Job Description Main purpose of the job: To provide specialist care focused scientific and technical support to European medical affairs and marketing activities and to support/prepare the launch activities for other products To Design, implement and manage sponsored Phase IV studies and data generation within European markets and coordinate affiliate generated data review and approval process (IIT). <br /...
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...
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<...
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<...
A leading international group of laboratories with about US$ 900 million annual sales and 8,000 employees across 150 sites in 29 countries providing an unparalleled range of testing and support services to the pharmaceutical, food, environmental and consumer products industries and to governments. Now looking to recruit a Quality Coordinator based in Acton, London. Main Duties: - Carrying out internal audits and...
Job Description Responsible for the quality and regulatory compliance for studies in Start-up Phase. Perform SSU Project Team Management activities, coordinate the efforts of SSU Team Members and maintain clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by The Company and its clients. • Organizes efforts of team members assig...
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...
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...
Job Description Responsible for the successful planning, implementation and execution of contracted clinical activity. Assures the accurate transfer of contracts from proposal through project completion. Functionally responsible for all team members throughout the duration of each clinical trial. Assures clear client communication, process documentation, and compliance with Good Clinical Practices and proc...
Job Description Experience required: (1) CDISC, including SDTM. (2) Minimum 5 years working in pharmaceutical or CRO environment. (3) Early phase clinical trials. (4) SAS programming (not just point-and-click programming in Enterprise Guide). (5) Ability to explain what validation involves, and why it is necessary. Job description: (1) SAS program developmen...
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...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplicate...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplica...
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...
Regulatory Affairs Supervisor North London £30 - £35k dependant on experience and qualifications Our client is a successful importer, wholesaler and distributor of pharmaceuticals, generics and branded fragrances. With a growing customer base and increasing product portfolio the Company is now set for further expansion We are looking for an experienced RA Supervisor to be responsible for the...
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...
