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Date: 1 week ago
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Reigate, Surrey
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£25,000 - £30,000 per annum
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6 applications
About Us From Huggies® diapers to Kleenex® facial tissues, Kimberly-Clark makes the essentials for a better life. Our 57,000 global employees are changing the world for the better with innovative products that create new categories and push existing ones to a higher level. While building our business, we’re also building careers through first-class education, engaging experiences and exposure to some of the world’s m...
Our client is an API and intermediate manufacturer based in Hertfordshire. They are currently looking for a Regulatory Affairs Officer to join their regulatory department. Responsibilities: - You will assist in the compilation, assembly and submission of Drug Master Files and Certificate of Suitability for our clients existing and new Active Pharmaceutical Ingredients. - To assist in...
Job Description: Our client is a growing CRO who are seeking an experienced senior regulatory specialist to co-ordinate their clinical trial and marketing authorisations and develop regulatory packages for each of their international submissions and sites. Candidate Requirements: The successful applicant will have extensive experience in a similar role, a medical/science background and excellent knowledge of the regula...
Quality Specialist, Edinburgh, £DOE This is a fantastic opportunity for an experienced Quality Specialist to join a well-established bio-manufacturing organisation, with an internationally recognised product portfolio. The main responsibilities of this role will include: -Complaint management -Root cause analysis of complex problems -Process improvements -Trend quality data from key data s...
An experienced Clinical Research Specialist required to join a large organisation. You will provide support to new product development projects in Skin & Wound Care and Infection Prevention Divisions. Preferably, you will have previous experience in independently leading clinical research programmes in medical devices or pharmaceuticals and a thorough understanding of clinical study. Educated to a high level within a related science field, ...
A specialist Recruitment firm based in Essex now offer a new career opportunity for a driven Senior or Principal Recruitment Consultant to manage a busy perm desk with the life sciences sector. This rapidly expanding firm work to an incredibly high standard with several high profile figures driving the firm at board level. Joining this team will see you take responsibility for developing a specialist area such as Medical Devices, Clin...
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Date: 7 June
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Taunton, Somerset
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£18,000 - £22,000 per annum, negotiable
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8 applications
Job Description My client, a manufacturer of specialist healthcare products, is recruiting for a Specifications Technologist for the team. Reporting to the Director of Quality and Regulatory Affairs, you will be responsible for risk assessment, approval and monitoring of all raw materials and suppliers. Principal Responsibilities: • Responsible for risk assessing, approving...
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Date: 7 June
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Taunton, Somerset
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£18,000 - £22,000 per annum, negotiable
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3 applications
Job Description My client, a manufacturer of specialist healthcare products, is recruiting for a Specifications Technologist for the team. Reporting to the Director of Quality and Regulatory Affairs, you will be responsible for risk assessment, approval and monitoring of all raw materials and suppliers. Principal Responsibilities: • Responsible for risk assessing, approving...
Regulatory Compliance Officer, North Yorkshire, Neg Salary + Bens An opportunity to join the regulatory affairs team at a successful and fast expanding specialist global chemical company. The regulatory affairs team is responsible for ensuring the compliance of the company’s products and to provide high quality regulatory support to the business. The role will involve proactively monitorin...
Chemicals Regulatory Affairs Officer, Harrogate, Neg Salary + Bens An opportunity to join the regulatory affairs team at a successful and fast expanding specialist global chemical company. The regulatory affairs team is responsible for ensuring the compliance of the company’s products and to provide high quality regulatory support to the business. The role will involve proactively monitori...
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...
Regulatory Affairs Manager - PPP, Cheshire, Excellent package + Bens An excellent opportunity to join a leading Global Crop / Plant Protection Product company and take responsibility for specific molecules at EU level . This will involve ensuring your molecules are included on Annex I or on the list of approved active substances, liaising with rapporteur Member States, identifying ...
Regulatory Affairs Manager - PPP, Cheshire, Excellent package + Bens An excellent opportunity to join a leading Global Crop / Plant Protection Product company and take responsibility for specific molecules at EU level . This will involve ensuring your molecules are included on Annex I or on the list of approved active substances, liaising with rapporteur Member States, identifying ...
14 jobs matching this search were posted in the last week
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Date: 31 May
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China,
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£40,000 - £70,000 per annum, negotiable, pro-rata, inc benefits
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13 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 ...
Our Client is looking for a RAQA Senior Specialist to Manage the Post Market Surveillance activities for UK division and provide support for other Countries in Europe where required. You will need to Provide maturity and significant RAQA experience and expertise to the UK and European RAQA Team including guidance on European Regulations /Policies and driving the Company’s Quality First Policy towards a state of the art Quality Manag...
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Date: 6 days ago
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Switzerland,
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Salary negotiable
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2 applications
Role: Regulatory Affairs Specialist (Jnr) Location: Bern, Switzerland Rate: Negotiable Job Type: Contract POSITION SUMMARY: This position is responsible for executing the electronic publishing of regulatory submissions for coun...
Organisation Description I am currently recruiting for a global manufacturing company for an Indirect buyer Job Description The key responsibilities of this role include the management of Indirect Material spend across a number of commodities including amongst others, travel, facilities, and software licensing. Other key responsibilities will include the development and executio...
Organisation Description I am currently recruiting for a global manufacturing company for an Indirect buyer Job Description The key responsibilities of this role include the management of Indirect Material spend across a number of commodities including amongst others, travel, facilities, and software licensing. Other key responsibilities will include the development and executio...
Organisation Description My client is an API and intermediate manufacturer based in Hertfordshire. They are currently looking for a Regulatory Affairs Officer to join their regulatory department. Job Description - You will assist in the compilation, assembly and submission of Drug Master Files and Certificate of Suitability for our clients existing and new Active Phar...
Organisation Description The primary repsonsibilities of this position is to manage the life-cycle of marketed products in the companies therapeutic group along with supporting development activities on projects in development. Job Description Scope and Responsibilities: Accountabilities - Executes work procedures that are tactical in nature ...
Pharmaceutical Senior Compliance Manager - Croydon Opportunity : This is a great opportunity for someone who has good pharmaceutical quality assurance and regulatory affairs compliance experience to join a growing pharmaceutical manufacturing company in Croydon. Your role as a Senior Compliance Manager will involve leading and managing quality assurance, regulatory affairs and compliance projects. Th...
Pharmaceutical Head of Quality Management and Compliance - Croydon Opportunity : If you are looking for a new exciting opportunity or your next career change then this is a one off opportunity you do not want to miss out on. Your role as Head of Quality Management and Compliancebased in Croydon will involve leading and managing the quality and regulatory affairs departmentto achieve corporate complian...
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Date: 11 June
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Singapore,
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Salary negotiable
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0 applications
Organisation Description This MNC is one of the world’s leading FMCG companies with their regional headquarters in Singapore. They are seeking a qualified, highly motivated and dynamic individual to lead the Regional Regulatory Affairs team. Job Description • Managing Regulatory Affairs for all products for the region, reporting to a Regional RA Director based in the APAC region....
Organisation Description Reed Scientific are currently recruiting for a Quality and Regulatory Manager for their client who are an Oxfordshire based Life Science organisation. This position is responsible for the day to day management of the Quality Management System and of effective quality assurance and quality control of the company’s products and processes. You will also manage the reg...
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...
