
- Knowledge of validation methods for sterilisation
- Environmental monitoring of clean rooms
- Thorough and practical working knowledge of ISO 13485
- Practical working knowledge of Medical Devices Directive93/42/EEC and 2007/47/EC
- Full UK driving licence and a car owner
The ideal candidate will be degree qualified in Life Sciences, Microbiology or equivalent.
If you do not hear back from us within 5 working days of your application for this role, itmeans that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH23557 in all correspondence.
Keywords: science jobs, Medical devices, sterile, microbiology, sterilization, ISO 13485, medical devices directive, QMS
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