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. ...
Ideally you will currently be managing UK and European brands and manufacturers within the personal care, cosmetic and toiletry industry selling a variety of raw materials, chemicals, actives or fragrance. You will manage existing clients both in UK and Scandinavian countries as well as looking for new business, manage the sales forecasts, turnover, profit and general customer requirements. You will travel throughout Europe to ...
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...
Organisation Description My Client, based at their modern state of the art manufacturing facility in North London, are seeking a graduate calibre Customer Care Administrator (CCA) to join their team. They are the country’s leading specialist in autologous regenerative medicine, offering cutting edge treatments for cartilage and bone defects. Job Description<...
An opportunity for a medical writer who can demonstrate a high level of knowledge in Virology with an emphasis on the development of promotional and medical education projects in HIV. It is an opportunity for a writer who wants to take the step to senior medical writer . As senior medical writer you will be a key member of the team taking responsibility for the guidance of junior writers, attending client and fa...
Overview: An opportunity for a medical writer with at least 5 years experience wanting to step up and mentor junior writers at a fast growing and fun MedComms agency. You’ll be responsible for the development of promotional and medical education projects. A good knowledge of the RA therapy area is required. You’ll attend client and faculty meetings providing scientific and strategic input. As a senior member of...
Job Description Job Purpose Writing, processing and approving product specifications. Frequent interactions with suppliers on technical issues. Some interaction with customers on technical issues relating to specification. Role Accountabilities: Responsible for co-ordinating all information for new product specifications and transferring data into sp...
Organisation Description My Client, based at their modern state of the art manufacturing facility in North London, are seeking a graduate calibre Customer Care Administrator (CCA) to join their team. They are the country’s leading specialist in autologous regenerative medicine, offering cutting edge treatments for cartilage and bone defects. Job Description<...
Business Modeller / Modelling Consultant c £35,000 - £50,000 negotiable dep on experience Central London Our client is a leader in its field with an established history of applying Operational Research expertise to operational, tactical and strategic issues. As a consequence of significant project demands, there is an immediate need for a Business Modelling Consultant to lead Busin...
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...
Who is this job for? A senior medical writer with experience of manuscript development and publication planning. Who is the job with? The healthcare practice of a global communications business. What's on offer? Your choice to either: work as a writer and continue as such or progress toward an editorial director role ...
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...
Job Description Job purpose To ensure the safety, legality and quality of all new and existing products produced by the company in a timely manor. Liaising with the customer technologists and all other parties involved in the development of new products whilst also assisting in the maintenance of the Technical and Quality systems. Main Duties Facilitat...
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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...
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Date: 28 April
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North London, London
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£24,000 - £28,500 per annum, negotiable, inc benefits
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73 applications
R&D Development Chemist North London Circa 25-28k Type: Permanent Req: Min 3 years experience in analytical method development in the pharma industry. Dep: New Product Development Team Purpose: Duties will include working in the lab on new product development and method development projects. Key Responsibilities: Develop and validate analytical proced...
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...
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Date: 25 April
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North London, London
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£30,000 - £40,000 per annum, negotiable, inc benefits, OTE
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4 applications
Area Sales Manager - Microscopy/Life Sciences - Northern Home Counties, N.E. London to East Anglia - up to £40k plus benefits Leading system solution provider in Microscopy requires an Area Sales Manager to sell their products in to Life Science research laboratories from East Anglia to North East London. The purpose of this role is to maximise profitable sales opportunities and distribution within existing and new customers th...
Are you a graduate looking for a career as an analyst? We are currently recruiting for a charity fundraising call centre in London that needs passionate graduates who want to build a career in the industry. This is an exciting opportunity to join a rapidly expanding company where you will have a direct influence over the key decision makers in the company. You will be working closely with the Operations Director and Fu...
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...
