compliance associate jobs in Wirral

A leading biopharmaceutical company is seeking an experienced Associate Director, PDQ Qualified Person to join their Moreton site in the UK. The role entails ensuring compliance with regulatory standards, qualifying products for release, and providing quality issue consultation. Candidates should possess a science degree and experience as a UK Qualified Person. This position offers opportunities...

Your future as an Associate Dentist at mydentist Your future, your schedule You’ll be joining us at our Victoria Road, New Brighton practice. We have surgery space available Monday - Wednesday and Friday from 9:00am - 17:30pm. Your future at our Victoria Road, New Brighton practice 4 surgery practice; 3 clinicians with a team of 4 qualified dental nurses and 1 student dental nurse There are...

This highly regarded Housing Association based in the North West is now seeking to appoint a new Director of Governance & Assurance on a full time, permanent basis. Reporting directly to the Deputy Chief Executive, you'll serve as Company Secretary and nominated Data Protection Officer. This is a pivotal leadership role where your expertise will shape the future of governance, assurance and...

You will be responsible for the contract and commercial management of multiple residential new build schemes, ensuring projects are delivered safely, on time, within budget, and to required quality and compliance standards. Key Responsibilities

You will be responsible for delivering include monthly management accounts, consolidated group accounts ,statutory returns, and quarter-end submissions.

You will also act as the main point of contact for external auditors and ensure adherence to Health & Safety policies and procedures.

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 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.

Job Description Working at the Liverpool site as part of the Global SA team under general direction from the Snr Manager of Sterility Assurance, this candidate is to provide sterility assurance support for the Seqirus Liverpool and relevant CMO Sites. They will support (and deputise for) the Snr Manager and will focus their efforts to ensure that from an aseptic perspective, the day to day...

Job Description Sureserve provide market leading compliance and energy services across the UK, with close to 4000 employees working from over 20 offices. Sureserve is a trusted partner for housing associations, local authorities, and residents, delivering high-quality compliance and energy services. Our focus on energy efficiency, safe and compliant homes, and enhanced quality of life makes us...

Job Description Overview Red Sky Personnel are seeking an experienced Ganger to oversee a gang on a civil engineering project in the Thornton Hough area. The successful candidate will be responsible for leading site operations, ensuring works are carried out safely, efficiently, and in accordance with project requirements. Location: Thornton Hough, Wirral Start Date: 09 February 2026 Duration:...

You will lead on financial strategy, budgeting, forecasting and reporting, oversee cash flow and statutory compliance, and provide clear, timely insight to support decision-making.

You will be strategic, highly analytical and detail-focused, while maintaining a clear view of the bigger picture.

You will be responsible for producing accurate panel designs, managing documentation, supporting production, and acting as a key technical point of contact for internal teams and external stakeholders.

You will play a critical role in standardising processes, managing diverse stakeholder needs, and embedding a project and process-driven mindset. Entrepreneurial thinking, commercial awareness, and an eye for innovation are essential to this role as the company grows and scales.

Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to...

OverviewRed Sky Personnel are seeking an experienced Ganger to oversee a gang on a civil engineering project in the Thornton Hough area. The successful candidate will be responsible for leading site operations, ensuring works are carried out safely, efficiently, and in accordance with project requirements.Location: Thornton Hough, WirralStart Date: 09 February 2026Duration: End of February...

A leading pharmaceutical company seeks an Associate Director, PDQ Qualified Person for their Moreton site. This permanent role involves UK certification of Investigational Medicinal Products, overseeing GMP activities, and leading quality compliance efforts. Candidates should possess a science degree and demonstrable experience as a UK Qualified Person. Strong leadership and quality management...

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

Working with Us Challenging. Meaningful. Life-changing. Bristol Myers Squibb offers work that transforms the lives of patients and the careers of those who do it. Opportunities to grow and thrive exist alongside high-achieving teams. Position : Associate Director, PDQ Qualified Person (permanent contract) – Moreton site. Reports to the Director of PDQ. This is a non-management role within the...