My client seeks to deliver truly innovative and life-changing drugs for their patients. Their mission is to build a major global biopharmaceutical corporation while focusing on the discovery and the development of products for the treatment of cancer and other severe, immune, inflammatory conditions. They are currently recruiting for an Oncology Regulatory Manager to work a 12 month Fixed Term Contract at their offices in Uxbridge. ...
Regulatory Affairs Specialist - REACH - Toxicology - Eco toxicology - Pharmacology - Cosmetics / Personal Care - London - Permanent - £30-35K + Benefits An international leader in the Cosmetics and Personal Care market is currently seeking to appoint a Regulatory Affairs Specialist to work as part of the groups Compliance Division, Product Safety and Regulatory Affairs Dept. based in West London. You will need to...
The Company: A global biopharmaceutical company involved in the discovery, development & commercialisation of treatments for severe conditions. They currently have hundreds of clinical trials active globally focusing on mostly incurable conditions. They employ thousands of people world wide and has grown to this size from relatively humble beginnings over 30 years ago. The Role This is a new role that wi...
We are currently working with a medium sized pharmaceutical company, who are looking for a new and experienced Qualified Person / QP to join them, working out of their offices in West London The person we are looking for has somewhere in the region of 2 - 4 yrs post certification experience as a Qualified Person. This position has come about as the current Qualified Person / QP, working flat out and needs&n...
Job Description To be responsible for handling sales enquiries received into sales office for BLS (Biological and Life Sciences) related products for UK managed territories ensuring orders are processed and entered within agreed timescales. To provide administrative support to the Product Specialists and Field Sales staff. To respond to and satisfactorily deal with communication received from customers via all ch...
Job Description To be responsible for handling sales enquiries received into the sales office for controlled drugs orders, ensuring import/export licences are applied for which satisfy Home Office regulations and legal compliance and are within agreed time scales to satisfy customer expectations. To ensure continuity deputise the orders desk in the absence of the Sales Administration Manager.. • To ensure ...
Job Description To be responsible for handling sales enquiries received into the office for products for Ireland and overseas countries. Ensuring orders are processed and entered onto database within agreed timescales. To provide administrative support to the Product Specialists and Field Sales staff. • Raising quotations, pro-formas, orders, Giving product information to customers. • Assisting with the mainten...
Hertfordshire Medical Device exprienced Quality Assurance Officer- 28-32K per annum Our client is a highly reputed and a very well established Medical Device business. They are an accredited ISO 13485 site, based in Hertfordshire. From very humble beginnings back in 70s they currently employ several thousand employees across EU, The US, Asia, the Mid East, Far East and Americas. A world class global employer their name resonates in ...
We currently recruiting for several vacancies as a Production Technicians to work on on our nightshift, dayshift and 12hour shift, 4days on 4days off. Dayshift - 6am-2pm, 2pm-10pm weekly rotating shift. Nightshift - 10pm - 6am We are looking for candidates, who ideally must possess a relevant degree, wishing to develop their career within a pharmaceutical environment. Training will be provided for the right ca...
Duties will include liaising with clients, setting up new projects on computer system, tracking projects being completed and recording results of investigations, preparing detailed client reports and maintaining client files. This vacancy is based in the United Kingdom. A fundamental part of our service is that you will be required to make a personal visit to our office to finalise any application made on-line.&nbs...
Your job duties will be as follows: - Undertake tests and experiments according to scientific protocol and procedures, including sample preparation for over 1000 assays, including Urine, CSF, Histology, Serum, Plasma, body fluids, EDTA whole blood and Lithium heparin. - Responsible for input, analyses and reporting of results and experiments for Referrals assays and packaging of all referred samples to the HPA reference laborat...
You will be responsible for a team in the laboratory that receives, aliquots, separates samples entering the laboratory for all disciplines including Cytology, Haematology, Chemistry/Endocrinology, Virology/Immunology, Microbiology, Cytogenetics or any other research site. Your job duties will be as follows: - Oversee a team who is responsible for the preparation of all STAT samples by centrifugation, plasma/serum separation a...
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Date: 2 May
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Hammersmith, London
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£25,000 - £30,000 per annum, negotiable, inc benefits, OTE
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64 applications
For more than 20 years this company has focused on the development and manufacturing of high-quality recombinant cytokine products for life-science research. Now a world leader in the production of E.Coli, insect and mammalian cell-derived recombinant proteins, and ELISA development kits and other cytokine-related reagents. This is an exciting opportunity for a European Sales Executive, based in the heart of Greater London. Ke...
We are working with a leading generic medicine company, based in West London, who are looking for a Quality Person to join their expanding UK business. As the Qualified Person. working with the Senior QP, you will assist in the certification of every batch of medicines before release to the EU market. You will have completed a period of at least four years of theoretical and practical study in one of the following s...
Our client is one of the largest providers of global central laboratory services offering testing services to companies running clinical trials. With central laboratory facilities in North America and Europe and alliance laboratories in China, Singapore, Australia, and South America, investigative sites are supported in over 4,000 cities across 60 countries. We are currently seeking to appoint a Project Associate to support Project M...
Pharmacovigilance Officer DUTIES AND RESPONSIBILITIES (NOT LIMITED) Knowledge and use of the Pharmacovigilance database for processing of Adverse Events and Adverse Drug Reactions. Literature searches and obtaining literature articles and reviews. Submission of AEs and ADRs in the appropriate format to the Regulatory bodies, in compliance with the statutory timelines. Organisation of all ca...
Senior Biomedical Scientist - Haematology/Blood Transfusion Fixed Term Contract - 8 months Maternity Cover Competitive base salary plus shift allowance/on-call payment Hours: Monday to Friday (9.00am - 5.30pm), participating in shift/on-call rota, weekend work and bank holidays. We currently have an exciting opportunity for a Senior Biomedical Scientist to join our client’s busy Haematology departme...
Quality Systems Data Document Processor - Hertfordshire Opportunity : This job opportunity is for all the quality assurance systems documents controllers out there looking for a new position. This is a brand new potion that has become available for a growing medical device / pharmaceutical company. Your role as Quality Assurance Systems Data Document Processor / Controller based in Hertfordshire...
This new and exciting opportunity for an outstanding Quality Engineer will mean you working closely with the Quality team, suppliers and manufacturing to provide a top class Quality Engineering capability for the business. Focussing particularly on ground breaking innovative new products, utilising plastic moulded components you’ll be involved with supplier development activities to establish the specifications and acceptan...
Medical Writer - Marlow, Bucks or London W4 - Competitive Salary + Benefits This is a permanent opportunity for a Medical Writer to be based at the offices in Marlow, Bucks or London W4. You will be responsible for (a) researching and developing technical material, (b) ensuring that all output adheres to written brief, is accurate in content and editorial style and can be referenced, (c) liaisin...
Our client is one of the largest providers of global central laboratory services offering testing services to companies running clinical trials. With central laboratory facilities in North America and Europe and alliance laboratories in China, Singapore, Australia, and South America, investigative sites are supported in over 4,000 cities across 60 countries. We are currently looking for an experienced Team Manager to lead, coach and ...
JOB DESCRIPTION - Medical Writer Reporting to : Associate Divisional Director Principal Role: You are responsible for (a) researching and developing technical material, (b) ensuring that all output adheres to written brief, is accurate in content and editorial style and can be referenced, (c) liaising with clients and key opinion leaders on content development either through th...
Want to work for one of Britain’s Top Employers of 2011? Working Hours: Monday- Friday, 30 hours per week, plus participation in the Saturday rota (1 weekend in 3). Based on independent research by the CRF Institute, our client has been certified as one of Britain's Top Employers 2011 for the fourth year running for its outstanding HR Policies and excellent working conditions. An exciting opportunity has arisen fo...
Want to work for one of Britain’s Top Employers of 2011? 9 Month Fixed Term Contract Based on independent research by the CRF Institute, our client has been certified as one of Britain's Top Employers 2011 for the fourth year running for its outstanding HR Policies and excellent working conditions. An exciting opportunity has arisen for an HPC registered Biomedical Scientist to join the organisati...
Our client is one of the largest providers of global central laboratory services offering testing services to companies running clinical trials. With central laboratory facilities in North America and Europe and alliance laboratories in China, Singapore, Australia, and South America, investigative sites are supported in over 4,000 cities across 60 countries. Based on independent research by the CRF Institute, our client has also ...
