 |
| Job Title |
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Pharmaceutical Analyst - Central Belt of Scotland |
| Salary/rate |
|
£18000 - £21000/annum |
| Location |
|
Central Belt, Central Scotland |
| Job Number |
|
120250017 |
| Posted |
|
08/02/2012 (13:50) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
Description
|
|
BioChemist - Central Belt of Scotland. CK Science is currently recruiting for a BioChemist to work with our client a biotechnology company located in Central Belt of Scotland on initially a 6 month contract.
Working in the Quality Control laboratory the successful candidate will be responsible for performing analysis on raw materials and final products to GMP/GLP. You will carry out a number of tests including HPLC, ELISA and SDS-PAGE. In addition, you will also perform analysis using UV, IR and wet chemistry techniques.
Ideally, you will be qualified in a life sciences subject and/or have demonstrable working experience in an analytical laboratory.
CK Science is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference DH23682 in all correspondence.
Keywords: science jobs, science recruitment, biochemist, chemist, lab chemist, laboratory chemist, analytical chemist, lab analyst, GMP, SDS PAGE, ELSA, HPLC.
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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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Chemist, Environmental - Hampshire. |
| Salary/rate |
|
£13000 - £18000/annum |
| Location |
|
Hampshire |
| Job Number |
|
120250015 |
| Posted |
|
08/02/2012 (13:41) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Chemist, Environmental - Hampshire. Our client is an Environmental company looking for a Chemist to work on a 9 month contract basis.
The responsibilities will include sample preparation and analysis of water, wastewater, sewage, sludge and associated material. Analytical duties may include analysis for metals, nutrients, pH, conductivity, hardness, BOD, COD, TOC, anions, suspended solids, absorbance/transmittance, trace organics and repair/calibration of portable gas monitors. It is essential you have experience with analytical techniques which may include HPLC, GC, LC-MS, GC-MS, ion chromatography, gravimetric, fluorescence and spectrometric analysis, titration, chemiluminescence and use of BOD robot.
Once trained, you will be working unsupervised, organising your own workload to meet deadlines and take responsibility for the day to day running of analyses and allocated tasks.
You will possess a degree (or equivalent) in a Chemistry related subject and must be able to workunsupervised within a team. The person needs to be methodical in approach and have good communication, organisation and numerical skills together with an ability to handle multiple priorities and work accurately.
This is a temporary role for 9 months.
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 ST23671 in all correspondence.
Keywords: Chemist, Chemistry, analytical, HPLC, environmental
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| Job Type |
|
Contract |
| Contract Length |
|
6 Months+ |
| Start Date |
|
April 2012 |
| Contact Details |
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| Job Title |
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Analyst - Temp - Pharma |
| Salary/rate |
|
£10.50 - £11.50/hour |
| Location |
|
Hertfordshire |
| Job Number |
|
120250014 |
| Posted |
|
08/02/2012 (13:36) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Analyst, Temporary. My client is a pharmaceutical organisation who are looking for a Laboratory Analyst to join their team for 6 months.
Working within a Quality Assurance testing labortory You will be experienced in the use of analytical techniques such as HPLC, GC, UV and IR and be competent in routine testing pharmaceutical products.
You possess a degree (or equivalent) in a Chemistry or related subject and practical experience within a pharmaceutical laboratory would be advantageous.
This role is for a period of 6 months with the possiblity of extension.
Key words: Analytical, Analyst, Laboratory jobs, pharmaceutical 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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Principal Ecologist / Manager - Oxfordshire |
| Salary/rate |
|
£38000 - £45000/annum |
| Location |
|
Oxfordshire |
| Job Number |
|
120250002 |
| Posted |
|
08/02/2012 (12:07) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Principal Ecologist / Manager - Oxfordshire. Our client is a leading Environmental Consultancy who provides Consultancy Services & Policy Advice to customers across Chemical, Utility, Food & Drink, Transport & Agriculture industries. They are currently looking for a Principal Ecologist / Manager to lead their Ecology Team based at their site in Oxfordshire.
As the Principal Ecologist / Manager, you will be responsible for leading a team providing services to customers in the Utility, Rail & Developer industries across the South of the UK.
Your duties will include, day-to-day people management of a team of Ecology Consultants; leading the development & delivery of services including preparing & implementing marketing & business development plans; ensure all projects are rolled out in line with licences & quality standards (ISO 9001 & ISO 14001) as well as building strong relationships with customer teams.
The hands on element to the role will also see you managing complex & high profile projects; undertaking high level consultancy for EPS licensing and research as well as maintaining up to date knowledge of developments in habitats, species & EIA legislation.
This is an outstanding opportunity to join a leader in the field of Environmental Consultancy, which in return offers an attractive salary & benefits package.
To be considered for this role, you will have a degree in an Ecological or Natural Science discipline (or equivalent) and some or all of the below:
- Demonstrated team leader / management & business development experience in the ecology field.
- Experience carrying out environmental impact assessments & complex development projects.
- Working knowledge of habitats, protected species and planning legislation in the UK & Europe.
- Proven knowledge of survey or disturbance licences for at least one relevant EPS.
CK Science is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you donot 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 ST23680 in all correspondence.
Keywords: science jobs, ecologist, ecology, manager, environmental, Oxfordshire
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
|
Therapy Area Advisor |
| Location |
|
Hertfordshire |
| Job Number |
|
120250000 |
| Posted |
|
08/02/2012 (12:02) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Therapy Area Advisor / Scientific Advisor / Permanent
Background:
We are recruiting for a Therapy Area Advisor to join a Pharmaceutical company based in Hertfordshire. This is not a pure Medical Information role. This role will have a strong focus on working with the brand teams, doing copy approval work. The position will focus around providing supporting data and medical writing activities. Experience in Oncology therapy area would be beneficial.
Key responsibilities:
- Support the appropriate medico-marketing teams in all areas of activity as necessary, including provision of marketing and product support e.g. Business Planning, developing promotional materials, attending meetings, inputting into NICE/SMC submissions
- Supportproduction of NICE/SMC submissions as required
- In conjunction with the Medical Managers and MLMs, provides back up product support to relevant external groups when required e.g. KOLs; specialist nurse meetings
- Provide support for product issue management e.g. assists in the production of Dear Doctor letters
- Prioritise and reviews product specific activities to ensure the value MI brings to the business is maximised
- Provide input into development of the Brand key messages and strategy, to sign off documentation as part of the copy approval process in a timely fashion; and to identify where breaches of ABPI code occur
- Support development of the brand key messages and brand strategy, and use this knowledge when giving advice and approving/producing materials
- Support copy approval by undertaking detailed, thorough and minute checking of materials - data accuracy checker including accurate references, factual assertions, typos and grammar
- Act as the originator or approver on Zinc for MLM generated materials as necessary
Informs the Manager of the Therapy Area Advisors when the Active Materials list needs updating and when expired items need withdrawing from Zinc
- Disseminate information to internal customers including the Brand teams; Healthcare Management and Medical Managers to ensure accurate up to date information is available when making business decisions
- Design and deliver relevant training on the SPC and standard clinical data for the Training Specialists and provide other relevant training needs e.g. complex clinical data for the Sales Representatives
- Develop in-depth knowledge on allocated products and maintain a current understanding on new developments in specific therapy area(s)
-Communicate information to the Medical Information Specialist and Medical Information Quality, Training and Effectiveness Manager
- Evaluate and adapts any training sessions as necessary to facilitate transfer of learning to the workplace
- Provideregular updates to the relevant Medical Information Specialist regarding for instance marketing activities; brand strategies and key messages to support the production of up to date Medical Responses/Standard letters
- Provide back up support to the Medical Information Specialist team when required for the production of medical responses
- Feed back to the Medical Information Quality, Training and Effectiveness Manager any quality; process or training issues; implements initiatives cascadeddown and takes part in quality measures/relevant training
- All staff to take personal responsibility for ensuring that they maintain high ethical standards in all that they do, and that they comply with all applicable laws, regulations, industry codes and internal policies and procedures
Benefits:
Successful candidates will enjoy the benefits of working with a global Pharmaceutical company, including a COMPETITIVE SALARY, HOLIDAYS, and CAREER PROGRESSION.
Qualifications:
- Life Science Degree or higher post graduate qualification
- Previous Medical Information/Therapy Experience
- Good written and verbal communication
- Ability to prioritise workloads and to negotiate and meet deadlines
- Customer focused
- Team player
- Flexible approach
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on thisoccasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23673 in all correspondence.
Keywords: Therapy Area Advisor, Scientific Advisor, Medical Information, Medical Information Advisor, ABPI Code of Practice, Life Science, Pharmacy, Commercial Awareness, Key Opinion Leaders, Health Care Professionals, oncology, permanent
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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 |
|
Medical Manager - Rheumatology |
| Location |
|
Hertfordshire |
| Job Number |
|
120249996 |
| Posted |
|
08/02/2012 (11:54) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Job Profile: Medical Manager (Rheumatology) 23678
Purpose: To provide excellent medical affairs support which will result in maximising the potential of the pharmaceutical business for the brand and/or indication under their responsibility whilstfulfilling all regulatory/compliance obligations.
Primary Responsibilities:
To research, collate, present and offer expert opinion on scientific, medical and regulatory information to support both internal and external customers
Support key account management (KAM) with attendance at extended KAM meetings
To identify and develop strong, sustainable relationships with external Opinion Leaders to deliver both opportunity and provision to execute the product strategy
To develop, designor advise on, and manage, UK clinical trial programmes and strategic clinical issues, maximising the marketing / selling opportunity of the product at both a local and international level
To manage the integrity and accuracy of scientific, medical and regulatory data communicated both internally and externally for both promotional and non-promotional purposes, including delivering appropriate
Desirable Knowledge and Experience:
· Medically qualified with GMC registration or post graduate qualification in Life Sciences or equivalent (eg PhD, MSc), or degree and specific experience for job
· Trained and familiar with the ABPI Code of Practice
· Relevant Pharmaceutical industry experience
· Knowledge of relevant therapy area
· Knowledge of NHS environment
· Experienced in presenting, data analysis and statistics, team work and communication
· MS Office, particularly Powerpoint
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 EEAisessential. Please quote reference CL23678 in all correspondence.
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| Job Type |
|
Permanent |
| Contract Length |
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N/A |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
|
Medical Manager (Oncology) |
| Location |
|
Hertfordshire |
| Job Number |
|
120249992 |
| Posted |
|
08/02/2012 (11:39) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Job Profile: Medical Manager (Oncology) 23649
Purpose: To provide excellent medical affairs support which will result in maximising the potential of the pharmaceutical business for the brand and/or indication under their responsibility whilst fulfilling all regulatory/compliance obligations.
Primary Responsibilities:
To research, collate, present and offer expert opinion on scientific, medical and regulatory information to support both internal and external customers
Support key account management (KAM) with attendance at extended KAM meetings
To identify and develop strong, sustainable relationships with external Opinion Leaders to deliver both opportunity and provision to execute the product strategy
To develop, design or advise on, and manage, UK clinical trial programmes and strategic clinical issues, maximising the marketing/selling opportunity of the product at both a local and international level
To manage the integrity and accuracy of scientific, medical and regulatory data communicated both internally and externally for both promotional and non-promotional purposes, including delivering appropriate
Desirable Knowledge and Experience:
· Medically qualified with GMC registration or post graduate qualification in Life Sciences or equivalent (eg PhD, MSc), or degree and specific experience for job
· Trained and familiar with the ABPI Code of Practice
· Relevant Pharmaceutical industry experience
· Knowledge of relevant therapy area
· Knowledge of NHS environment
· Experienced in presenting, data analysis and statistics, team work and communication
· MS Office, particularly Powerpoint
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 CL23649 in all correspondence.
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| Job Type |
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Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
|
Analytical Chemist |
| Salary/rate |
|
£15500 - £19000/annum |
| Location |
|
East Midlands, UK |
| Job Number |
|
120249972 |
| Posted |
|
08/02/2012 (11:03) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Analytical Chemist - East Midlands. Our client is currently seeking to recruit an Analytical Chemist to work with them at their site in the East Midlands on a permanent basis.
The role will involve the analysis of incoming materials, licensed and unlicensed finished products and stability samples using techniques including HPLC, GC, AA, TOC, FTIR, UV and wet chemistry.
The ideal candidate for the role will be educated to degree level, or equivalent, in Chemistry and have experience using analytical techniques such as HPLC, AA and GC.
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 SH23457 in all correspondence.
Keywords: Science jobs, analytical jobs, pharmaceutical jobs, chemistry, analytical chemist, analyst, HPLC
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
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Method Developer - East Midlands |
| Salary/rate |
|
£20000 - £25000/annum |
| Location |
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Nottingham, Nottinghamshire |
| Job Number |
|
120249957 |
| Posted |
|
08/02/2012 (10:09) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Method Developer - Pharmaceuticals. Our client, a large Pharmaceutical manufacturer based in the East Midlands, is seeking a Method Developer on a temporary basis. The role will involve developing new methods and analytical support for the development of new products and the maintenance of existing markets.
It is essential that you have some experience of method development in ideally both HPLC and GC methods, and also have worked in the Pharmaceutical industry as minimal training will be provided for this role. The role is a contract position so you will need to be able to start work as soon as possible (short notice period required).
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 SH23468 in all correspondence.
Keywords: Pharmaceutical, method development, analytical, chemisty, HPLC, GC, scientific recruitment, science recruitment
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| Job Type |
|
Contract |
| Contract Length |
|
0-6 Months |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
|
Snr Medical Director Multiple Sclerosis |
| Location |
|
Rockville, Non UK |
| Job Number |
|
120249956 |
| Posted |
|
08/02/2012 (10:06) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Senior Medical Director - Multiple Sclerosis - Rockville USA - 23613
Description
Purpose of the Role
· Act as trial director or Medical Responsible
· Co-lead or be member of the Clinical Development Team (CDT)
· May act as a Global Product Team (GPT) clinical representative
· Provide medical-scientific input into the biomarker strategy in alignment with respective interface functions
· Provide medical and scientific expertise/input to Business Development activities, to launch/post launch activities and Global Business Unit (GBU) strategies, to Medical Communications, Research, Preclinical Pharmacology, Biomarker development strategies, Clinical Operations, Regulatory Affairs, and Global Drug Safety
Key Tasks & Responsibilities
Act as trial director:
· Oversee all medical-scientific aspects of the clinical trial(s) within area of responsibility and provide guidance to the respective trial team
· Provide medical/scientific input and drive/contribute to the creationof 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 ensure sign off of all clinical documents related to the clinical studies (e.g. study protocols and study reports) within area of responsibility
· Oversee all aspects related to the scientific and medical risks in collaboration with the respective safety representative
· Collaborate with Clinical Trial Management in Vendor surveillance/management activities
· Lead the review, analysis and interpretation of study data
· Support communication of study results as assigned
Co-lead or be member of the Clinical Development Team:
· Propose clinical development strategies for assigned product(s) in order to establish its safety and efficacy and support timely registration worldwide
· Develop and prepare clinical development plans, study concept sheets, and study protocols in collaboration with clinical and project team members
· Collaborate with Clinical Trial Management members in the selection of principal investigators and clinical study sites
Act as a Global Product Team representative:
· Participatein cross-functional development project team activities to provide medical/scientific input into e.g. business plan, project strategy, in-/out-licensing activities and Due Diligence as assigned
· Liaise with (principal) investigators, health authorities, IEC/IRB, consultants, opinion/thought leaders and academic institutions in area of responsibility
Main Interfaces
INTERNALLY: 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
EXTERNALLY: Health Authorities, Opinion/Thought Leaders, Clinical Investigators, Academic Institutions, Scientific and Patients' Organizations
Qualifications
Education & Languages
· Medical Doctor (MD) specialized in Neurology with at least 5 years experience in clinical R&D (phase I to IV)
· Experience in MultipleSclerosis
· Fluency in English
Professional & Technical Skills
· Experiences in pharmaceutical product development at an international level with experiences in interaction with Health Authorities in Europe, US and possibly Japan and/or China
· Working knowledge in ICH-GCP and other applicable regulatory guidelines/practices
· Ability to work in a matrix environment
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
Ifyou 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 CL23613 in all correspondence.
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| Job Type |
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Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
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| Job Title |
|
Medical Affairs Pharmacist |
| Location |
|
Hertfordshire |
| Job Number |
|
120249949 |
| Posted |
|
08/02/2012 (09:41) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Medical Affairs Pharmacist
KEY RESULT AREAS & MAIN DUTIES
This position is responsible for the overall supervision of the company Aesthetics Pharmacy; ensuring that company meets it's, ethical and legal obligations. This role also includes final signatory for the ABPI code compliance systems and the provision of high quality medical information services for both internal and external stakeholders.
This will include the following:
ABPI Code of Practice
- Acting as final signatory for company promotional material, as required by legislation and the ABPI Code of Practice.
- Advise on compliance related issues;
o Develop and manage UK procedures relating to Promotional Practices.
o Oversee and manage the promotional system.
o Support activities around inspections against promotional standards.
o Audit against relevant policies and procedures and identify gaps to improve business processes.
o Oversee and document training
- Assist the Head of Medical Affairs in the development of responses to ABPI Code complaints
Pharmacy
· Act as Superintendent Pharmacist for the company Aesthetics Pharmacy
· Responsible for the compliance of the pharmacy with required legislation and guidelines. Responsible for staying up to date with relevant pharmacy legislation and updating senior management as required.
· Carry out the tasks of a Responsible Pharmacist as required.
· Responsible for ensuring that all pharmacy SOPs and processes are up to date and adhered to. Driving the pharmacy to hit its profitability targets
Medical Information
· Preparation of high-quality, accurate and timely medical and technical responses to internal/external customer enquiries relating to company products, through the retrieval and evaluation of quality information using internal and external sources.
· Ensuring all Medical Information, FAQs, literature and information sources for the products are updated on a regular basis with current best knowledge.
· Provision of product training to internal and external staff according to company SOPs and guidelines.
· Mentoring junior medical information staff on medical information processes as and when required.
· Ensuring that all Adverse Events reported by customers are forwarded to the Drug Safety Department in an expedited manner and in accordance with company SOPs and guidelines.
· Act as a Departmental Ambassador. Establish close working relationships with other company departmentsboth local and global e.g. Sales, Marketing
· Assisting the Head of Medical Affairs to ensure that all SOPs relating to the Medical Affairs function are updated on a regular basis.
· Deputising for the Head of Medical Affairs
· Such other dutiesas the management may from time to time reasonably require.
EXPERIENCE & QUALIFICATIONS
· Degree in Pharmacy and a registered UK pharmacist. [Mandatory]
· Experience in the Pharmaceutical industry within Medical Information or Drug Safety (or within a Medical Communications environment).
· Knowledge of ABPI Code of Practice and/or a member of a Drug Information association.
PROFILE OF THE CANDIDATE
Technical skills and abilities
· Knowledge of ABPI Code of Practice.
· Ability to act as Superintendent Pharmacist
· Excellent communication skills (both spoken and written).
· Ability to analyse and understand scientific/medical information and communicate this effectively to internal/external customers.
· Awareness and understanding of drug development pharmaceutical industry practices.
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 daysofyour 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 CL23672 in all correspondence.
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| Job Type |
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Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
ASAP |
| Contact Details |
|
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| Job Title |
|
Recruitment Consultant |
| Location |
|
England, UK |
| Job Number |
|
123219306 |
| Posted |
|
08/02/2012 (09:30) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
CK Clinical has an opening for a recruitment consultant to join their team based in Stevenage. This is an excellent opportunity for a recruiter with a proven aptitude for business to join one of the leading companies in its field.
Since being established in 2004 CK Clinical has grown into one of the most respected and leading UK recruitment companies for Clinical R&D staff and is part of the larger CK Group. Due to continued growth in key business areas and the award of several new preferred supplier agreements with some of the world's largest Pharmaceutical companies, a new opportunity has arisen to join us.
As an independent specialist recruitment company for the pharmaceutical industry, we help recruit well-informed, qualified and motivated candidates for permanent and contract positions across the UK and Europe.
We believe our staff are our greatest asset and have a track record of training, retention and development which is second to none.
We have a strong client list and a reputation of being a fair and transparent recruitment company. This is an exciting opportunity for someone who wants to build on their recruitment career, with a company that upholds the highest standards and that will recognise and reward your hard work and efforts.
If you want to work for a company that stands for honesty, integrity, ethical business practices and success, CK Clinical are the employer of choice. If you want the opportunity to move to the next level CK Clinical are also the employer of choice!
Requirements:
Work experience (e.g. student placement) in a sales environment is essential
Computer literate in Word and Excel
Excellent communication skillsincluding ability to modify communication style to suit situations
Excellent influencing skills including the ability to overcome objection
Able to meet and interact positively and confidently with new and varied people
Able to listen actively, ask questions, clarify points to check understanding
Prioritises objectives to make best use of time and resources Testimonial from a CK Clinical employer (Meera Pattni):
"I joined the team here at CK Clinical in November 2009 after graduating in July with a degree in Bioscience. The work itself can be very challenging, but this makes it very interesting as each day is different and I have thoroughly enjoyed my time so far. I get to speak with people from all different walks of life and learn about their experiences and skills. It is a very rewarding feeling knowing that the work I am doing is making a positive impact on peoples lives. CK Clinical are a great team towork with, everybody gets on really well and we all help each other out as much as we can. I have already learnt so much about the industry and look forward to the challenges and experiences that I will face in the future with the support of my colleagues."
An excellent basic salary and commission package is available together with relocation assistance required.
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 CL22441 in all correspondence.
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| Job Type |
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Permanent |
| Contract Length |
|
N/A |
| Start Date |
|
Negotiable |
| Contact Details |
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| Job Title |
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Clinical Programme Manager |
| Location |
|
London |
| Job Number |
|
120249870 |
| Posted |
|
07/02/2012 (16:20) |
| Agency/Employer |
|
CK Group (Science, Clinical & IT) |
| Description
|
|
Clinical Programme Manager
Permanent
London
Excellent salary and benefits
Description:
A permanent role based at the EU Headquarters of a very successful, global pharmaceutical company. You will provide leadership and direction to Study Managers for the execution of global studies spanning all phases and across a number of therapeutic areas. This will involve the management of third party suppliers and a cross-functional clinical team to ensure that projects adhere to ICH-GCP guidelines and are on schedule and on budget.
Other duties will include:
- Preparation of clinical study protocols, ensuring that their design meets study objectives
- Direct supervision of Study Managers, staff selection and assignment, training and performance reviews
- Management of study budgets and of third party suppliers
- Review and assistance in the preparation of trial documents such as Investigator Protocols, INDs, Clinical Study Reports and MAAs
Requirements:
Strong clinical trialsexperience gained within pharmaceutical companies and / or CROs
Management of third party vendors
Proven line management skills
Preferably with experience of global clinical operations
CK Clinical is an Equal Opportunities employer and welcomesapplications 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 CL23669 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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Electrical Engineer - I&C, Chemical, Norfolk |
| Salary/rate |
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£30000 - £40000/annum |
| Location |
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Norfolk |
| Job Number |
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120249864 |
| Posted |
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07/02/2012 (16:03) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Electrical Engineer - I&C, Chemical, Norfolk. Our client is a world leading Chemical Manufacturer, who is at the forefront of chemical Research, Development & Manufacturing. They are currently looking for an Electrical Engineer to join their ProjectEngineering Team based at their site in Norfolk.
As an Electrical Engineer, you will be responsible for working on Electrical, Instrumentation & Control Systems for use in their busy chemical manufacturing facilities.
Your duties will include project management of Electrical & I&C System projects; carrying out electrical design including performing on-site verficiation to check systems are fit for purpose; use of programmable controllers (PLC & SCADA) as well as completion of all design, quality & industry documentation.
Types of Instrumentation & Systems you will work with will include:
- Low Voltage Electrical Systems (MCCs and 400V Power Distribution)
- Process Instrumentation
- Control Systems for Process Automation & Safety
- Programmable Controllers - PLC & SCADA
This is an outstanding opportunity, which will see you working with a leading name in Chemical Manufacturing. In return they offer a competitive salary and excellent benefits.
To be considered for this role, you will have a qualification in an Engineering discipline (or equivalent) and demonstrated experience working with Instrumentation and/or Control Systems within the Chemical or a related industry.
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 ST23675 in all correspondence.
Keywords: engineering jobs, electrical engineer, instrumentation, control, chemical, Norfolk
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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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Chief Operating Officer (COO) - Diagnostics |
| Location |
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Cambridge, Cambridgeshire |
| Job Number |
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120249856 |
| Posted |
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07/02/2012 (15:40) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Chief Operating Officer (COO) - Diagnostics. Our client is an international Medical Device organisation, specialising in the development & manufacturing of industry changing Molecular Diagnostic Technology. They are currently looking for a Chief Operating Officer (COO) to be based from their site in Cambridge.
As the Chief Operating Officer (COO), you will be responsible for planning, developing & implementing strategies across operational management & development including management of internal operations encompassing commercial manufacturers, supply chain, logistics, materials management & technical support to customers.
Your duties will include:
- A key member of the Executive Leadership Team liaising with other Directors & Managers, coupled with leading, managing & developing Operations Team.
- Lead, drive and manage the development and evaluation of the Company operational strategy and performance.
- Establish and maintain appropriate systems for measuring necessary aspects of operational management and development.
- Monitor, measure and report on operational issues, opportunities, development plans and achievements within agreed formats and timescales.
- Maintain awareness & knowledge of operational best practice to achieve company goals.
- Represent the company at meetings with external parties, customers & at industry events / conferences.
This is an outstanding opportunity to join a growing Diagnostic organisation, which in return offers a negotiable salary & benefits package.
To be considered for this role, you will have a Degree / PhD in a Life Science or Engineering discipline (or equivalent) and:
- Proven track record of growing R&D / Medical Device companies.
- Working knowledge of the Medical Device and/or Diagnostic industries.
- Extensive experience of developing & implementing operational strategies (e.g. Manufacturing, Supply Chain, Logistics).
- Demonstrated commercial experience.
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 ST23651 in all correspondence.
Keywords: science jobs, Chief Operating Officer, COO, diagnostic, medical device, Cambridge
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Permanent |
| Contract Length |
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N/A |
| Start Date |
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Negotiable |
| Contact Details |
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Laboratory Technician, Temp, Food |
| Salary/rate |
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£10 - £11/hour |
| Location |
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Gloucestershire |
| Job Number |
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120249855 |
| Posted |
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07/02/2012 (15:39) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Laboratory Technician, Temp. Our client is a global nutritional company who are currently looking for a Laboratory Technician to join their team of analysts carrying out testing on nutritional drinks.
You will have previous laboratory experience in stability work, HPLC, UPLC and wet chemistry techniques including titrations and pH measurements. You will be providing additional support and after initial training you will be required to work independently within the team.
The working hours are Monday to Friday with the possibility of some overtime.
You will be educated to degree level (or equivalent) in a Chemistry or related subject, with some technical and fault finding experience essential.
This is a contract role for 3-4 months with the possibility 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 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 ST23674 in all correspondence.
Key words: HPLC, UPLC, chemistry, nutritional
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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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February 2012 |
| Contact Details |
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| Job Title |
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Chemist - Temp, Environmental |
| Salary/rate |
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£13000 - £18000/annum |
| Location |
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London |
| Job Number |
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120249838 |
| Posted |
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07/02/2012 (14:06) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Chemist, Temp. Our client is an Environmental company looking for a Chemist to work on a 9 month contract basis.
The responsibilities will include sample preparation and analysis of water, wastewater, sewage, sludge and associated material. Analytical duties may include analysis for metals, nutrients, pH, conductivity, hardness, BOD, COD, TOC, anions, suspended solids, absorbance/transmittance, trace organics and repair/calibration of portable gas monitors. It is essential you have experience with analytical techniques which may include HPLC, GC, LC-MS, GC-MS, ion chromatography, gravimetric, fluorescence and spectrometric analysis, titration, chemiluminescence and use of BOD robot.
Once trained, you will be working unsupervised, organising your own workload to meet deadlines and take responsibility for the day to day running of analyses and allocated tasks.
You will possess a degree (or equivalent) in a Chemistry related subject and must be able to work unsupervised within a team. The person needs to be methodical in approach and have good communication, organisation and numerical skills together with an ability to handle multiple priorities and work accurately.
This is a temporary role for 9 months.
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 ST23671 in all correspondence.
Keywords: Chemist, Chemistry, analytical, HPLC, environmental
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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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April 2012 |
| Contact Details |
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| Job Title |
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Technical Writer - Report Writing, Chemicals |
| Location |
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North West England, North West |
| Job Number |
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120249802 |
| Posted |
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07/02/2012 (11:34) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Technical Writer - Report Writing, Chemicals. Our client, a manufacturer of colours and additives for the polymers and plastics industry, is currently looking to recruit a Technical Writer to join their technical department in the North West.
Themain roles and responsibilities of this Technical Writer will be to assist the technical department with the efficient procurement of raw materials and successful product formulation and analysis in order to maintain and grow sales whilst supportingthe transition to Operational processes. Specifically the department is responsible for: Maintaining and improving the output of the Formulations function; Minimising the impact of New Product Introduction on Operations processes; Providing a qualityanalytical service to support sales functions; Reformulating projects which are supportive of Operational processes; Procurement of raw materials; All quality functions; Testing raw materials; Investigation of customer complaints.
The main purposeof this Technical Writer role is managing and interpreting Non Conformance Report (NCR) data in order to produce concise and professional reports which will be communicated directly to customers and relevant parties involved; Producing and distributing timely, concise and accurate NCR reports to all relevant parties; Management of NCR data in Oracle and Excel databases; Raw material regulatory data management; Collating NCR data from relevant sources and interpretingand summarising this data fortechnical reports; Presenting NCR findings in a concise and professional manner; Producing monthly report summaries of NCR activities, highlighting key issues and trends; Liaising with Procurement Team and directly with suppliers to ensure raw material regulatory information is accurate and validated; Managing raw material regulatory system to ensure compliance with Global policy; Support Technical and Operations Teams with any project work as required; Work together with Operations supporting them regarding MSDS documents and risk assessments.
In order to be considered for this Technical Writer position you will be degree qualified or equivalent in an appropriate, literary subject. With experience of commercial exposure and complaint report writing, you will alsol have exquisite report writing skills and will be able to use word processing and spreadsheet programmes with ease, as well as being able to interpret data so that it is commercially presentable. This role will be approximately 80% desk based and strong IT skills are required. Experience of technical report writing is essential for this position, as is experience in data interpretation and analysis. Knowledge and understanding of global regulatory chemical information would be a strong advantage. You will have excellent verbal and writtencommunication skills and the ability to communicate with at all levels of the organisation. Knowledge of plastics legislation and the plastics industry would be advantageous. Any knowledge of Six Sigma methodology would be beneficial.
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 applicationfor 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 EEA is essential. Please quote reference SH23670 in all correspondence.
Keywords: chemistry jobs, complaint report writing, complaint reporting, technical writing, chemical writing, technical writer, report writing, technical coordinator
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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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Microbiologist |
| Salary/rate |
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£20000 - £22000/annum |
| Location |
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South Wales, Wales |
| Job Number |
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120249788 |
| Posted |
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07/02/2012 (11:01) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Our client, a world leader in laboratory services is looking to recruit a microbiologist to work at their site in Wales on a permanent basis.
The Microbiologist is responsible for Bioburden testing aseptically manufactured products to ensure sterility and to identify the source of any organisms.
- LAL testing of products
- To assist Quality Manager in all aspects of Microbiology.
- To keep lab in neat and tidy fashion.
- To conduct weekly environmental monitoring of clean rooms and trend results.
- To help maintain clean room discipline
The ideal candidate would be qualified to degree level in microbiology or equivalent and have experience of microbiology in a laboratory environment.
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 SH23442 in all correspondence.
Keywords: science jobs, laboratory jobs, microbiology, endotoxin, bioburden, LAL, clean room, autoclave
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| Job Type |
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Permanent |
| Contract Length |
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N/A |
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ASAP |
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Senior Regulatory Officer |
| Location |
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West Yorkshire |
| Job Number |
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120249786 |
| Posted |
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07/02/2012 (10:53) |
| Agency/Employer |
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CK Group (Science, Clinical & IT) |
| Description
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Senior Regulatory Affairs Officer
Reports to: Principal Regulatory Affairs Officer
Main responsibilities: - Collate documents and prepare marketing authorisation applications. - Prepare packaging in line with EU regulatory guidelines, submissions to external databases and liaising with user test teams. - Preparation of type I and II variations. - Assessment of PSUR data. - Licence preparation, national, MRP and DCP. - Prepare, review and submit CTAs.
Benefits include: - Bonus scheme. - Incentive scheme. - Discounted gym.
Person specification: - Prior experience within regulatory affairs required. - Knowledge of CTAs and MAAs. - Ability to prioritise workload. - Problem solving ability. - Attention to detail.
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 CL20701 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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