EU Dangerous Goods Safety Specialist / DGSA, Leicester, Competitive package + Bens We are looking for a Dangerous Goods Safety Specialist / DGSA to join a global chemical business . Your role will be to ensure the business complies with Directives 2008/68/EC and 2000/18/EC to ensure that adequate / compliant processes for loading, unloading and transport of dangerous goods are in ...
EU Dangerous Goods Safety Specialist / DGSA, Loughborough, Competitive package + Bens We are looking for a Dangerous Goods Safety Specialist / DGSA to join a global chemical business . Your role will be to ensure the business complies with Directives 2008/68/EC and 2000/18/EC to ensure that adequate / compliant processes for loading, unloading and transport of dangerous goods are ...
DESIGN ASSESSOR/MANAGER - HOME BASED UK - SALARY NEGOTIABLE Line Manager’s Position: Clinical Affairs and Regulatory - Senior Manager Job Title: Flexible dep on Experience (DESIGN ASSESSOR/TECHNICAL MANAGER, etc.) Salary: Circa 65k with 20% performance based bonus Type: Permanent Location; Home based in UK, 1-2 days in Office per month & with travel Benefits: Company car, Healthcare, Pensi...
Organisation Description My client, a professional membership body, is looking to appoint an Enquiries Coordinator.They have over 15,000 members and employ around 35 staff. The Professional Development team provides a range of services, including encouraging research, developing professional standards, professional development resources including e-learning. Reporting to the Head of Professional Development...
Organisation Description My client, a professional membership body, is looking to appoint an Enquiries Coordinator.They have over 15,000 members and employ around 35 staff. The Professional Development team provides a range of services, including encouraging research, developing professional standards, professional development resources including e-learning. Reporting to the Head of Professional Development...
Recruiters & Team Leaders - Pharmaceutical / Life Sciences Recruitment - London - 024VS Specialist London based Recruitment Consultancy with international presence in Europe and APAC region is increasing their headcount in their LIFE SCIENCES & PHARMACEUTICAL divisions and looking for consultants and team leaders who have worked across this niche market either recruiting within BioTech, BioMetrics, Clinic...
Do you have experience working in labeling? Are you looking for an exciting opportunity to join a global pharmaceutical company? This is an exciting opportunity to join a global pharmaceutical company working as a Labeling Document Specialist to support products in Research and Development. The main responsibility of the role will be converting labeling documents including core company data sheets and international packa...
Kelly.Diver@kellyservices My client are a leading pharmaceutical company based in West Yorkshire, they are currently seeking a Senior Regulatory Affairs specialist to join their well established team of accomplished scientists. The Role: To Prepare packaging, review against excipient guidelines, Check Packaged items. Braille check and conversant with EU Braille. Liasing with user te...
Aquatic Ecotoxicologist, Suffolk, Negotiable salary + bens An excellent opportunity to join a large established state of the art aquatic ecotoxicology facility that offers a diverse range of indoor and outdoor studies for chemical, agrochemical and pharmaceutical compounds. As Study Director, you will manage and coordinate your own studies from start to finish. Ideally you will have existing aquatic ecotoxicology experience along...
Aquatic Ecotoxicologist, Suffolk, Negotiable salary + bens An excellent opportunity to join a large established state of the art aquatic ecotoxicology facility that offers a diverse range of indoor and outdoor studies for chemical, agrochemical and pharmaceutical compounds. As Study Director, you will manage and coordinate your own studies from start to finish. Ideally you will have existing aquatic ecotoxicology experience along...
Job Description Main purpose of the role: Provide medical affairs support for pre and post launch activities for existing and future Epilepsy BU products in the UK and Eire Provide medical affairs support for local market access activities in the region Take responsibility for key projects at the EMEA level Qualifications, education and language requirements: Medical Deg...
Job Description To provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. Consultancy applicants are to act as a central point of contact for assigned key clients and work with other staff to promote and develop the business. Reed Specialist Recruitment Limited is an employment agency and emplo...
Job Description To provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. To act as the central point of contact for assigned key clients. To work with other staff to develop and promote the business. Reed Specialist Recruitment Limited is an employment agency and employment business ...
14 jobs matching this search were posted in the last week
• Packaging Specialist • Horsham, West Sussex (own transport ESSENTIAL) • Salary: £20k - £24k (depending on experience) • 2 positions available (both Mon - Fri, 1 x core hours / 1 x early shift 6:00 - 2:15) • Based in Business Planning project support team • Experience from a regulated organisation or packaging environment • Strong planning, customer service, attention to detail and administration skill...
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Date: 25 April
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France,
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€55,000 - €70,000 per annum, negotiable, pro-rata, inc benefits
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6 applications
SPINE PRODUCT SPECIALIST - MEDICAL DEVICES - FRANCE Job Title: EU Notified Body Medical Device Product Specialist Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: UK or France Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification Manage a portfolio of ...
SPINE PRODUCT SPECIALIST - MEDICAL DEVICES - UK Job Title: EU Notified Body Medical Device Product Specialist Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: UK or France Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification Manage a portfolio of medi...
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Date: 18 April
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Abingdon, Oxfordshire
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£30,000 - £40,000 per annum, negotiable, pro-rata, inc benefits
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4 applications
SENIOR RA ASSOCIATE - Medical Devices - Oxfordshire - Circa 35-40k Type: Permanent Reports to: RA Manager Purpose: Provide Regulatory and Quality Assurance support to the business. To operate as a member of the RA team with a mandate to promote a regulatory sound business practice and support the continuous improvement ethic throughout the organisation. Responsibilities: Reporting duties to RA ...
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Date: 18 April
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China,
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£40,000 - £70,000 per annum, negotiable, pro-rata, inc benefits
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7 applications
PRODUCT SPECIALIST - MEDICAL DEVICES - CHINA - NEGOTIABLE Job Title: EU Notified Body Medical Device Product Specialist China Primary Report: Technology Team Leader NB 0086 Secondary Report: Local manager (TBC) Location: Shanghai/Shenzhen, China Type: Permanent Employment Purpose of Position Conduct Technical Reviews for medical device CE conformity assessment certification ...
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Date: 6 May
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Singapore,
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SGD$250,000 - SGD$350,000 per annum
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4 applications
Organisation Description The client is a F&B manufacturer Job Description As a Regulatory Affairs Director for APAC regional your primary objectives will include, building and maintaining knowledge of national product registration processes and requirements to support business strategy and guide the product authorisation of existing and new products. You...
Organisation Description Job Description This position acts as the regional regulatory lead for assigned products and provides regulatory strategy and submission support to help drive the drug development process to bring innovative medicines to market. The job holder will be a key member of the regulatory sub-teams. The submission support could include the full spectrum, ...
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Date: 5 days ago
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Exeter, Devon
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£23,000 - £26,000 per annum
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9 applications
Job Description We have an exceptional opportunity to join this international firm within the marketing function. You will be working within the Marketing team, executing key brand projects and activities supporting the overall business strategies and objectives for the brand. You will also provide business insight in line with the business strategy and company budgets. The position is di...
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Date: 5 days ago
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Exeter, Devon
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£23,000 - £26,000 per annum
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8 applications
Job Description We have an exceptional opportunity to join this international firm within the marketing function. You will be working within the Marketing team, executing key brand projects and activities supporting the overall business strategies and objectives for the brand. You will also provide business insight in line with the business strategy and company budgets. The position is di...
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...
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Date: 3 days ago
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France,
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Salary not specified
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0 applications
Responsibilities: • Leading the submission process, including writing of documentation • Interaction with regulatory agencies • Defending of submissions • Prepare and maintain SAPs • Supervision of project analysis • Writing and reviewing of CRFs • Training and mentorship of other team members Requirements: • University qualification in statistics, mathematics or relevant subject area •...
Job Description My client is looking for an experienced individual to be involved in a range of activities from the global authoring of compliant SDS to delivering regulatory consultancy on behalf of a diverse client base, while also participating or leading in project management and customer contact activities. In this role: The Regulatory Affairs Consultant will be responsible for managi...
