Life Sciences jobs

We are seeking a detail-oriented finance candidate who is looking for a chance to explore something new and take on a new challenge. This is an excellent opportunity for someone who has started their career in finance and would like to work for a business where they can grow and develop their career.

Our client is a renowned organisation in the life sciences sector. Their primary focus is on pioneering research that will positively affect lives on a global scale and you will be working on a software that makes a real difference in the world.The company is based in Stockport and this is a hybrid role working in the office twice a week.

This role will oversee Quality operations across two manufacturing sites, leading the QA and QC teams. Our client is seeking a high performing Quality individual with background in a primary manufacturing Pharmaceutical facility.

You will be supporting the R&D function of the business developing novel biosensor technologies to support in the field of diagnostics.

Managing a team of Analysts and Senior Analysts, you shall enhance laboratory practices and promote a culture which is consistent with cGMP, cGLP and Health & Safety within a pharmaceutical laboratory environment.

Responsible for leading the Quality Control laboratory shift resources to achieve the required organisational throughput in a compliant and effective manner.

We are seeking an experienced and detail-oriented Quality Manager to oversee the quality assurance and regulatory compliance of our medical devices.

Developing, implementing, and maintaining quality management systems (QMS) in accordance with industry regulations.

We are seeking an EU Business Development Director to expand client relationships and introduce high-quality preclinical research products and services. The ideal candidate will have a life sciences background, strong sales skills, and the ability to travel within the EU and internationally.

We are seeking a Managing Director to lead a medical device manufacturing site, ensuring the delivery of high-quality, regulated products to the health care market. The role involves overseeing all functions, including production, quality, supply chain, and engineering, and commercial, while driving strategic initiatives and compliance with industry standards.

As a Project Manager, you will play a vital role in getting medicines to patients who have exhausted all viable options. You will be responsible for the setup, implementation, and management of individual Expanded Access Programs.

The Client Project and Resource Manager key roles and responsibilities encompass client project initiation through to close including delegating tasks, monitoring progress, budgeting, ensuring coordination among team members and collaboration.

This is an exciting time to join this client business, as they continue on their expansion. This role has the opportunity to become trainee RP, and so is a great chance for someone looking to develop.

As the main Quality representative in Switzerland, you will form part of the EU quality team. As this business seeks to expand its portfolio of products in EU, you will be helping shape the QMS and Quality Processes, as well as serving as FvP on the wholesale and import licenses.

As the Head of Laboratory Operations you will ensure smooth day-to-day running of technical and sample operations for the business spanning scientific development activities and lab operations.

Working in R&D as a Scientist you will be supporting the team with advancing the portfolio from ideation to commercialisation. This is a lab-based role where you will be developing, optimising and executing a range of electrochemical immunoassays.

This is a fantastic opportunity to lead the R&D and PD teams in development of novel biosensing technology. You will provide technical leadership as an SME and guide strategy to successfully deliver new products.

This role will take full ownership of site quality, leading a small team of QA and QC staff. The main responsibilities will be ensuring site GMP compliance, as well as being primary point of contact for customer and regulatory authorities.

This role will take full ownership of site quality. The client has excellent resource in the team, and we are looking for a strong leader to take strategically use resources available to drive excellent quality culture.

As a Scientist - Assay Development you will be supporting a number of allocated clinical trials utilising your virology expertise to develop, optimise and validate a range of assays and related techniques.

You will supervise the successful transfer of manufacturing processes from R&D to Manufacturing.

You will be responsible for optimising the performance of manufacturing systems.

This role is for a Laboratory R&D Manager for one of our key clients, requiring an experienced Laboratory Manager ideally from an Industrial setting. The successful candidate will be based at our clients site based in South Ayrshire.

The Managing Director will lead a Midlands-based medical device company, responsible for driving strategic growth, overseeing financial and operational management, and ensuring regulatory compliance. This is a hands-on leadership role, offering the opportunity to shape the future of a growing business with a global presence in the healthcare sector.

We are seeking a diligent and experienced Finance Manager to join our thriving life science division. The successful candidate will provide financial leadership and support to the accounting and finance department.

The QP/RP will be responsible for ensuring that quality processes and systems are compliant with the clients policies and GMP/GDP requirements. As QP you will ensure timely batch review of products to meet demand, alongside various other QMS, Risk Management, Training and RP Duties.

The Senior Director, Regulatory Affairs provides support to the Regulatory Affairs team across a range of projects as needed to support the group's activities, and works with the Vice President, Regulatory Affairs, for oversight of the team.

The QA and Regulatory Affairs Manager will play a fundamental role in maintaining continued regulatory compliance with standards and
medical device regulations. The ideal candidate will join a dynamic team launching innovative technology.

An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist to ensure product compliance within a leading beauty-tech manufacturer. The successful candidate will focus on ensuring compliance of the beauty tech devices with the EU MDR requirements, maintaining regulatory approvals, and supporting the company's regulatory strategy in the EU.

Are you a life science graduate? Or are you a healthcare professional with similar experience?

We are seeking a Senior RAQA Consultant with significant experience in Regulatory Affairs/Quality within SaMD/AIaMD. This role will work with a portfolio of medical device manufacturers so the successful candidate will be working with a varied portfolio of devices and stages.

The Head of RAQA will be a pivotal figure, steering the Regulatory Affairs and Quality Assurance department within a IVD medical device manufacturer start up. This individual will be responsible for ensuring the company meets industry standards and regulations.