120 Regulatory Support jobs in the United Kingdom

Membership body seeks a Regulatory Support Lead to assist in the review of conduct regulations.

You will undertake legal and policy work to assist changes to the enforcement team’s disciplinary policies, procedures and guidance relating to the investigation of professional misconduct by members.

This is an exciting role – with exposure to the senior management team. You will be leading a high-profile project, with all the responsibility and kudos that comes with that.

You will be working from home.

For more information, please apply to this advert.

Please note our advertisements use PQE/salary levels purely as a guide. However we are happy to consider applications from all candidates who are able to demonstrate the skills necessary to fulfil the role.

At LAW Absolute we endeavour to respond to all applications within 48 hours. However due to the volume of applications we receive we may not be able to respond to every candidate individually.

If you have not heard from us within a 48 hour timeframe your application has not been successful and your details have not been retained. LAW Absolute acts as an employment business for temporary recruitment and as an employment agency for fixed term contract and permanent recruitment.

Regulatory Support Officer

£26,939 - £28,074 per annum plus pay award, pro rata

21.5 hours per week

Permanent

Witney

Make a difference in your community!

Are you passionate about food safety and protecting public health or do you have experience working in catering and hospitality, if so we would love to hear from you.

This is a great opportunity for someone who wants to use their transferable skills and.

• Preparing and managing regulatory documentation for a diverse product portfolio.
• Organising and maintaining compliant regulatory records as per industry standards.
• Tracking and reporting regulatory project progress to stakeholders.
• Keeping abreast of regulatory changes and communicating updates to internal teams.
• Monitoring industry trends to ensure ongoing compliance with pharmaceutical regulations.
• Supporting client communications related to regulatory processes and updates.

• A Bachelor’s degree in a scientific, healthcare, or related field.
• Proven experience in Regulatory Affairs within the pharmaceutical industry.
• Exceptional organisational skills and meticulous attention to detail.
• Strong written and verbal communication skills.
• Adaptability to evolving regulatory requirements.
• A collaborative spirit, excelling in team-oriented settings.
• Proficiency in standard office software (e.g., Microsoft Word, Excel, Outlook).
• A drive for professional development in regulatory affairs.
• Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).

• Experience with regulatory submissions for new products or post-market changes.

What does 'family business' mean to you?

For some, it's code for small, for others it is a collaborative and friendly space.

The truth - it's usually both.

Family, small to midsized pharmaceutical companies look after their staff. You become part of their community, their culture, and the way they do things.

In our experience, staff at family run SMEs experience longer levels of employment than at large global corporations, and are often compensated well over time for their rewards.

Which is why, I am delighted to be representing a leading (family run) pharmaceutical manufacturing organisation based near Watford in the UK.

This amazing company are going through a great transformation that should ensure the company's future for generations to come, and as part of that they are looking for reliable, professional and hard working Regulatory Affairs professionals.

As part of this expansion, our client is looking for someone with 5+ years experience in Pharmaceutical Regulatory Affairs (ideally in a similar style of company, but they are open to people from all different pharmaceutical organisations).

You need to have a hard working attitude, good attention to detail, and you need to be able to work well with your team. Your experience in eCTD manager and document management tools will be valued, and you will need knowledge of global Regulatory requirements and guidelines (MHRA, EMA and ICH).

This is a site based role near Watford (5 days per week) and would suit someone looking for a company they can grow with, and build with, and that will give them huge career tragectory in a culture that is supportive and dynamic.

Interested? Apply Now!

• The Regulatory Affairs Consultant EMEA (Self Care) is responsible for the development of regulatory strategies across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product development teams within the Self Care franchise.
• Evaluates and coordinates the regulatory deliverables for medicines and food supplements, within their geographical and/or brand area of responsibility.
• Prepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.
• Tracks the status of applications under regulatory review and provides updates to the regulatory team.
• Works with local and regional regulatory colleagues to develop global and/or regional regulatory strategies, coordinating regulatory actions and results and develops global/regional dossiers to support local review processes

• Relevant Bachelor's Degree or higher in Life Sciences, Chemistry, Pharmacy
• Expertise across a broad spectrum of Regulatory classifications in particular medicine and food supplements in EMEA region
• Strong knowledge of regulatory frameworks and external environments, and the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory/medical/safety/quality requirements in the markets of relevance.
• In-depth knowledge of the business, organizational goals, Regulatory Affairs function, and cross functional business partners to make informed business decisions and create and execute business strategies. Ability to represent RA function on cross-functional teams and governance forums.

Location: Essex

Salary Package : 46,142 - 52,514 per annum

Benefits for the Regulatory affairs Officer :

• • Permanent full-time role with stability and employment benefits
    
  • Prestigious local authority
  • Work for a special project within

    DEPARTMENT FOR NEIGHBOURHOODS AND ENVIRONMENT

    PUBLIC PROTECTION

  • Local government pension scheme
  • Generous annual leave
  • Flexible working
  • Training and development

NonStop Consulting is currently working with UK government authority to recruit a Regulatory Affairs Officer for one of the local councils in Essex.

Responsibilities of Regulatory Affairs Officer:

To carry out a range of complex Regulatory Services duties including taking lead responsibility for statutory functions involving projects / inspection programmes / major or complex investigations / supervising other staff members / regional coordination work / council's corporate projects (business partnerships etc)

Please apply if:

- you have experience applying national/regional/local policies to regulatory services work
- evidence of CPD (Continuous Professional Development)
- complex housing disrepair issues/ complex investigations

- you have Professional Qualification in a relevant area of Regulatory Services

You can send your CV directly to me at (url removed)

If you believe this opportunity isn't the right fit for you but know someone who would be a great match, we would love to hear from them! We offer a 200 referral bonus through our referral scheme.

• The Regulatory Affairs Consultant EMEA (Self Care) is responsible for the development of regulatory strategies across the EMEA region, and globally as relevant, providing regulatory input and technical guidance on regulatory requirements to product development teams within the Self Care franchise.
• Evaluates and coordinates the regulatory deliverables for medicines and food supplements, within their geographical and/or brand area of responsibility.
• Prepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.
• Tracks the status of applications under regulatory review and provides updates to the regulatory team.
• Works with local and regional regulatory colleagues to develop global and/or regional regulatory strategies, coordinating regulatory actions and results and develops global/regional dossiers to support local review processes

• Relevant Bachelor's Degree or higher in Life Sciences, Chemistry, Pharmacy
• Expertise across a broad spectrum of Regulatory classifications in particular medicine and food supplements in EMEA region
• Strong knowledge of regulatory frameworks and external environments, and the ability to apply these to regulatory solutions throughout the product lifecycle.
• Solid understanding of regulatory/medical/safety/quality requirements in the markets of relevance.
• In-depth knowledge of the business, organizational goals, Regulatory Affairs function, and cross functional business partners to make informed business decisions and create and execute business strategies. Ability to represent RA function on cross-functional teams and governance forums.

Location: Essex

Salary Package : 46,142 - 52,514 per annum

Benefits for the Regulatory affairs Officer :

• • Permanent full-time role with stability and employment benefits
    
  • Prestigious local authority
  • Work for a special project within

    DEPARTMENT FOR NEIGHBOURHOODS AND ENVIRONMENT

    PUBLIC PROTECTION

  • Local government pension scheme
  • Generous annual leave
  • Flexible working
  • Training and development

NonStop Consulting is currently working with UK government authority to recruit a Regulatory Affairs Officer for one of the local councils in Essex.

Responsibilities of Regulatory Affairs Officer:

To carry out a range of complex Regulatory Services duties including taking lead responsibility for statutory functions involving projects / inspection programmes / major or complex investigations / supervising other staff members / regional coordination work / council's corporate projects (business partnerships etc)

Please apply if:

- you have experience applying national/regional/local policies to regulatory services work
- evidence of CPD (Continuous Professional Development)
- complex housing disrepair issues/ complex investigations

- you have Professional Qualification in a relevant area of Regulatory Services

You can send your CV directly to me at (url removed)

If you believe this opportunity isn't the right fit for you but know someone who would be a great match, we would love to hear from them! We offer a 200 referral bonus through our referral scheme.

• Preparing and managing regulatory documentation for a diverse product portfolio.
• Organising and maintaining compliant regulatory records as per industry standards.
• Tracking and reporting regulatory project progress to stakeholders.
• Keeping abreast of regulatory changes and communicating updates to internal teams.
• Monitoring industry trends to ensure ongoing compliance with pharmaceutical regulations.
• Supporting client communications related to regulatory processes and updates.

• A Bachelor’s degree in a scientific, healthcare, or related field.
• Proven experience in Regulatory Affairs within the pharmaceutical industry.
• Exceptional organisational skills and meticulous attention to detail.
• Strong written and verbal communication skills.
• Adaptability to evolving regulatory requirements.
• A collaborative spirit, excelling in team-oriented settings.
• Proficiency in standard office software (e.g., Microsoft Word, Excel, Outlook).
• A drive for professional development in regulatory affairs.
• Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).

• Experience with regulatory submissions for new products or post-market changes.