272 Inspection Manager jobs in the United Kingdom

Inspection Manager

Pioneering New Division

Up to £64,000 + 20% Bonus + Company Vehicle + fantastic Package with 12% Pension

Liverpool HO + UK Site Travel

Engineering / Asset Integrity / Heavy Industry

Are you ready to put your stamp on something big?

We're working exclusively with a major UK industrial enterprise at a pivotal point in their growth. They're launching a brand-new Inspection Division, an area set to become a cornerstone of their UK operations, and they're looking for an experienced Inspection Manager to lead from the front.

This isn't just a job, it's a career-defining opportunity . You'll have the autonomy to shape, scale, and elevate a division backed by serious investment, board-level support, and a forward-thinking leadership team. If you're a qualified inspection professional with a passion for people leadership, technical excellence, and delivering impact-this could be the platform you've been waiting for.

What You'll Be Doing

• Leading and managing the newly formed Inspection Division
• Ensuring high-quality inspections and technical reporting across multiple UK sites
• Preparing and delivering commercial proposals to external clients
• Managing invoicing and service delivery for third-party work
• Working closely with senior stakeholders to build long-term client relationships
• Driving innovation, standards, and continuous improvement

What We're Looking For

Essential:

• A recognised inspection qualification such as EEMUA 159 , API 570 , API 510 , or equivalent
• Experience in an asset integrity, inspection, or maintenance engineering environment
• Previous leadership or management experience
• Strong stakeholder and client engagement capability
• Willingness to travel across UK sites with occasional overnight stays

The Package

• Basic Salary: Up to £4,000
• Achievable 20% Annual Bonus
• Company Vehicle (small van) + Paid Travel Expenses
• 0 Overnight Bonus
• 26 Days Annual Leave + Bank Holidays
• Private Medical Insurance
• Life Assurance
• 9% Employer Pension Contribution (3% employee)
• Free On-Site Parking

Why This Role?

This is your chance to build something from the ground up , make strategic decisions, and be known as the individual who established a highly respected and commercially successful inspection division within a nationally recognised organisation. The potential for growth-both for the division and your career-is immense.

You'll join a team that values technical integrity, innovation, and people development , and you'll be empowered to make decisions that matter. This isn't a back-office role-it's frontline leadership with high visibility and tangible results.

Ready to Take the Lead?

Apply now or get in touch for a confidential conversation. We are representing our client exclusively on this critical hire, and interview slots are already being scheduled for early September . Let's talk about how this could be your next big move.

At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions.

We recruit for companies that operate in the following industries: Defence Equipment, Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy.

Our commitment:

Equal opportunities are important to us. We believe that diversity and inclusion at Morgan Ryder Associates are critical to our success as DE&I positive company, so we want to recruit, develop, and keep the best talent. We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristic.

Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.

Inspection Manager

Pioneering New Division

Up to £64,000 + 20% Bonus + Company Vehicle + fantastic Package with 12% Pension

Liverpool HO + UK Site Travel

Engineering / Asset Integrity / Heavy Industry

Are you ready to put your stamp on something big?

We're working exclusively with a major UK industrial enterprise at a pivotal point in their growth. They're launching a brand-new Inspection Division, an a.

• 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.