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As a Registered Nurse at a Barchester care home, you'll look after the physical, psychological, and social needs of our residents to help us deliver the quality care they deserve. You'll have the autonomy to do things the right way and be truly valued and respected for what you do. We'll look t...

Axis has experienced continual growth since its establishment in 1986, we’re not aiming to be the biggest service provider, however we intend to be the best. We work with some of the UK’s largest building owners, landlords & facility managers to provide strategic building repairs, planned mainte...

Multi Skilled Maintenance Engineer 42 hours per week (2 Days, 2 Nights, 4 Off) Sittingbourne (ME10 3NB) £53,768 + benefits Marshalls is the UK's leading hard landscaping manufacturer and has been supplying superior natural stone and innovative concrete products to the construction, home improve...

DOCUMENT CONTROLLER Our client, a well established and reputable construction company who specialise in mechanical & electrical commercial & residential construction projects is currently looking for a document controller to join the team based in Sittingbourne. This is a full time, office base...

Health & Safety Advisor – COOK Location: Based in Sittingbourne with some travel to other sites. Salary: £35,000 - £40,000 Hours: Mon–Fri 8:30am–5pm (flexibility required) Purpose: At COOK, we embrace a ‘culture of care’ in our work environment, ensuring safety and well-being for our staff....

Social network you want to login/join with: col-narrow-left Busy Bees Nurseries Sittingbourne Other - Yes col-narrow-right 7e84d7f9e9e7 4 02.06.2025 17.07.2025 col-wide Job Summary Are you passionate about early childhood development and ready to take on a leadership role? Sittingb...

Join to apply for the Senior Associate Process Development Engineer role at Jazz Pharmaceuticals 4 days ago Be among the first 25 applicants Join to apply for the Senior Associate Process Development Engineer role at Jazz Pharmaceuticals If you are a current Jazz employee please apply via the...

Alpha Scientific is at the forefront of chemical and microbiological testing, reliably providing organisations with detailed analysis of water and air quality. We are a team of highly skilled and trained scientists who work from purpose-built, UKAS accredited laboratories in Sittingbourne, Slou...

ABOUT THE ROLE As a Registered Nurse at a Barchester care home, you'll look after the physical, psychological and social needs of our residents to help us deliver the quality care they deserve. We'll look to you to create a safe and supportive environment for residents with range of physical an...

ABOUT THE ROLE As a Registered Nurse at a Barchester care home, you'll look after the physical, psychological and social needs of our residents to help us deliver the quality care they deserve. We'll look to you to create a safe and supportive environment for residents with range of physical an...

DOCUMENT CONTROLLER Our client, a well established and reputable construction company who specialise in mechanical & electrical commercial & residential construction projects is currently looking for a document controller to join the team based in Sittingbourne. This is a full time, office bas...

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. - The Senior support worker will work closely with the Team Leader and Manager in the running of the homes and in supporting other team members. You will be responsible for newly referred YPs and ...

A new and exciting opportunity has arisen for a CNC Miller/Setter to join a UK known Precision Engineering Company in the Sittingbourne area! With no day ever being the same, the CNC Miller/Setter role offers the opportunity to support the aerospace and motorsport industries through CNC Machining...

About the Client: Our client specialises in the construction and upgrade of overhead and underground electricity networks that power homes and businesses. With a strong reputation for quality and reliability, they’ve recently secured a major tender with a Distribution Network Operator (DNO) and a...

This role requires you to be onsite full time based at our site on Kent Science Park in Sittingbourne. Brief Description: The Associate Director, R&D – Process Chemistry heads the process research and development team within the Discovery and Medicinal Chemistry group at Kent Science Park, adopti...

Social network you want to login/join with: Job Title: General Manager As the General Manager, you will oversee the seamless delivery of all racing and non-racing events, ensuring every aspect runs efficiently, safely, and with the welfare of all greyhounds as a top priority. Your leadership will...

Role Description Join Our Team as a PBS Registered Manager Location: Maidstone, Sittingbourne & Herne Bay, Kent Salary:£47,150 per annum plus benefits. Hours:37.5 hours per week, on-call rota, additional hours to meet service requirements. Contract:Full-time, permanent Driving Requirement:A valid...

This is a fantastic opportunity for someone with a strong background in regulatory documentation—particularly SmPCs, PILs, and labelling compliance—to join a high-performing regulatory affairs team. Collaborate with internal teams including Regulatory Affairs, Medical, Pharmacovigilance, and Art

The Role: Senior Regulatory Writer. You’ll play a key role in writing and reviewing a broad range of regulatory documents, with a particular focus on strategic, high-level submissions for global health authorities. Develop and deliver high-quality regulatory documents in line with guidelines.

As a Tier 1 ranked firm in the Legal 500, the firm is continuing to expand and is looking to appoint a 1+ PQE Crime and Regulatory Solicitor to support the team in handling complex regulatory cases, motor crime, and inquest work. Crime & Regulatory Solicitor – Manchester / Birmingham – Up to £6

Proven experience as a lead author on multiple regulatory documents, including at least 3 of the following: protocols, clinical study reports, clinical summaries, clinical overviews, investigator brochures, narratives, briefing documents, or regulatory response documents. Regulatory Writing, Brie...

They are strengthening the team by hiring a Regulatory EU Lead, to be based in their offices in West London, hybrid working set-up.

We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Our work spans a wide range of high-quality clinical and regulatory documents, including:. Regulatory responses to health authorities.

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Senior Regulatory Medical Writer. This is a unique opportunity to join a high-performing regulatory writing team, with exposure to inte...

Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical commu...

Job Title: Regulation 44 Visitor.Remote-based with regional travel.We are currently recruiting for a committed and experienced.

Reporting into our Head of Regulatory, Technical & Quality, you will spearhead the regulatory compliance team, managing the Regulatory & Technical compliance for all retail partners and the business's innovative range of cosmetic products. As a Regulatory Manager, you will join the Regulatory Com...

Healthcare Regulatory Solicitor/Associate/Senior Associate - Top Tier Firm – Hybrid/Remote working. Healthcare Regulatory team with additional Solicitors to join at various different levels. Qualified Solicitors in regulatory/health/social care/education law, join from Solicitor level up to Senio...

The Regulatory Labelling and Artwork Specialist role is part of a project with a leading biopharmaceutical company focused on developing innovative treatments for rare and ultra-rare genetic diseases.

As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. Minimum of 5 years' regulatory writing experience in a medical communications agency or pharma/biotech setting. Strong understanding of...

Assisting with the preparation and submission of regulatory documents to regulatory agencies Maintaining product regulatory files Supporting Vigilance and Post-Market Surveillance activities Supporting the RA Manager with Regulatory review of new product technical file documentation What can we o...

The Department Leader for Regulatory Affairs is also responsible for acting as an active participant in team meetings that relate to changes to developed products that will require further registration and regulatory submissions. Compile product information for the preparation of technical files ...

CTD clinical summaries, investigator brochures) across multiple therapeutic areas Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations Review and quality-check clinical documentation, data outputs, and other supporting materials Liaise ...

We’re Hiring: Team Leader – Regulatory Affairs (IVD). A growing diagnostics innovator is building out its UK-based Regulatory Affairs team and looking for a. You’ll lead a small team (including RA officers and admin staff), take ownership of regulatory input into product changes and compliance

Additionally, you will assist in implementing a Regulatory Information Management system to track regulatory activities effectively. Partner with commercial and medical teams, and external regulatory partners. Contribute to new regulatory guidance preparation and communicate impacts.

Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations. Conduct background research to confirm references and stay aligned with current regulatory requirements. Previous experience producing regulatory documentation within a medical commu...

Smartedge’s Client is looking for an individual to help with their EU Labelling Strategist/ Labelling Manager (Regulatory Affairs) @ UK (100% Remote Work) Experince Required : Create, prepare, and revise CCDS, US and EU labeling for mature and life cycle products assigned to obtain company and/or...

We focus on recruitment in Regulatory Affairs, Registrations, REACH, CLP, SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors. ED, biology, evaluation, ecotoxicology...

Healthcare Regulatory Solicitor/Associate/Senior Associate - Top Tier Firm – Hybrid/Remote working. I am currently working with a standout Top Tier law firm that’s seen 11 consecutive years of growth — they are now looking to expand their Healthcare Regulatory team with additional Solicitors t

We are working with a leading international law firm to hire a Regulatory Lawyer to join their dynamic risk and compliance team in London. In this role you’ll provide expert guidance on a range of regulatory and professional risk matters, supporting senior leadership in maintaining the firm’s hi

About the Role: As a Senior Regulatory Medical Writer, you will independently lead the development of a wide range of core regulatory documents across various therapeutic areas. We’re currently collaborating with a global, award-winning medical communications agency to support their search for an...

Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. An experienced regulatory technologist with a minimum of 3 years in a cosmetic’s regulatory affairs. The regulatory team are focused on both regulatory compliance and customer ne...

Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. The regulatory team are focused on both regulatory compliance and customer need to ensure products meet the highest standards of quality and commerciality. Essential requirements...

You’ll be the lead advisor on all regulatory matters, managing a team of 3 people, and working closely with the Executive team and Board to ensure the business operates in full compliance with statutory and regulatory obligations, including those from the FCA and Gambling Commission. Regulatory C...

CTD clinical summaries, investigator brochures) across multiple therapeutic areas Ensure all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations Review and quality-check clinical documentation, data outputs, and other supporting materials Liaise ...

A minimum of 5+ years’ experience as a Regulatory Manager, Regulatory Team Leader, Regulatory & Compliance Manager, Regulatory Affairs Manager in the Cosmetics/Skincare/Haircare/Fragrance/Personal Care sector. If you are looking for a new role, get in touch today if you are an experienced Regulat...

Key Responsibilities Write, edit, and review regulatory documents in accordance with guidelines and client requirements Analyze and interpret scientific data to develop coherent and compliant narratives Collaborate with internal teams and clients to ensure high-quality, timely deliverables Manage...

Senior Vice President / Vice President of Regulatory Affairs. This executive role will lead global regulatory strategy, with a particular focus on the UK and EU, supporting the development of advanced genetic therapies using ASO technologies. Lead regulatory strategy and submissions across the UK...