Regional Supervisor, Global Operations UK/EU

Catalent Pharma Solutions; Bathgate; On-site; GBP 42,000 - 56,000; Full time

Benefits offered by this job

Pension scheme matching 7.5%

Life assurance

BUPA private medical insurance

Generous holiday entitlement

LinkedIn Learning subscription

On-site parking

Job summary

Catalent Pharma Solutions in Bathgate, UK is seeking a Regional Supervisior to lead and develop regional MDM, GOPP, and GOPD teams, ensuring workloads, quality, and compliance meet the highest standards.

You will collaborate with global teams to drive continuous improvement, manage master data activities, and support audits and CAPA processes while fostering a high-performing, customer-focused culture.

Qualifications

• Experience in MDM, supply chain, clinical trial materials, pharmaceutical operations, or a regulated environment.
• Leadership or supervisory experience.
• Knowledge of GxP, SOPs, change controls, CAPAs, and compliance requirements.
• Strong communication and stakeholder management skills.
• Highly organised with excellent attention to detail.

Responsibilities

• Lead and develop regional MDM, GOPP, and GOPD teams.
• Manage workloads, KPIs, quality, and operational performance.
• Oversee accurate master data, pre-production, and pre-distribution activities.
• Ensure compliance with SOPs, GxP standards, and regulatory requirements.
• Support audits, change controls, deviations, and CAPA activities.
• Provide technical guidance and training to team members and collaborate with global teams.

Skills

MDM experience

Supply chain experience

Leadership

GxP knowledge

SOPs & CAPAs

Communication

Stakeholder management

Attention to detail

Decision making

Education

Bachelor's degree or equivalent

Tools

Microsoft Excel

Microsoft Word

PowerPoint

ERP systems

MDM systems

Job description

Position Summary

With nearly 25 years of experience, our Bathgate location in Scotland, UK is an integral part of Catalent's European clinical supply services network. This 141,000 sq. ft. facility has a comprehensive range of capabilities to support sponsors' studies throughout the UK, Europe and beyond, including clinical supply management, FastChain® demand-led supply, clinical-scale commercial packaging, and QP release services. We have high-speed, automated primary packaging for blisters, as well as semi-automated primary packaging for bottles. We offer packaging design services on site, as well as secondary packaging and clinical labeling services.

We have an opportunity for a Regional Supervisior, Global/ UK/EU to join our team. In this role, you will lead and support regional teams to ensure effective workload management and operational excellence. You will oversee master data activities, maintain compliance, and drive process improvements. This position offers the chance to collaborate globally and foster a high-performing team culture.

Shift & Location

Shift: Monday - Friday 37.5 hours p/w. Location: Bathgate, UK. 100% Onsite.

The Role

Lead and develop regional MDM, GOPP, and GOPD teams. Manage workloads, KPIs, quality, and operational performance. Oversee accurate master data, pre-production, and pre-distribution activities. Ensure compliance with SOPs, GxP standards, and regulatory requirements. Support audits, change controls, deviations, and CAPA activities. Provide technical guidance and training to team members. Collaborate with global teams to ensure consistent processes and business continuity. Drive continuous improvement initiatives to enhance quality and efficiency. Partner with cross-functional stakeholders to resolve issues and meet business objectives. Foster a high-performing, collaborative, and customer-focused team culture.

The Candidate Minimum Requirements

Experience in MDM, supply chain, clinical trial materials, pharmaceutical operations, or a regulated environment. Previous leadership or supervisory experience. Knowledge of GxP, SOPs, change controls, CAPAs, and compliance requirements. Ability to manage multiple priorities and meet deadlines. Strong communication and stakeholder management skills. Highly organised with excellent attention to detail. Ability to work independently and exercise sound judgement. Proficient in Microsoft Office, particularly Excel, Word, and PowerPoint. Bachelor's degree in a relevant discipline or equivalent industry experience.

Preferred Skills & Background

• Experience with ERP, master data, clinical supply, or distribution management systems.
• Pharmaceutical, biotechnology, clinical supply, or other regulated industry experience.
• APICS certification.
• Experience working within global teams and supporting operations across multiple regions and time zones.
• Flexibility to support occasional travel and business-critical activities outside standard working hours.

Why You Should Join Catalent

With nearly 25 years of experience, our Bathgate location in Scotland, UK is an integral part of Catalent's European clinical supply services network. This 141,000 sq. ft. facility has a comprehensive range of capabilities to support sponsors' studies throughout the UK, Europe and beyond, including clinical supply management, FastChain® demand-led supply, clinical-scale commercial packaging, and QP release services.

Competitive Salary & Benefits

• Competitive Salary – Reflecting your experience and skills.
• Benefits – a pension scheme matching up to 7.5% and life assurance.
• Enjoy BUPA private medical insurance, a generous holiday entitlement that increases with tenure, and the option to trade leave.
• Career Development – Access high-quality training, mentoring, and cross-functional opportunities within Catalent's global network. Benefit from a subscription to LinkedIn Learning, providing access to 10,000+ online courses.
• Health & Wellbeing – Includes an employee assistance programme, on-site canteen facilities, and an active safety and "Patient First" culture.
• Join Employee Resource Groups that foster a diverse and inclusive workplace.
• Plus, participate in charitable activities.
• Excellent Location – Just a few minutes’ drive from J3A of the M8, with free on-site parking.

About Catalent

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. We are a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives.

With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.

Equal Opportunity and Accessibility

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.