regulatory associate jobs in Chester

You will receive a comprehensive induction, training, and awareness sessions to support your effectiveness in the role - A commitment to provide the time (circa 20 days per annum) and energy required is essential.

Job Title: Associate Product / Clinical Marketing Manager (Oncology Diagnostics) Status: Full Time Division: Commercial / Marketing Location: London-based (hybrid), remote (EU) considered for exceptional candidates Travel: Ability to travel up to ~25% of the time (primarily for conferences, partner meetings, and launch-related activities) Salary: Competitive Reporting: CEO, with structured,...

You will provide QA leadership across sterile manufacturing, oversee GMP elements of product development, including clinical material, and support a strong commitment to quality across site operations. Key technical responsibilities include: - Acting as a named Qualified Person on MIA and IMP licences, certifying and releasing commercial and clinical batches in line with UK/EU GMP and Annex 16.

Hartmann Young is partnered with a global, science-led SaaS provider supporting dietary supplement and nutraceutical companies with regulatory compliance, claims substantiation, and R&D insight platforms. This is a new business, hunter-focused Account Executive role selling subscription-based SaaS and associated services into the UK supplements market. The solutions support market entry,...

Our client is a firm member of the Electricity Transmission industry, specialising in strategical investment in offshore electricity transmission systems across Europe. We are looking for an experienced Substation/Transmission engineer, Senior wind turbine technician (with electrical and fault-finding experience) or other related engineer who is familiar with fault finding, electrical systems...

You will provide a technical lead for scripting, testing and delivering updates packs to the wider business using the automated update tool, Flamingo. - Attending the EE-Change Control Board (CCB), liaising with project teams to understand specifics, generating a bespoke test script and confirming suitability to associated baselines and System 42.

You will collaborate with design, operations, supply chain and FAL teams to optimise manufacturing processes and support on-site issue resolution. Key Responsibilities: - Produce and control Manufacturing Engineering data, technical instructions and documentation - Translate design intent to routings, BOMs, SOIs and STV calculations for production

You will provide strong, visible leadership to your team while ensuring the people we support receive outstanding, person-centred care that promotes independence, wellbeing, and positive outcomes. This is a varied and rewarding role, ideal for a values-driven leader who thrives in a hands-on environment and is passionate about supporting people with learning disabilities and autism.

You will collaborate with design, operations, supply chain and FAL teams to optimise manufacturing processes and support on-site issue resolution.

Residential Property Fee Earner / Conveyancer Location: Chester Contract: Full-time, permanent (37.5 hours per week) Salary: Competitive, dependent on experience Reports to: Team Head Overview Puro Associates are working with a leading regional law firm to recruit an experienced Residential Property Fee Earner for their Chester office. This is an excellent opportunity for a capable and motivated...

Main purpose of role: Financial modelling and analysisTreasury leadEffective support to the Investment Director (through insightful analysis and reporting and effective planning and administration) Ad-hoc financial and strategic projects Responsibilities Financial modelling and analysis Support the Financial Controller in delivering financial analysis and projections, strategic scenario...

Job Introduction Newly Qualified Dentist Are you a newly qualified dentist looking for the perfect next step after your DFT or DCT? At Rodericks Dental Partners, we understand the transition into your first role as an Associate Dentist, which is why we offer our bespoke FD+1 scheme—designed to provide the support, training, and confidence you need to thrive in both NHS and private...

You will often be included in projects that require you to collaborate cross-functionally. This is an exciting opportunity to join a successful company, with big ambitions for the future. If this sounds like you and you meet the requirements, please apply, we would love to hear from you.

Are you looking to further your career in residential property law? Our client, a leading and innovative law firm celebrated for its commitment to excellent client service, is seeking a skilled Conveyancing Executive to join their dynamic property team. This permanent, full-time position (Monday to Friday) at the Chester office. Key Responsibilities: - Manage a varied caseload of residential...

You will be provided you with a van, tool kit and your own scheduler to ensure your diary is both efficient and consistent. Duties & Responsibilities - Deliver, install and validate new equipment. - Carry out scheduled maintenance, site surveys and advise the customer of any additional costs incurred.

You will get a high level of autonomy and influence within a senior leadership team.

Company Description: Who We Are Scalian UK is a consultancy, specialising in digital systems and business management and performance, working in 11 countries, including France, Spain, Belgium, the UK, Germany, the USA, and Canada. Ranked in the top 10 engineering consulting firms in France, the Group provides services in industrial project management, quality management, supply chain...

You will receive a comprehensive induction, training, and awareness sessions to support your effectiveness in the role - A commitment to provide the time (circa 20 days per annum) and energy required is essential.

You will collaborate with design, operations, supply chain and FAL teams to optimise manufacturing processes and support on-site issue resolution.

You will provide QA leadership across sterile manufacturing, oversee GMP elements of product development, including clinical material, and support a strong commitment to quality across site operations. Key technical responsibilities include: - Acting as a named Qualified Person on MIA and IMP licences, certifying and releasing commercial and clinical batches in line with UK/EU GMP and Annex 16.