Regulatory Specialist

An opportunity for a Chemical Regulatory Affairs Specialist to join a global chemical trade association as manager of global regulatory intelligence. You will be responsible for: Regulatory horizon scanningTracking and analysing updates and changes to global chemical regulationsAssessing the impact on members substances Working with a range of stakeholders...

Global household name speciality chemical companyResponsibility for National and Regional regulatory compliance Diverse business units – complex aqueous mixtures and substancesBecome a regulatory subject matter expert This will be a highly diverse role; typical duties include answering complex customer regulatory enquiries, researching/impact assessing...

Regulatory Affairs Specialist - Fully RemoteThis is an excellent Regulatory Affairs Specialist / RA Specialist, working for a company with a growing reputation in their field. The successful Regulatory Affairs Specialist / RA Specialist will have hands-on knowledge of FDA regulations, ISO standards & SaMD - as well as proven experience working with medical...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to support pre- and post-market requirements, as well as the ability to...

As a Regulatory Publishing Specialist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.As a Regulatory Publishing Specialist you will be fully dedicated to a Top-5 pharmaceutical company. While working for our client, you will be able to profit from ICON through continued...

The business provides scientific, technical, and legislative support to the food and beverage industries worldwide. About the Regulatory Affairs Advisor jobThe purpose of your role will be to ensure provision of safe, honestly marketed food meets legal, commercial and moral standards. Key tasksMaintain and extend a high level of awareness of current food...

Job Title: Regulatory Affairs Specialist - Medical Device Location: Fully remoteCompany Description:We are a leading healthcare company dedicated to improving patient outcomes through innovative medical technologies.Our commitment to quality and compliance drives us to seek talented professionals to join our Regulatory Affairs team.Position Overview:As a...

Senior Regulatory Affairs Specialist - Medical Device Main Purpose of Job and Objectives:Perform Regulatory tasks to ensure compliance with regulations.Prepare regulatory documentation and submissions for product approvals.Develop regulatory plans/strategies for new products and changes to existing products.Participate in Design Control and Risk Management...

Looking for a new Regulatory Writing contract? Excited to announce that Barrington James are working with a Consultancy who are looking to grow their team. They are looking for an experienced Freelance Regulatory Writer, based in Europe! The details of the contract: Flexible FTE 12 month contract Remote Outside IR35 You will be responsible for: ...

Our Client, a UK Based Quant Hedge Fund, are looking for a regulatory reporting specialist to join their growing firm in a new Regulatory Reporting team on a permanent basis.Responsibilities:Assisting the team with day-to-day operations of regulatory reporting– Short Selling Disclosure, REMIT, EMIR, MAS, Transaction Reporting etcImprove reporting processes...

SENIOR MEDICAL WRITER (Germany, UK, USA, Canada, Portugal, Italy, Ireland)Only candidates who meet the following requirements will be considered:Candidate must live in one of the following countries: Germany, UK, USA, Canada, Portugal, Italy, Ireland. Applicants will work from one of our offices (Frankfurt, Germany; Cambridge, UK; Durham, NC, USA) or...

SENIOR MEDICAL WRITER (Germany, UK, USA, Canada, Portugal, Italy, Ireland)Only candidates who meet the following requirements will be considered:Candidate must live in one of the following countries: Germany, UK, USA, Canada, Portugal, Italy, Ireland. Applicants will work from one of our offices (Frankfurt, Germany; Cambridge, UK; Durham, NC, USA) or...

Compliance Specialist£80kA leading brand in the FS space, who specialise in supporting firms with advisory, risk management and capital requirements, are looking for a Compliance Specialist to tackle a broad role in Governance and Compliance.The roleDevelop the current compliance programme (policies and procedures)Complete audits and assessments from a risk...

Compliance Specialist£80kA leading brand in the FS space, who specialise in supporting firms with advisory, risk management and capital requirements, are looking for a Compliance Specialist to tackle a broad role in Governance and Compliance.The roleDevelop the current compliance programme (policies and procedures)Complete audits and assessments from a risk...

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of...

Seeking a Compensation Specialist to support on all compensation activity across the UK within a banking institution. It is a fantastic opportunity with a breadth of responsibilities for an individual to continue to grow and develop expertise in this space.Responsibilities Include:Providing expert advice relating to all aspects of compensation to HR Business...

Company: Generis Enterprise Technology LimitedJob Title: Training Documentation Specialist (Remote)Location: Remote – UKContract Status: Full-time / Permanent Staff - 40 hours per week Mon-FriSalary: Dependent on experienceTraining Documentation SpecialistOverview: The Training Documentation Specialist plays a critical role in creating and maintaining...

Company: Generis Enterprise Technology LimitedJob Title: Training Documentation Specialist (Remote)Location: Remote – UKContract Status: Full-time / Permanent Staff - 40 hours per week Mon-FriSalary: Dependent on experienceTraining Documentation SpecialistOverview: The Training Documentation Specialist plays a critical role in creating and maintaining...

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization),...

Company profile For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization),...