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Your next employer is at the forefront of developing advanced polymer systems for engineering maintenance. Industry has revolutionised the ways in which it solves repair and maintenance problems through the use of their Advanced Polymers and Repair Composites. Due to sustained and continued growth they are now looking for a Regulatory Officer to join their team Candidate Requirements - Essential - Ability...
Regulatory Officer £18,000 - £23,000 Harrogate Invigorate Recruitment are working with a client in the Harrogate area who are looking for a Regulatory Officer to join their busy team. The successful individual will provide essential support and assistance to the team, ensuring compliance with worldwide safety, health and environmental legislature which governs the manufacture and s...
Interested in a career in Food Legislation? 12 Month Maternity Cover Contract. Leatherhead Food Research is an independent, internationally recognised and trusted partner to the global food and drink industry. Our unique portfolio of products which includes regulatory advice, scientific consultancy and innovative research has attracted over 1500 companies worldwide. Our Members represent a who’s who of ...
  • Date: Yesterday
  • Croydon, Surrey
  • £35,000 - £50,000 per annum
  • 2 applications
Pharmaceutical Drugs Safety Scientist Contract - Croydon Opportunity : Are you currently working in drugs safety and pharmacovigilance? Are you looking for your next contract? Want to work for global leaders within pharmaceutical drug development? Yes then please read on. Your role as a Pharmaceutical Drugs Safety Scientistwill involve monitoring and managing the safety aspects of the companies portf...
  • Date: Yesterday
  • Croydon, Surrey
  • £35,000 - £50,000 per annum
  • 0 applications
Pharmaceutical Drugs Safety Scientist Contract - Croydon Opportunity : Are you currently working in drugs safety and pharmacovigilance? Are you looking for your next contract? Want to work for global leaders within pharmaceutical drug development? Yes then please read on. Your role as a Pharmaceutical Drugs Safety Scientistwill involve monitoring and managing the safety aspects of the companies port...
We are currently looking for a Pharmacovigilance Officer to join a leading Generics company based in London. KEY DUTIES AND RESPONSIBILITIES: The successful Pharmacovigilance Officer will be expected to: 1. Have knowledge and use of the Pharmacovigilance database for processing of Adverse Events and Adverse Drug Reactions. Conduct literature searches and obtain literature articles and reviews. Submit AEs and ADR...
We are currently looking for a Regulatory Affairs Officer to join a leading Generics company based in London. KEY DUTIES AND RESPONSIBILITIES: The successful Regulatory Officer will be expected to: 1. Ensure that the company's products comply with the regulations of the MHRA. In addition provide regulatory information, guidance and support to the R&D, Commercial, Clinical and Quality functions with respect ...
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...
This role would suit a Business/Pharmaceutical graduate Our client is looking for someone to work within their regulatory team dealing with administration and secretarial duties: Key skills required are: -Taking Minutes -Excellent IT skills - word, excel, adobe -Bookmarking in adobe, spreadsheets with formulas in excel, typing (speed and accuracy). -Editing documents. Previous experience withi...
Working with an international biopharmaceutical company with operations in Europe, North America, Australia and Japan; this company is an industry leader at an exciting time in their 30 year history. We are seeking a Senior Manager of Regulatory Affairs to join them on a permanent basis. Broad Function Provide leadership and advice on chemistry, manufacturing and controls (CMC) regulatory affairs and compl...

13 jobs matching this search were posted in the last week

Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
Laboratory Solutions are looking to recruit a UK Regulatory Affairs Manager(Established Pharma Division) for a Global Healthcare company based in Oxfordshire. A successful candidate will be able to manage the day-to-day activities of a regulatory team. Ensure the registration and regulatory compliance of UK/Ireland/Malta products with relevant national and European regulatory requirements. A high degree of technical competence ...
  • Date: 3 days ago
  • Switzerland,
  • Salary not specified
  • 0 applications
This is a new opportunity for an expert in Regulatory Early Development to lead early phase projects in a leading international pharmaceutical company in Switzerland. This position is to lead regulatory contact and expertise for assigned Therapeutic areas from Candidate Selection through to POC/DDP. In this role you will • Lead and coordinate all regulatory strategy for early development projects for assigned Disease ...
  • Date: 1 week ago
  • Llandysul, Dyfed
  • £75,000 - £85,000 per annum
  • 0 applications
Newly created, major role within this highly successful, International biopharmaceutical organisation ROLE Collate and review relevant data for submission to regulatory authorities Ensure that the company complies with all regulatory licenses and remains at a high level of legislative compliance on chemistry, manufacturing and controls through continual review of published information from relevant reg...
My client are a leading pharmaceutical company based in the East Midlands, they are currently looking for a Regulatory Affairs associate to join their well established team. The Role: You will be responsible for coordinating regulatory directives. You'll answer to governing bodies such as the MHRA on behalf of the company. You'll be responsible for both external and internal regulations in accord...
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Our client are an established GMP pharmaceutical company who are looking for an experienced Regulatory Officer for a long term contract. Your position in this role who be focussed on providing regulatory support to marketed products for a range of products across the EU including inhalation, transdermal and conventional dosage forms. Responsibilities include: • Completion of renewals and associated follow up • Completion ...
  • Date: 16 May
  • Italy,
  • Salary negotiable
  • 2 applications
My client is looking for a Senior Regulatory Affairs Group Manager to be based in Italy. Candidates with strong biologics and development experience would be very well suited to this position. This company is highly respected and you will be part of their international team. They will provide relocation assistance. The ideal person will have the following experience. • Up to 10 years pharmaceutical regulatory affairs e...
  • Date: 16 May
  • Italy,
  • Salary negotiable
  • 1 application
My client is looking for a Regulatory Affairs CMC Manager to be based in Italy. If you have a Biologics background they would be particularly keen to speak with you. This is an excellent global pharmaceutical company with huge potential career growth. They are developing exciting medicine and you will be able to work at an international level. RELOCATION COSTS AVAILABLE Do you have the following experience and intere...
An opportunity has arisen for recent Science Graduate with limited experience in regulatory affairs to developtheir career within a well-established company based in London. The successful candidate will be required to prepare and submit applications for new and existing licences, set up and maintain a complete, accurate and consistent database entry of records and submission activity.Keep up to date with changes in pr...
Superb, brand new opportunity for a competent Regulatory and Quality Affairs Manager to join this rapidly growing, global radiotherapy equipment developer. As an experienced Regulatory and Quality Affairs Manager you will assist in extending the company’s expansion into new markets and territories. The Company: Our highly successful North London based client is a fast growing 3D imaging medical technology company speci...
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