Nonstop Recruitment is working with a number of Contract Research Organisations, Industry companies and Consultancies across the UK who are searching for those who specialise within Environmental Fate. We therefore seek those who specialise in Fate, or Environmental Risk Assessments and would be interested to speak with you even if you are not actively looking to move The positions on offer vary from highly experience Environmental F...
Regulatory Affairs Consultant Would you like to join a dynamic global Regulatory Affairs team and work on exciting projects? My client is looking for a new member of their Regulatory group. They are looking for an experienced pharmaceutical regulatory affairs professional who loves to manage projects Do you possess the following skills? - Pharmaceutical industry regulatory Affairs experience is an ab...
Business Development Executive - Ideally suited for a candidate with an Environmental background Our client is an established Contract Research Organisation with a proven history within offering testing and regulatory consultative services. Due to recent mergers they now offer one of the largest environmental services in the world. Consequently, you will be in a position where you can utilise your environmental background to promote ...
Regulatory Project Leader - Agrochemicals Crop Protection plant protection Our client is an established and global enterprise with a focus on specialised chemicals and agrochemical products. As the leading producer of products within their chosen industry, you will be applying to a company with a phenomenal brand image that has the reputation for being the best. Association with such a company will contribute positively to your c...
We have an exciting opportunity for a Bioassay Specialist to join a leading biopharmaceutical company based in the North West of England. ROLE OVERVIEW: The Bioassay Specialist will support/work with the Analytical Molecular Biology Team Leader and the process development and manufacturing groups throughout the product lifecycle by utilising your extensive scientific knowledge of in vitro bioassays for the analysis of biol...
European Regulatory Specialist Biocides and REACh - 12 Month fixed term contract Our client is a global leader in microbial control and surgical equipment sterilisation. They aim to prevent infection and have a well known brand image of being one of the first providers to market on many product ranges within microbial control. As a Regulatory Specialist in a 12 month contract, you will work to EU regulations an...
Regulatory Project Leader - Agrochemicals Crop Protection Our client is an established and global enterprise with a focus on specialised chemicals. As the leading producer of products within their chosen industry, you will be applying to a company with a phenomenal brand image that has the reputation for being the best. Association with such a company will contribute positively to your career progression and professional developm...
Job Description Job Purpose To act as a therapy area expert and provide a quality first line medical information service to the UK and Ireland and expert second line support for affiliates across Europe. To provide a quality information service on products to internal stakeholders To promote the safe and effective use of products by ensuring accurate, balanced and current information is...
Product Specialist - IVD's (Dutch speaker) In-vitro Diagnostics Office based from South London This is an excellent opportunity for an experienced biomedical scientist or field application support scientist/product specialist to join a leading diagnostics organisation. Working from the companies South London offices you will be responsible for supporting their market leading IVD products t...
Business Process Project Manager, Cambridgeshire, Negotiable Salary + Bens An excellent opportunity for a highly motivated and personable communicator who is interested in continuous improvement and business process efficiency. Your role will be to work with different departments at a scientific research company and help them improve processes and efficiency. Ideally you will have a scientific background, an unde...
For this job, we are seeking a scientist with experience of manufacturing in the Biotechnology industry. You will be responsible for providing technical support for downstream processing of biopharmaceutical products. This job will involve lab to pilot plant optimisation of processes, specifically developing processes for manufacture of large molecules via a fermentation process in a highly automated cGMP manufacturing environment. Experien...
Job Description: Our client is looking for a talented copywriter to join their expanding healthcare advertising agency. This person will be working across a number of accounts and it is a great opportunity to inspire existing clients and to develop new business. Candidate Requirements: A track record in healthcare copywriting, a science background and an understanding of our industry is essential. Solid sale...
Laboratory Solutions are looking to recruit a Research Scientist for a molecular biology based SME in Cambridge. A successful candidate for this temp to perm role must be able to start NEXT WEEK The following techniques are of interest- molecular biology, immunology, genetic engineering, protein chemistry and tissue culture. The work will involve cloning and expression in mammalian and yeast cells, antibody purification and an...
170 jobs matching this search were posted in the last week
My client are a world leader in pharmaceutical manufacturing. They are currently looking for multiple process organic chemists to join their successful team in Cheshire as part of a 6 month temporary contract. The Role: You'll be responsible for scaling up to 100 grams (small scale), You'll act as a key part of the organic and process team, You'll be responsible for small scale synthesis of organi...
Job Description: We are assisting our client, a medical communications agency, in finding a medical writer to be based in Cheshire. The medical writer will work within a respiratory team which includes a number of therapy areas (e.g. asthma, COPD, PHA). There will be a full and varied workload, including publications-related work, meetings (advisory boards, symposia, masterclasses), multi-media deliverables, etc. <br ...
This is an exciting opportunity to join an Oxfordshire based Biotechnology company working as a Product Manager Next Generation Sequencing. The key responsibilities of the role include but are not limited to: Owning the marketing process and delivering marketing plans to achieve revenue goals. Develop successful action plans to maximise sales Develop a strong network understanding needs and feedback and de...
Job Description: Our client is a medical communications company in London seeking an experienced Senior Medical Writer. The successful candidate needs to be able to consistently produce high quality materials for the pharmaceutical industry and other medical bodies. Global and national travel will be a requirement for this role. The Role: • Researching and developing a range of medical educa...
Job Description: We are assisting our client in recruiting a Senior Clinical Research Associate. This is a permanent position office based in Cambridgeshire. Under limited supervision, the Senior CRA monitors and oversees clinical practices for one or more multi-site clinical trials, ensuring compliance with all regulatory agency requirements. Maintains sound clinical practices to ensure validity of study. Monitors the cond...
Process Development Manager (Personalcare) Ref : 17950 Our Scottish based client is actively looking for a Process Development Manager to lead and establish new product development formulations from lab to manufacture. Additional duties will include:- - Managing R&D labs and Process room to bring products to manufacture in a timely manner - Managing and improving the NPD processes on site - Ensurin...
Organisation Description Reed Scientific are currently recruiting a Quality Assurance Engineer for a market leading manufacturing operations in Port Talbot. The holder will be responsible for management and administration of the customer complaints system to ensure that timely and appropriate investigations are conducted and high quality feedback is provided to the customer. He / she will be responsible for developing...
Organisation Description Reed Scientific are currently recruiting a Quality Assurance Engineer for a market leading manufacturing operations in Port Talbot. The holder will be responsible for management and administration of the customer complaints system to ensure that timely and appropriate investigations are conducted and high quality feedback is provided to the customer. He / she will be responsible for developing...
A Medical Device Auditor is required for a UK Notified Body, this role will be home based but you will be expected to travel extensively to carry out audits and Medical Device companies across the UK. You must have experience of working with sterile devices and carrying out a technical review of all documentation and files related to the products. You will have an excellent understanding of Medical Device Directive 93/42/EEC. The role is pa...
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Date: 2 May
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Germany,
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Competitive salary
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1 application
Job Description: Our client is a top international CRO who are seekign a Data Operations Lead for their Berlin office to take overall accountability on the execution of Data Management and Biostatistics services on Early Phase and Early Product Development projects. The DOL is the single point of contact for the client and coordinates project setup, execution and close out. He or she works with Clinical Data Pro...
Job Description: Our client is a growing CRO who are seeking a Senior Medical Writer in their Berkshire offices. Summary Researches, creates, edits, and coordinates the production of clinical documents such as study protocols and consent forms, clinical study reports and Investigators’ Brochures. Provides writing support for more complex clinical documentation and works with project managers, data managers, statisticia...
Job Description: We are assisting our client in finding a Senior Specialist for their Phase I unit in North West London. The post holder will provide guidance on requirements for the conduct of clinical trials including: • Maintain drug accountability records in accordance with agreed protocols and the principles of International Conference on Harmonization Good Clinical Practice (GCP) and Good Manufacturing Practice (...
