Regulatory Affairs Manager

Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living.Regulatory Affairs plays a vital part in the process by ensuring our products are and remain compliant to the needs of the market and needs of patients.Our products are in 100 countries globally, and supporting this takes a huge effort.To do this, we're...

Regulatory affairs specialist required with a background in UK and EU REACHRegulatory Affairs Associate (Chemicals) Remote Salary - 35, ,000 PermanentMonday-Friday 9am-4.45pm with optional flexitime SRG is working with a closeknit materials manufacturer who make specialist adhesive and sealant products. This role is offering fully remote working to an...

Position Overview:A Compliance Specialist in Regulatory Affairs is sought after, possessing expertise in UK and EU REACH regulations.Role Type:Remote or hybrid working options available.Working Hours:Monday to Friday, 9 AM to 4 PM.Key Responsibilities:1. Develop and implement regulatory strategies to ensure adherence to compliance standards across the...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Indivior, a global specialty pharmaceutical company. As a key member of our R&D CMC team, you will be responsible for writing, reviewing, and approving Module 3 documentation, supporting the development and maintenance of new and existing dossiers for projects from...

Position Overview: The Lead Specialist in Regulatory Compliance plays a crucial role in guaranteeing adherence to medical device regulations across both national and international frameworks for various projects, products, and market introductions. Key Responsibilities: Oversee specific regulatory goals to align with the company’s Strategic Plan and...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Indivior, a global specialty pharmaceutical company. As a key member of our R&D CMC team, you will be responsible for writing, reviewing, and approving Module 3 documentation, supporting the development and maintenance of new and existing dossiers for projects from...

About the RoleWe are seeking an experienced CMC Dossier Writer to join our team at SRG. As a key member of our dossier team, you will be responsible for supporting the creation and maintenance of chemistry, manufacturing, and controls information in Module 3 dossiers.Key ResponsibilitiesSupport the development and maintenance of Module 3 dossiers, including...

About the RoleWe are seeking an experienced CMC Dossier Writer to join our team at SRG. As a key member of our dossier team, you will be responsible for supporting the creation and maintenance of chemistry, manufacturing, and controls information in Module 3 dossiers.Key ResponsibilitiesSupport the development and maintenance of Module 3 dossiers, including...

Position OverviewRegulatory Compliance SupervisorIndustry: Food ProductionSalary Range: £40,000 - £42,000Are you skilled in ensuring adherence to compliance and quality protocols with a passion for fostering ongoing enhancements to satisfy regulatory, organizational, and client expectations?This position is responsible for overseeing compliance through...

Position OverviewRegulatory Compliance SupervisorIndustry: Food ProductionSalary Range: £40,000 - £42,000Are you skilled in ensuring adherence to compliance and quality protocols with a drive for ongoing enhancement to fulfill regulatory, organizational, and client expectations?This position is responsible for overseeing compliance through systematic...

Job Title: Scientific Writer - Module 3 CMC DossiersType: 6 Month Contract - Potential for ExtensionSalary: Competitive and NegotiableLocation: Remote - Hybrid Working ArrangementSRG is working exclusively with a global specialty pharmaceutical company dedicated to transforming addiction into a recognized and treated chronic disease.We are seeking an...

Job Title: Scientific Writer - Module 3 CMC DossiersType: 6 Month Contract - Potential for ExtensionSalary: Competitive and NegotiableLocation: Remote - Hybrid Working ArrangementSRG is working exclusively with a global specialty pharmaceutical company dedicated to transforming addiction into a recognized and treated chronic disease.We are seeking an...

Job Title: CMC Dossier Development SpecialistJob Type: 6 Month Contract - Potential to ExtendSalary: Competitive and NegotiableLocation: Remote - Hybrid Working PossibleSRG is a global specialty pharmaceutical company dedicated to transforming addiction from a global human crisis to a recognized and treated chronic disease.We are seeking an analytical...

Job Title: CMC Dossier Development SpecialistJob Type: 6 Month Contract - Potential to ExtendSalary: Competitive and NegotiableLocation: Remote - Hybrid Working PossibleSRG is a global specialty pharmaceutical company dedicated to transforming addiction from a global human crisis to a recognized and treated chronic disease.We are seeking an analytical...

Job Title: Dossier Development Scientific WriterType: 6 Month Temporary Position - Potential for ExtensionSalary: Competitive and NegotiableLocation: Remote/Hybrid - Flexible Working ArrangementsSRG is a leading provider of specialized services to the pharmaceutical industry, dedicated to transforming addiction from a global human crisis to a recognized and...

Job Title: Dossier Development Scientific WriterType: 6 Month Temporary Position - Potential for ExtensionSalary: Competitive and NegotiableLocation: Remote/Hybrid - Flexible Working ArrangementsSRG is a leading provider of specialized services to the pharmaceutical industry, dedicated to transforming addiction from a global human crisis to a recognized and...

Regulatory Compliance LeadJoin a prominent player in the food production sector, catering to both major retail and food service clients.Key Responsibilities:Oversee adherence to quality management systems through systematic evaluations and inspections.Support the Technical Team in daily compliance operations, ensuring that standards align with external audit...

About the Role As a Quality Engineering Director, you will play a pivotal role in ensuring the highest standards of quality across our manufacturing and supplier networks. You'll lead a team of dedicated professionals, fostering a culture of continuous improvement and compliance within our Hull site. Key Responsibilities Provide strategic direction and...

Job DescriptionAre you a skilled analytical chemist looking to leverage your expertise in Module 3 Dossiers within a CMC environment? Do you have a passion for regulatory writing and a desire to drive business growth in a rapidly expanding company?Job Title: Dossier Development Scientific WriterType: 6 Month temporary contract with potential for...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Indivior, a global specialty pharmaceutical company. As a key member of our R&D CMC team, you will be responsible for writing, reviewing, and approving Module 3 documentation, supporting the development and maintenance of new and existing dossiers for projects from...