Regulatory affairs jobs in HinckleyCreate job alerts

An experienced regulatory technologist with a minimum of 1 year in a cosmetics regulatory affairs. Managing an effective global regulatory horizon scanning process to ensure our regulatory processes remain future-fit. The regulatory team is focused on both regulatory compliance and customer needs to

Manage external regulatory service providers to align with business objectives and support the development and maintenance of an effective regulatory affairs function. Senior Manager Global Regulatory Affairs - Requirements:. Act as a subject matter expert on global regulatory requirements, includin

Senior Manager // Regulatory Affairs // Strategy // Leadership // Global // Oncology // Rare Disease // Life Cycle Management // Post Market // Development // FDA // EMA // ICH. As a Senior Regulatory Affairs Manager, you will:. A Senior Regulatory Affairs Manager will bring:.

As an Senior Manager, Global Regulatory Affairs, Precision Medicine, you will help develop and execute Precision Medicine regulatory strategy in alignment with the drug global regulatory strategy and in compliance with the appropriate IVD regulations. Represent Regulatory Affairs Precision Medicine

This position assists in maintaining organization’s Regulatory Affairs operational functions and direct lines of communication for, interactions with, and access to Regulatory Authorities/Agencies in the US and abroad, in compliance with regulatory guidance, regulation and laws. The Senior Manager

Philosophy that Regulatory Affairs is value-adding, not a bureaucratic function. It includes harmonising regulatory efforts for EU products of the UK portfolio, with MAH under UK portfolio while regulatory oversight remains with UK team post-Brexit. Specialise in managing regulatory affairs for EU p

We are looking to expand our Regulatory Affairs team and are currently looking for an experienced Regulatory Consultant to join us on a one-year fixed contract or a permanent basis. We are a forward-thinking regulatory affairs consultancy, DLRC Ltd takes the time to understand individual needs and f

Ensures effective collaboration with Global Regulatory Affairs CMC Strategists, Global Manufacturing and Global Quality SMEs for timely preparation and review of regulatory submission documentation. Maintains regulatory CMC dossier templates in alignment with current ICH and regional regulatory requ

This role involves leading the creation, development, and implementation of global/regional regulatory affairs procedures, ensuring compliance with regulatory requirements, and maintaining regulatory compliance status. Provide input to Regulatory Affairs Impact Documents (RAIDS). Lead the creation a

Develop and execute CMC-regulatory strategies and oversee the preparation of key regulatory documents, including Module 3 sections. Proven track record in CMC-regulatory affairs within the pharmaceutical industry. Lead and manage CMC-regulatory activities across various development and marketed prod

Ensures effective collaboration with Global Regulatory Affairs CMC Strategists, Global Manufacturing and Global Quality SMEs for timely preparation and review of regulatory submission documentation. Maintains regulatory CMC dossier templates in alignment with current ICH and regional regulatory requ

Lead a team of Regulatory Affairs Professionals responsible for the development, authorship, and maintenance of global regulatory submissions (e. Clinical Affairs, Business Development, QA, R&D, Program Management) to define and execute regulatory strategies for Leica Biosystems technologies in canc

Head of Regulatory Affairs - MedTech. A growing MedTech company is seeking an experienced Regulatory Affairs Leader. Strong industry experience operating in a Lead level role within Regulatory Affairs.

Lead a team of Regulatory Affairs Professionals responsible for the development, authorship, and maintenance of global regulatory submissions (e. Clinical Affairs, Business Development, QA, R&D, Program Management) to define and execute regulatory strategies for Leica Biosystems technologies in canc

This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical through clinical development for our programs. Associate Director / Director, Regulatory Affairs (EU- or UK-based). Responsible for regulatory clinical

This role will provide strategic regulatory and scientific support on non-clinical and clinical development plans and work with both Regulatory Affairs - Strategic Project Leads and Regulatory Affairs - Life cycle management teams with an objective of getting fast access of innovative medicines to p

The Senior Manager will interact closely with corresponding functional team members within the Company and will report directly to the Senior Director (EU Regulatory Lead), Regulatory Affairs. The Regulatory Affairs Senior Manager provides regional (EU and other ex-US countries) support for all regu

Proven track record in CMC-regulatory affairs within the pharmaceutical industry. Lead and manage CMC-regulatory activities across various development and marketed products, ensuring compliance and regulatory risk mitigation. Develop and execute CMC-regulatory strategies and oversee the preparation

Regulatory Affairs Consultant - Cosmetics. Regulatory Affairs Consultant - Cosmetics. Perform tasks associated with the Regulatory Affairs department at the highest level.

Work with the Global Regulatory Lead and Regulatory Affairs management to lead and define regulatory strategy and to compile and submit, in a timely manner, regulatory documents according to regulatory requirements and lead EU HA interactions. The Senior Manager of Regulatory Affairs Strategy, will

Job Overview: We are seeking an experienced Regulatory Affairs Consultant to support Clients France Regulatory Affairs (RA) team. ClinChoice is searching for a Regulatory Affairs Consultant – Cosmetics/Commodities for 12 months Contract with possibility of extension to join one of our consumer pro

Ensures effective collaboration with Global Regulatory Affairs CMC Strategists, Global Manufacturing and Global Quality SMEs for timely preparation and review of regulatory submission documentation. As a Senior Regulatory Affairs Specialist (CMC) you will be joining the world’s largest & most comp

Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinical Trial Applications (CTAs) and Marketing Authorization Applications (MAAs). Proven experience in CMC re

This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical through clinical development for our programs. Responsible for regulatory clinical trial applications, annual reports, IND and IMPD amendments, and mee

You will work with the Director of Policy and Regulatory Affairs (and colleagues in the policy team) to: (a) provide access for AFB members to Government, policy makers and regulators; (b) aggregate and represent members’ views and opinions to help shape and influence the UK political and regulato

This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical through clinical development for our programs. Responsible for regulatory clinical trial applications, annual reports, IND and IMPD amendments, and mee

Ensures effective collaboration with Global Regulatory Affairs CMC Strategists, Global Manufacturing and Global Quality SMEs for timely preparation and review of regulatory submission documentation. Senior Regulatory Affairs Specialist (CMC author) - Homebased in UK, Poland, Spain or Germany. As a S

Lead a team of Regulatory Affairs Professionals responsible for the development, authorship, and maintenance of global regulatory submissions (e. Clinical Affairs, Business Development, QA, R&D, Program Management) to define and execute regulatory strategies for Leica Biosystems technologies in canc

This position will contribute to the build-out of the regulatory affairs function at Edgewise and will provide regulatory expertise from preclinical through clinical development for our programs. Responsible for regulatory clinical trial applications, annual reports, IND and IMPD amendments, and mee

The Director of Regulatory Affairs will lead the regulatory function and play a central role in shaping and executing global regulatory strategies for our ophthalmology assets. Regulatory Affairs, with significant exposure to ophthalmology or related therapeutic areas. Strong experience in authoring

This role reports to the Senior Director, Regulatory Affairs and is part of the Global Regulatory Affairs Team located in Newcastle, UK and will be an on-site role. Lead a team of Regulatory Affairs Professionals responsible for the development, authorship, and maintenance of global regulatory submi

Ensures effective collaboration with Global Regulatory Affairs CMC Strategists, Global Manufacturing and Global Quality SMEs for timely preparation and review of regulatory submission documentation. Maintains regulatory CMC dossier templates in alignment with current ICH and regional regulatory requ

Proven experience in CMC regulatory affairs, with additional exposure to R&D, Manufacturing, QA, or QC. Planet Pharma is seeking a highly skilled regulatory affairs candidate with strong Chemistry, Manufacturing, and Controls (CMC) experience, particularly in preparing documentation for both Clinica

Be all you can be with Hamberley.At Hamberley, we believe that our residents deserve something ‘Extra Special, Every Day’.We're seeking a Kitchen Assistant to help us achieve our goals.As our kitchen assistant, you will play a vital role in supporting the day-to-day operations of our care homes

As a Cleaner for Tenpin, you will be responsible for ensuring our Customers have an.When it comes to keeping your site spick and span, we will need you to bring your 'A' game.We love to entertain! It's in our DNA!.We have lots more to offer from Houdini's Escape Rooms, to Karaoke rooms, 4D Laser Are

Cleaner - Dublin.Compass Group Ireland, contracted to.If you're a committed Cleaner looking for a role you'll shine in, we've got the position for you.Your key responsibilities will include:.Working alongside our cleaning and facilities teams to keep environments safe and hygien

RightTime Care are seeking Compassionate and Experienced Complex Care HCA's and Support Workers to provide high-quality, person-centred care to individuals with complex needs, including mental health conditions, learning disabilities, autism, acquired brain injuries, and challenging behaviours.You w

Due to growth within the business, a leading UK Pension Consultancy are now looking for a Pension Team Leader to join their firm.The ideal candidate will have a strong understanding around Defined Benefit scheme administration, alongside Team Management experience.Responsibilities for the role Inclu

It’s a role that will see you work closely with the senior leadership team and influence how regulatory compliance is embedded across the business.

Plymouth Customer Service Centre .At Currys we’re united by one passion: to help everyone enjoy amazing technology.As the UK’s best-known retailer of tech, we’re proud of the service our customers receive – and it’s all down to our team of 25,000 caring and committed colleagues.So you’l

We are looking to recruit Senior Regulatory Writers with at least 3 years' experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. We provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range of

Love being on the move and interacting with people from all walks of life? Proud to deliver quality goods on time and put a smile on thousands of faces every week?.Join Ocado Logistics where there are bags of possibilities.It's our mission to provide an outstanding customer experience.Whilst others

Your role will involve not just leading but also inspiring the sector and colleagues-ensuring that we continue to meet and exceed the standards outlined in the statutory and regulatory guidance's and standards.

We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas. Ensuring adherence to industry guidelines and regulatory standards.

Senior Medical Writer – Publications | Oxford (Hybrid).Looking for your next MedComms challenge? Join an independent, forward-thinking agency where you’ll deliver innovative publications in metabolic disease, mentor juniors, and enjoy the flexibility of hybrid working (1–2 days in Oxford).This

We are looking for an experienced Private Cleaner in Knutsford (24-30 hours per week).The Successful person will have a host of domestic cleaning experience and worked with high profile clientele in previous roles.The role will undertake day-to-day cleaning tasks around a large residential property.

You will act as a key member of the team, providing support to global offices on all aspects of risk, regulatory compliance, and conflicts. Assisting in on-boarding new clients and matters and ensuring that all details are correct in accordance with regulatory standards and firm policy. Reviewing an

Experience in the global regulatory environment, including familiarity with key regulatory bodies and essential regulatory documents. Reporting to the Director of Medical and Scientific Communications and working closely with Clinical Science, Clinical Operations, and Regulatory Affairs, this is a k