Regulatory affairs jobs in ChorleyCreate job alerts

A Senior Regulatory Affairs Manager will bring:. Regulatory Affairs experience in the pharmaceutical or biotech industry, with proven success in leading global submissions. Senior Manager // Regulatory Affairs // Strategy // Leadership // Global // Oncology // Rare Disease // Life Cycle Management /

Manage external regulatory service providers to align with business objectives and support the development and maintenance of an effective regulatory affairs function. BSc or equivalent in a life science or legal discipline, with in-depth Regulatory Affairs experience across the EU and US from early

An experienced regulatory technologist with a minimum of 1 year in a cosmetics regulatory affairs. The regulatory team is focused on both regulatory compliance and customer needs to ensure products meet the highest standards of quality and commerciality. Managing an effective global regulatory horiz

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

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

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. Mainta

Job Overview: We are seeking an experienced Regulatory Affairs Consultant to support Clients France Regulatory Affairs (RA) team. Proven experience in Regulatory Affairs, preferably in cosmetics and/or commodities sectors. Job Title: Regulatory Affairs Consultant – Cosmetics/Commodities.

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

Regulatory Affairs Senior Manager - CMC, england. 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 Authorizatio

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

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

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

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

We are a forward-thinking regulatory affairs consultancy, DLRC Ltd takes the time to understand individual needs and find creative solutions for any regulatory challenge. We are looking to expand our Regulatory Affairs team and are currently looking for an experienced Regulatory Consultant to join u

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

The Senior Manager, Regulatory Affairs will be a strategic thinker, responsible for researching and assessing regulatory precedence and contributing to regulatory strategies for development of Compass Pathways investigational drug programs. This position assists in maintaining organization’s Regul

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. Role: Senior Principal Regulatory Affairs Specialist. Provide input to Regulatory

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

Head of Regulatory Affairs - MedTech. Get notified about new Head of Regulatory Affairs jobs in. A growing MedTech company is seeking an experienced Regulatory Affairs Leader.

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

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

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

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

Regulatory Affairs Team Lead (UK/EU). Specialise in managing regulatory affairs for EU products within the portfolio, ensuring adherence to regulations and standards. It includes harmonising regulatory efforts for EU products of the UK portfolio, with MAH under UK portfolio while regulatory oversigh

Are you an experienced regulatory affairs professional with deep expertise in Chemistry, Manufacturing, and Controls (CMC)? We’re looking for a Senior Manager to join a dynamic Medicine Development team supporting multiple projects from development through post-approval stages. Develop and execute

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

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

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

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

Provide for Westinghouse response and engagement to international regulatory bodies; industry and standards organizations based on alignment with the business unit and global regulatory affairs needs and. You will report to the Vice President, Global Nuclear Regulatory Affairs and be located at Spri

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

Provide for Westinghouse response and engagement to international regulatory bodies; industry and standards organizations based on alignment with the business unit and global regulatory affairs needs and. Manager you will direct and lead the nuclear regulatory affairs activities in support of Westin

We are unable to consider skilled or student visa applicants or offer sponsorship.CareTech is a person-centred Care Company, which provides quality of care to adults.We enable adults with complex needs to make their own life choices, and to develop confidence and independence to live, learn, thrive

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

Shift Pattern: 1 on 2 off basis including sleep ins.At Cambian, you’re not just working - you’re shaping futures, furthermore as a Team Leader, based within Bolton every moment you spend with our young people (ages 8–18) helps them feel safe, valued and supported.A simple "How was your day?",

As a Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and companionship and sharing great moments and memories too.It's a chance to bring your dedicatio

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

As a Bank Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and companionship and sharing great moments and memories too.It's a chance to bring your dedi

Warehouse Operative – Day Shift.Do not wait to apply after reading this description a high application volume is expected for this opportunity.Various working patterns available*.Avonmouth CDC, Cabot Park, Poplar Way West, Avonmouth, Bristol, BS11 0YW.Please check you can reliably commute to the w

As a Bank Housekeeping Assistant at a Barchester care home, you'll help to create a warm and homely environment that enables us to meet each resident's unique needs.Keeping the home clean and safe is no small task, which is why the role of a Bank Housekeeping Assistant is so important.The variety of

Operations Assistant - Blackburn (BB1 2QU) - Managed Services.We are Manged Services, a part of the Wolseley Group - a leading specialist trade merchant across the UK and Ireland.We pride ourselves in putting our people and customers at the heart of everything we do and best of all, provide opportu

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