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Junior Regulatory Coordinator

Location: West Yorkshire

Salary: £28,000 - £30,000 + Benefits

Our client is seeking a Junior Regulatory Affairs Administrator to join their Technical team based in Bradford.

This is an excellent opportunity for an organised and detail-focused individual looking to develop a career within Regulatory Affairs. Working alongside an experienced Regulatory professional, you will receive full training and support whilst gaining exposure to a broad range of UK, EU and international compliance requirements.

This is a predominantly desk-based role and would suit someone who enjoys working with data, systems and technical information whilst supporting the wider business on regulatory and compliance matters.

Key Responsibilities

Support regulatory and compliance activities across a range of products and packaging formats.Collect, maintain and process technical and regulatory data to ensure compliance with relevant legislation.Assist with the management and maintenance of product and packaging information.Maintain internal databases and ensure information remains accurate, current and readily accessible.Support the preparation and completion of compliance documentation for customers and external stakeholders.Assist with the completion of technical questionnaires and customer information requests.Monitor and maintain regulatory records and documentation.Support the wider business by communicating updates relating to regulatory requirements.

About You

We are looking for someone who is:

Highly organised with exceptional attention to detail.Confident using Microsoft Excel and other IT systems.Comfortable working with large volumes of data and technical information.Able to prioritise workloads and manage multiple tasks effectively.A strong communicator with excellent administrative skills.Keen to learn and develop within a regulatory and compliance environment.

Experience & Qualifications

A degree in Chemistry, Environmental Science, Regulatory Affairs or another scientific discipline would be advantageous.Previous experience within a regulatory, compliance, technical administration or similar office-based environment is desirable.Recent graduates with strong organisational and IT skills are encouraged to apply.Experience within manufacturing, chemicals, FMCG or another regulated industry would be beneficial but is not essential.

What's on Offer?

Salary of £28,000 - £30,000 depending on experience.Company pension scheme.24 days annual leave.Optional private medical insurance.Genuine progression opportunities within Regulatory Affairs.The opportunity to learn from an experienced regulatory professional.Flexible working arrangements may be considered for the right candidate.

This is an exciting opportunity to join a successful and growing organisation and develop a long-term career within Regulatory Affairs and Compliance.

To apply, please submit your CV for immediate consideration.

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Automation & CSV Engineer (Permanent) - West Yorkshire

Pharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth Opportunity

An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector.

This role is ideal for an engineer who enjoys working at the intersection of automation, validation, digital systems, and manufacturing operations. You'll play a key role in supporting critical production systems, driving continuous improvement initiatives, and ensuring compliance across computerized and automated processes.

Key Responsibilities

Support and maintain automation and control systems across manufacturing operationsTroubleshoot equipment and process-related automation issuesParticipate in computerized system validation (CSV) activities within a GMP-regulated environmentAssist with qualification, commissioning, and lifecycle management of automated systemsSupport continuous improvement and process optimization projectsCollaborate with engineering, production, quality, and external vendorsMaintain technical and validation documentation in line with regulatory expectationsContribute to data integrity and compliance initiativesProvide technical support and training to operational teams

Ideal Background

Degree qualified in Automation, Electrical, Electronics, Mechatronics, or related Engineering disciplineExperience working with PLC, HMI, SCADA, or industrial control systemsExposure to regulated industries such as pharmaceuticals, biotech, medical devices, or food manufacturing preferredUnderstanding of GMP and computerized system validation principlesStrong troubleshooting and problem-solving skillsAbility to work both independently and within cross-functional teamsExcellent communication and technical documentation abilities

Desirable Experience

PLC/SCADA programming or supportSystem integration projectsEquipment qualification or validation activitiesKnowledge of data integrity and regulatory compliance requirementsExperience supporting utilities, manufacturing systems, or process equipment

What's on Offer

Opportunity to work in a modern, highly automated manufacturing environmentExposure to cutting-edge pharmaceutical technologiesCareer progression within engineering and digital manufacturingCollaborative and technically focused cultureCompetitive salary and benefits packag

This is an excellent opportunity for an ambitious engineer looking to develop within a fast-paced and growing technical operations environment.

For a confidential discussion or to learn more, please contact Simon Fowler on

+44 (0)1925 239 725 or

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