Offres regulatory affairs à CarshaltonCréer des alertes d'emploi

Supply Planner – UK (Pharmaceuticals) I’m partnering with a leading global pharmaceutical organisation to recruit a proactive Supply Planner for their UK operations team. This role ensures the smooth flow of products into the UK market, maintaining optimal inventory levels and strong service performance. (Approx. 10–20% travel.) Key Responsibilities • Coordinate product replenishment from global sites into UK logistics providers., • Maintain inventory levels across multiple locations, ensuring effective stock rotation., • Manage direct-to-pharmacy order fulfilment and resolve delivery issues., • Track service levels, analyse root causes, and drive corrective actions., • Report key supply chain KPIs and recommend process improvements. Key Requirements • 3+ years’ experience in supply chain planning (pharma, FMCG, or similar)., • Solid knowledge of inventory, replenishment, and fulfilment processes., • Strong Excel and ERP skills., • Excellent communication and problem-solving ability., • Collaborative team player., • Degree in Supply Chain, Engineering, Business, or related field., • Experience with SAP, PowerBI/Tableau, or automation tools., • Background in 3PL/distributor management., • Understanding of UK GDP regulations. About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth at Planet Pharma for more information: E:

Position: Patient Solutions Senior Associate - Cardiometabolic Health Location: Near Hook, UK - Hybrid Client: Pharmaceutical Main Responsibilities • Lead and manage the digital Patient Support Programme (PSP) for weight management from design to delivery., • Act as the primary contact between the company, the vendor, and internal teams (medical, compliance, IT, marketing)., • Oversee vendor performance and ensure full compliance with ABPI, MHRA, GDPR, pharmacovigilance, and NHS standards., • Manage content approval and certification through Veeva Vault PromoMats, maintaining audit trails and compliance documentation., • Coordinate cross-functional collaboration to ensure all materials align with strategic and regulatory objectives., • Plan and execute the PSP launch, ensuring all assets, training, and field materials are ready and compliant., • Deliver briefings, toolkits, FAQs, and activation playbooks to support internal teams and external communications., • Monitor programme performance, patient engagement, and service quality through data insights and reporting., • Gather feedback from patients, HCPs, and field teams to drive continuous improvement and optimise content., • Manage programme budget, resources, and scalability, ensuring strong value and measurable outcomes. Main Requirements • Degree-level education (or equivalent professional experience) in a relevant field., • Minimum 2 years’ experience in pharmaceuticals, healthcare, or patient support programmes (cardiometabolic experience preferred)., • Proven project management skills with experience delivering complex, cross-functional initiatives., • Strong knowledge of the ABPI Code of Practice and experience managing compliance for PSPs or similar programmes., • Proficiency with Veeva Vault PromoMats or similar systems., • Excellent communication, collaboration, and stakeholder management skills., • Ability to balance strategic goals with operational delivery and manage multiple priorities under tight timelines., • Strong analytical, problem-solving, and decision-making capabilities. ABOUT PLANET PHARMA Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

The Environment & Sustainability Risk and Compliance Leader will be responsible for environmental and sustainability compliance and risk management for the International Family Care & Professional (IFP). Risk Management, Legal, Research & Engineering, Regulatory Affairs, Government Relations and Com

Regulatory Affairs Consultant – EU Strategy.UK-based, Hybrid – 3x a week on-site in Surrey, UK.Represent a particular region for regulatory sciences (US, EU or EM).Provide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST).Lead and implement regional regulato

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

Job Title: Regulatory Affairs Training Manager Location: White City, London Contract: 18 months / Hybrid few days per month Hours: 40 hours per week Rates: £430 p/d Via Umbrella Company Job Description SRG are looking for RA training manager to join a global pharmaceutical company b

Your Background: Educated to degree level in a relevant life sciences field with experience in Regulatory Affairs. Experience in a Regulatory Affairs role in food, supplements, pharma or cosmetics and comfortable in learning other Regulations Flexibility to switch between product categories an

Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications.

Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. Strong CMC regulatory experience, including preparation and review of Module 3 CTD. Solid understanding of pharmaceutical manufacturing processe

The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group.

Are you passionate about quality, compliance, and making a real impact in the medical device industry? We're looking for a Quality Assurance and Regulatory Affairs Specialist to join our team and help ensure that our products meet the highest standards of safety and performance. Job Title: Qual

Regulatory Affairs Specialist (Full-time, Permanent). What does Regulatory Affairs Specialist mean at our client?. Provide in depth review of regulatory matters for food, feed supplements activity in the EU, UK and outside the EU entities for our client.

Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications.

Regulatory Affairs Specialist (Full-time, Permanent).

Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications.

What does Regulatory Affairs Specialist mean at our client Provide in depth review of regulatory matters for food, feed supplements activity in the EU, UK and outside the EU entities for our client. Regulatory Affairs Specialist (Full-time, Permanent) Unlock your potential with our client Our client

Ensure regulatory submissions are made on time and any delays are communicated to all relevant stakeholders in a timely manner so as to minimize impact to the business Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with

The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group. A RA Associate also updates and maintains regulatory activities in the Regulat

Regulatory Affairs Specialist (Full-time, Permanent).

All potential candidates should read through the following details of this job with care before making an application.Thanks for checking out our vacancy, we're delighted you want to learn more about Dechra!.Dechra are a growing, global specialist within the world of veterinary pharmaceuticals.Our e

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

The Opportunity The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group. A RA Associate also updates and maintains regulatory activiti

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).

A global e-commerce leader in London is seeking a motivated Legal Counsel to provide legal guidance on regulatory compliance and consumer product safety regulations. The ideal candidate will support various teams, manage risks, and navigate the changing regulatory landscape.

A leading pharmaceutical company is seeking a Head of External Partnerships to oversee global strategic partnerships within Regulatory Affairs. The ideal candidate should have significant experience in Regulatory Affairs and vendor management, along with exemplary negotiation and leadership skills.

As a Regulatory Affairs and Quality Assurance (RAQA) Manager, you will utilise your extensive technical expertise to ensure that the company complies with regulatory requirements in all applicable global regions and supports the company to meet the required quality standards and objectives in all bu

The Regulatory Affairs (RA) Associate in the Global RA Coordination team is responsible for managing the Global RA inbox, coding invoices, reporting sales figures, archiving, and providing general support to the RA group. A RA Associate also updates and maintains regulatory activities in the Regulat

Regulatory Affairs: Support engagement with regulatory authorities, including the UK’s Office for Product Safety and Standards (OPSS) and EU market surveillance authorities. Legal Counsel - Regulatory and Government Affairs. Legal Counsel - Regulatory and Government Affairs.

We are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio‑Metabolic to join our Global Regulatory Affairs team. Global Regulatory Affairs Associate Director (Cardio-Metabolic). Global Regulatory Affairs Associate Director (Cardio-Metabolic).

Regulatory Affairs Senior Manager - UK Pharma Leader (Permanent Role)Location: London, UK | Sector: Pharmaceuticals | Salary: Competitive + Benefits Are you a seasoned Regulatory Affairs professional looking for a strategic role where your expertise directly impacts patient access to life-changing m

Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Drive global Regulatory Affairs strategies for the portfolio, including managing internal and external stakeholders. Global Associate Director, Regulatory Affairs.

Contributing regulatory guidance in order to enhance product development - Ensuring that product development is aligned with the company’s strategy business model as well as global regulatory requirements - Acting as a point of contact between the company and regulatory agencies whilst pertaining

The WEP Clinical Senior Regulatory Affairs Manager plays a critical role in shaping and delivering regulatory strategies across a diverse portfolio of projects, including Post‑Approval Named Patient Programmes, Expanded Access Programmes, Compassionate Use Programmes, and Clinical Trials. Lead, me

Track and ensure regulatory compliance obligations such as reporting requirements into regulators are met in a timely manner, and support teams on the development, maintenance, and documentation of regulatory reporting requirements. Assistant Counsel or Specialist, Government, Policy and Regulatory

This remote position requires 3–5+ years of experience in regulatory affairs and a Bachelor's degree. A leading life sciences firm is seeking a Director, RIMS Strategy Consultant to oversee regulatory operations and manage client solutions.

A leading biotechnology company is looking for a Director Global Regulatory Affairs - CMC to lead regulatory affairs for investigational medicinal products. Required qualifications include over 9 years of experience in Regulatory Affairs CMC and a relevant degree in pharmacy or equivalent. The succe

The Regulatory Affairs team are the owners of PIC’s regulatory strategy including being responsible for managing the relationships with the relevant UK regulators (PRA and FCA). To work with the Head of Regulatory Affairs to provide papers to Management, Board Risk Committee, Audit Committee and B

Responsible for the provision of full regulatory input and support for assigned products across the submission and assessment phase which includes the preparation, submission and response to questions for new Marketing Authorisation Applications.

Minimum of 5 years governmental affairs / regulatory affairs / legal experience ideally within the financial services or crypto‑asset industry in the UK. The successful candidate is someone with an understanding of the regulatory environment pertaining to the crypto‑asset industry / stablecoin i

The Regulatory Affairs team are the owners of PIC’s regulatory strategy including being responsible for managing the relationships with the relevant UK regulators (PRA and FCA). To work with the Head of Regulatory Affairs to provide papers to Management, Board Risk Committee, Audit Committee and B

Act as global regulatory affairs CMC lead for the assigned development and/or commercial products and/or projects and define and execute the Global Regulatory CMC strategy from pre‑clinical stage up to Marketing Authorisation and/or lifecycle maintenance. More than 9 years professional working exp

In depth knowledge of UK and European regulatory affairs legislation and guidance. Provide regulatory input on pharmaceutical development and CMC and review quality documentation to ensure regulatory compliance with UK and EU legislation. Substantial regulatory experience across the full product lif

To work with the Head of Regulatory Affairs to provide papers to Management, Board Risk Committee, Audit Committee and Board meetings, ensuring they are kept informed of regulatory issues, projects, forward looking activities and relationship. The Regulatory Affairs team are the owners of PIC's regu

Working within the Quality Assurance and Regulatory Affairs team, the Senior Regulatory Affairs Engineer assures regulatory requirements are met for new product introduction and design changes to established products. It contributes to providing regulatory solutions to business requirements and chan

Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Knowledge of regulatory frameworks and external environments as it applies to project specific global regulatory strategy document (GRSD) delivery. Global Associate Director, Regulatory Aff

Crucial to your success will be your ability to work closely with the FDA and other regulatory bodies to agree innovative scientific approaches and provide the internal leadership to convert this into a regulatory strategy to be followed and implemented. Vice President Scientific Affairs and Regulat

A leading pharmaceutical company in the United Kingdom is seeking a Mid-Senior level Regulatory Affairs Specialist to provide regulatory input and support for new Marketing Authorisation Applications. The ideal candidate will have a strong background in regulatory submissions and CMC, with an emphas

We are seeking an experienced Regulatory Affairs professional specializing on in vitro diagnostics (IVD) and Companion Diagnostics (CDx) to join our Global Regulatory Affairs team. Minimum 5+ years of experience in Medical Device/IVD regulatory affairs. Demonstrated experience with in vitro diagnost