Healthcare jobs in Life Sciences

As QC analyst, you will be tasked with analysis of raw materials and finished product, playing a key part in ensuring compliance.

As a Technical Advisor you will be supporting customers by identifying and advising on novel solutions to challenges in the plant nutrition space. You will work to understand and identify gaps in the market, advising R&D functions on new areas of development.

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.

You will utilise your experience to analyse complex data sets,develop computational models, and build machine learning algorithms to support with the development of novel diagnostic platforms.

• The QC Technician is responsible for ensuring that medical devices meet regulatory, quality, and safety standards.
• Inspecting raw materials, in-process components, and finished products, performing tests, and maintaining compliance with industry regulations.

The Quality Manager will be tasked with leading the QA and QC teams, and acting as the SME for all Quality related queries across the business.

Great opportunity to join a global Animal health business as a National Contact Pharmacovigilance Manager.

Exciting opportunity to join a market leading global animal health business.

Leading a team of QA, QC and Regulatory professionals, this Head of Quality will be tasked with ensuring best practice across the business and implementing a quality strategy.

This is a unique opportunity for someone to lead the function, and implement real change with full authority and ownership of Quality.

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.

As the Organics Lab Manager you will oversee the organics function, leading a team of circa 20 scientist to deliver analytical data against agreed time-frames in a high-throughput lab, adhering to ISO standards at all times.

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

• Develop and implement cost-effective solutions to improve machinery efficiency, reliability and performance to minimise downtime
• Following planned schedules and troubleshooting reactive repairs, your work will include installation, commissioning, maintenance and modification of electrical and mechanical equipment and site service systems across the pharmaceutical production cycle, in-line with business needs

As the Inorganics Lab Manager you will oversee the inorganics function, leading a team of circa 20 scientist to deliver analytical data against agreed time-frames in a high-throughput lab, adhering to ISO standards at all times.

The Marketing CRM Executive will operate as a marketing and inside sales representative, working closely with the Marketing Manager to develop and execute demand generation strategies and digital marketing campaigns to drive growth in their dedicated market. This role will focus on nurturing and converting cold leads through personalised outreach and strategic CRM and LinkedIn management.

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.

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.

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.

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.

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.

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.

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.

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.