World Science Jobs

Lecturer (Non Clinical) in Clinical Chemistry – Liverpool

School of Clinical Science
Unit of Clinical Chemistry

You will carry out independent and collaborative research in Clinical Chemistry and Metabolic Medicine, generate research income and contribute to the teaching of Clinical Chemistry at both the undergraduate and postgraduate levels. The Department’s major interests centre around immunoassay development, HPLC, Tandem MS, ICPMS, bone metabolism, endocrine biochemistry and nutrition.

You will also perform Clinical Scientist duties related to an area of specialist interest within the NHS Department of Clinical Biochemistry and Metabolic Medicine, Royal Liverpool and Broadgreen University Hospitals Trust.

Job Ref: A-501964/NS
Closing Date: 3 November 2008

For full details, or to request an application pack, visit www.liv.ac.uk/working/job_vacancies/ or e-mail jobs@liv.ac.uk

Tel 0151 794 2210 (24 hr answerphone)
Please quote Job Ref in all enquiries.

COMMITTED TO DIVERSITY AND EQUALITY OF OPPORTUNITY

Our client is a specialty pharmaceuticals company utilising proprietary drug delivery and formulation technologies to develop and commercialise small molecule drugs to treat pain and neurological conditions. They now have an immediate vacancy for an experienced formulation analyst to support a small dynamic development laboratory within a new facility based in Bath The candidate will be expected to develop the laboratory’s analytical section: develop and refine HPLC drug assay and related substances methods; generate and help interpret results; and support the work of the formulation team. They are a small team so flexibility and the ability to work independently are essential.

Applicants must have a science-based degree and have extensive practical analytical experience working in the pharmaceutical industry. In addition applicants must have at least 2 years method development experience.

General Requirements:

- Experience of operating HPLC hardware and software and interpretation of data generated
- Experience of maintaining and troubleshooting HPLC and UV systems
- Experience of developing and validating HPLC methods for pharmaceutical development
- The ability to design experiments to support product development work
- Experience of working within the pharmaceutical industry
- Experience of standard pharmaceutical testing techniques such as dissolution, disintegration and particle size analysis
- Knowledge of ICH guidelines, MHRA and/or FDA regulatory requirements
- Experience of developing analytical method for combination therapies
- Experience of running stability studies to support regulatory submission
- Experience of working in a GLP or GMP laboratory including the preparation of reports and SOPs
- A good understanding of the product development process with respect to analytical method development and testing to support clinical trials.

key words: “analyst” or “analytical chemist” or “analytical scientist” or “qc chemist” or “qc scientist” or “quality control chemist” or “quality control scientist” or “laboratory technician” or “analytical development chemist” or “analytical development scientist” or “stability chemist” or “stability scientist” or “analytical technician” or “qc technician” or “lab technician” or “method development chemist” or “method development scientist”. Bristol, Avon, Bath, Wiltshire, Dorset, Gloucestershire, Devon

Java/AJAX Software Engineer Cambridge Keywords: Struts, Spring, JUnit, Hibernate, Tomcat. Cambridge based software house are looking for an experienced Java AJAX Software Developer to join their market leading company. Working alongside a first class team of scientists, software developers and software architects, the successful candidate will be concentrating on a variety of projects from developing web services and enterprise applications through to the development of the Oracle backend that supports these applications.

To be successful in this position you will be highly competent at developing Java-based web services with experience with one or more of the following: Struts, Spring, JUnit, Hibernate, and Tomcat. Besides excellent technical skills, the ideal candidate will bring both enthusiasm and the ability to develop high-quality software, you will working closely with Quality Assurance and other development teams to ensure good test coverage of all newly developed functionality.

The ideal candidate will be Qualified to at least degree level in either a computer science or chemistry related scientific discipline.

It is essential that you have solid web application development experience using JavaScript/AJAX. Oracle or PL/SQL expertise would be an advantage, as is good knowledge of C++.

Rewards include a fantastic salary and bonus scheme including Bupa healthcare, travel insurance and contributory pension scheme. The successful candidate will have the opportunity for overseas travel with career progression opportunities and performance bonus. This is a once in a life time opportunity to play a major part in influencing projects within a market leading scientific company

For more information on this role contact Kieron McDaid at Paramount Recruitment on 01216165157

Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.

We are looking for an Analytical Laboratory Supervisor to join a leading Biotechnology company based in the Cheshire area.

Position Purpose:
To have overall responsibility for the analytical capabilities at the company. This would involve managing a team of analytical scientists who are responsible for the rapid and accurate measurement of biological samples using both Liquid Chromatography-Mass Spectrometry (LC-MS) and Liquid Chromatography-Mass Spectrometry-Mass Spectrometry (LC-MS/MS) techniques. In addition to have overall responsibility for the bioanalytical method development and metabolite identification studies performed at the company.

Principal Accountabilities
To manage a team of analytical scientists and ensure all analytical work is performed to the highest standard within deadline
To oversee and take responsibility for the bioanalytical method development studies and metabolite identification studies performed at the company
To continually develop the analytical capabilities of the company
To ensure that equipment/instrumentation is calibrated and records and documentation are maintained

Skills and Competencies
Excellent communication, both internally and externally, and line management skills
Ability to work in a highly pressurized environment and meet multiple internal deadlines
Demonstrated use of initiative and innovation to solve problems and troubleshoot
Able to communicate effectively within a fast-paced team environment to individuals with varying levels knowledge
Routine experience with both MasssLynx and Analyst software

To apply for this position, candidates must be eligible to live and work in the UK

Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy.

Job reference: 182948DXC
Company: Matchtech
Contact name: Darren Compton
Address: 1450 Parkway Solent Business Park Whiteley Fareham PO15 7AF
Telephone: 01489898272
Fax: 01489898782
Company web address: Click here.

AKCDT 13833 Product Safety Toxicologist
· Permanent
· Hull

Have you got experience in Toxicology and/or Product Safety?

Our client, a global force in Household, Health and Personal Care, is looking to recruit a Product Safety Toxicologist to provide support in mammalian toxicology and risk assessment, and their impact across household product categories. The position will involve all safety aspects of consumer products, including classification, labelling and compliance requirements.

Requirments:
· You will ideally have an Msc or PhD in Toxicology or a related discipline.
· Experience in a similar role within a manufacturing/process environment, ideally FMCG, is desirable but not essential.
· Strong communication skills are paramount, as you will be liaising with internal and external contacts, to ensure agreed timescales are met.

Interested in this fantastic opportunity? Please apply on-line or contact Alana Kilkenny for more information on: 0161 868 2205.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.

SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

We are currently looking for a Specifications Technologist with previous experience of specification writing to join a leading food producer in West Sussex.

PURPOSE OF JOB

Role focuses on technical areas of the business with strong emphasis on specifications.

JOB CONTEXT AND CONTENT

The job holder will be the centre of expertise and will manage the customer specification interface with major retailers and others. The job will include responsibility for gathering food specification information from various sources both internally and externally and interpreting / inputting the data such that it matches the requirements of customer specifications.
Contact with all departments and staff at the sites. Regular liaison with customer technical and commercial teams. Provision of a comprehensive specifications service to serve the needs of both customers and internal staff. Regular contact with technical and NPD departments will be required.

PLANNING AND ORGANISING

The Specification Technologist will be required to plan and organise their own time under the general direction of the Technical managers. Deadlines must be agreed and adhered to ensuring a full and comprehensive specifications service.
This will involves liaising with suppliers, customers and staff to ensure that all required information is gathered and that procedures have been followed.
Advice may be sought from TSO, EHO, Food Research associations and Chilled Food Association.

CONTACTS

Internally All staff at all levels particularly technical, NPD and commercial teams

Externally Own label customers, raw material suppliers, Trading Standards Office, Environmental Health Office.

KNOWLEDGE AND EXPERIENCE

Preferably a food related degree or similar with minimum 2 years experience of specification completion within the food industry.
Specific knowledge of some or all of the following specification systems would be ideal: Sainsburys Inspire, Waitrose Ramesys, Co-op LSIQ, Hamilton Grant.
Knowledge of Microsoft Word, Excel and Access is mandatory.

Accountabilities

Implementing and achieving technical specification requirements.
To obtain complete and accurate information from suppliers, technical and NPD teams to allow correct completion of required specifications to agreed deadlines.
Satisfactory and timely completion of set projects.
Provide a comprehensive and accurate specification service within the parameters of the role.
To produce complete concise specifications with documentation as required.
To promote and develop specification procedures and considerations within the business.

To apply for this position, candidates must be eligible to live and work in the UK

Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy.

QC Stability Analyst required to support the UK stability programme. The role will involve conducting the routine activities to support the stability program in accordance with written operating procedures and cGMP; pulling and distribution of stability samples; receiving and logging stability data; drafting and implementing stability protocols and reports in compliance with ICH guidelines.
Suitable candidates will be educated to HND level or equivalent in a related scientific discipline, with previous proven work experience in the pharmaceutical/biotechnology industry, preferably within stability.
Please apply on line or contact Jennie Dempsey on 0161 8682200 quoting ref JD13768.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.

SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

Senior Project Manager (Pharmaceutical Development)- M4 Corridor
£40k – £45k + Bonus + Relocation + Excellent Benefits Package

Are you looking for a challenging senior project management role?

Are you keen to join a leading international pharmaceutical development and manufacturing outsourcing organisation?

An opening exists for a Senior Project Manager to manage team of project managers and project co-ordinators and to oversee a portfolio of client projects for this successful company. The role holder will manage the link between clients and project teams, facilitating the delivery of pharmaceutical development projects. You will outline and monitor key project milestones, ensuring client requirement and objectives are understood and delivered.

You must have a science related degree (or equivilent) plus advanced knowledge and experience in pharmaceutical product development and extensive project management experience. You must have proven interpersonal and communication skills and have the ability to direct a multi-disciplinary project team.

In return, you will gain great experience working in a large expanding company and will have the opportunity to develop your career further. You will also receive a competitive salary and benefits package.

Please apply on-line or contact Neil Walton on 01753 589627 for further information.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.

SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

QC Chemist
Permanent, Full Time
£15,700 basic + £9,400 shift allowance

Our client are a fragrance and beauty company. With 8,500 employees worldwide and offices in 30 countries, they are the largest in their industry.

Skills required:

- Quality control laboratory experience
- Colour matching within the cosmetics industry (other industries will be considered)
- Knowledge of colour formulations (wax, powder based, and emulsion technology)
- Good communication skills
- Self driven
- Strong attention to detail

Location: Kent

Job Description:

- Bulk QC; shade, specifications, stability
- Preparation of colour formulation
- Colour matching and shade development
- Scaling-up; pilots, line trials, and transfers to manufacturing

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency.

SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm.

JOB SUMMARY:

An opportunity has arisen in the formulation department to assist in the development of both topical pharmaceutical (for OTC and ethical markets) and cosmetic products. The position will include laboratory-scale formulation development, the scale-up of potential formulations in our pilot facility, and involvement with technology transfer of development products into commercial manufacture in accordance with GMP. Some travel may be required between sites.

OBJECTIVES AND PURPOSE OF THE POST:

1.1Formulation Development for New and Existing Products

To prepare a range of new product formulations (creams, gels, lotions, shampoos) and monitor them for physical/emulsion stability, pH and viscosity to find the optimum formulation. As part of this development work new materials will require sourcing in-line with current guidelines/directives. Pharmaceutical development reports will require writing and updating for each project.

Formulation Development work will also be required to support and improve Existing Product lines, where necessary. Product line extensions will also be investigated.

1.2Preparing supplies of Development Products for Accelerated Stability Studies

Formulations which have passed the initial screening process will need to be manufactured on a small scale for accelerated stability trials in a range of packaging materials; these will be screened by the analytical laboratory for both chemical and physical stability.

1.3Preparing supplies of Development Products for Stability/Clinical Studies

Formulations selected from the accelerated screening programme are manufactured on a larger scale (up to 100 kg) at our pilot facility at Kempston. The position will include assisting in the dispensing, manufacture and filling of pilot-scale batches for stability/clinical trials. This will involve working to GMP and manual lifting. Data generated from these trials is used for the Product Licence application.

The position will include the labelling and presentation of supplies for clinical trials.

OBJECTIVES AND PURPOSE OF THE POST (cont.):

1.4Environmental Monitoring

On an occasional basis, environmental plates and water sample will require monitoring and reporting.

1.5Data Handling

Ability to use computer software packages, such as LIMS, Excel and Word for processing and reporting of data.

1.6Day-to-Day running of the Formulation Laboratory

Take equal part in the overall running of the Formulation Laboratory, including equipment maintenance, calibration of apparatus and other general duties such as solvent disposal.

1.7To bring to the attention of his/her immediate superior any difficulties or problems encountered in the performance of his/her duties.

1.8To be aware of the safety regulations in operation in the department, and in the light of the Health and Safety at work act, to perform his/her duties in such a manner so as not to endanger the safety and health of his/her fellow workers.

1.9To perform other scientific and technical duties as requested.

SKILLS REQUIRED (after suitable training):

The ideal candidate would have a degree/diploma or equivalent in a scientific discipline. Formulation experience, preferably in pharmaceuticals/cosmetics or other skincare products and an appreciation of working in a GMP environment are required.

GENERAL:

To comply at all times with any regulations issued by the Company, especially those governing Health and Safety at work, and to ensure that any defects that may affect safety at work are brought to the attention of the appropriate manager.

This job description reflects the present requirements of the post. It does not form part of the contract of employment. As the duties of the post change and develop, the job description will be reviewed and will be subject to amendment in consultation with the postholder.

CONFIDENTIALITY:

All staff are required to respect the confidentiality of all matters that they may learn relating to their employment, Company business and other members of staff. All staff are expected to respect the requirements under the Data Protection Act 1998

To apply for this position, candidates must be eligible to live and work in the UK

Formulation, Hertfordshire, GMP, GLP, process, manufacturing

Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy.

• Job reference: 180441SIB
• Company: Matchtech
• Contact name: Simon Birmingham
• Address: 1450 Parkway Solent Business Park Whiteley Fareham PO15 7AF
• Telephone: 01489898247
• Fax: 01489898290