Life Sciences jobs in South East England

Are you a Life Sciences Professional relocating to the UK in the next few months? Michael Page Life Sciences recruit across the full drug life cycle from discovery to patient delivery, focusing on entry level to C-suite roles. We work with pharmaceutical, biotech, biopharma, and medical device companies, as well as CROs and consultancies across the UK.

As a Laboratory Technician, you will play a pivotal role in supporting the department's research endeavours by assisting in the execution of experiments, maintaining laboratory equipment and stocks, and preparing growth media. This role offers a unique opportunity to contribute to groundbreaking scientific discoveries that have a direct impact on the advancement of medical knowledge and patient care.

You will support with building AI models to aid discovery of novel cancer-cell receptors using knowledge of protein structures and sequences, which can then be validated to support with creating novel therapies.

You will be instrumental in delivery of analytical activities across a portfolio of new respiratory products, successfully leading projects as they progress into clinical studies and through to commercialisation!

As a Senior Manager (Analytical Team) you will lead on delivery of all analytical activities taking new products through to clinical studies and subsequently commercialisation. The main focus of research is respiratory treatments.

The client are a developing biotech undergoing expansion, with the aim to support in development of novel t-cell therapies.

You will utilise existing knowledge and a variety of research methods relating to cell line engineering, molecular techniques and screening assays to support development of novel t-cell therapies.

Working in the Project Management team as project owner, assisting with technical and commercial aspects. Running projects in a controlled and timely manner, utilising project management methodologies and planning in accordance with multi-site processes.

Research Assistant to contribute to the development of hydrogel drug delivery systems for the oral administration of small molecules and biologics.

Maintaining a focus on the value of patient-centric outcomes whilst ensuring that clinical programs have a innovative PRO/COA Strategy. Defining and overseeing the execution of strategies and guiding the development and validation of instruments in clinical trials and studies.

You will provide technical expertise and project management across bioanalytical activities, including oversight of outsourced bioanalysis at CROs for both clinical and pre-clinical drug development.

As a Clinical Research Associate, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs and medical devices experts to identify, select, initiate and close-out investigational sites for pre and post market studies, ensuring adherence to applicable regulations and principles of ICH-GCP.

Manage and coordinate all laboratory operations, including sample processing, data analysis, and quality control procedures. Oversee the allocation of resources, ensuring optimal utilization of equipment, supplies, and personnel.

• Ensuring all relevant EU & UK Regional and National licenses, and local infrastructure are in place to support the supply of commercial medicines working in close partnership with the Manufacturer and Marketing Authorisation holder.
• Ensuring local regulatory processes are in place for finished packs for commercial sale as per the Marketing Authorisation and Good Manufacturing standards (GMP).

Principal scientist in Drug Delivery - offer leadership on the development of drug delivery systems for the oral administration of small molecules and biologics, mentor junior members of staff and engage with external stakeholders.

My client is seeking a Sales Director to lead sales of CMO services/ API products to Pharmaceutical organisations by pursuing new business opportunities, establishing relationships with key partners, and developing and executing strategies to drive revenue growth in the UK. This is an individual contributor position but will work closely with the senior leadership team to implement business plans, evaluate potential partnerships and negotiate complex deals.

The Integrity & Compliance Manager/Associate Director will be responsible for supporting, managing and enhancing Most of World (MoW) implementation of the Global Integrity & Compliance Program (HCC focus).

Establishing clear policies and offering pragmatic, solutions-orientated guidance and program support to the AUA Integrity & Compliance Officer.

Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.

The purpose of this role is to make sure that the labelling is updated and compliant and meets the necessary trademark deadlines.

Responsible for life cycle management relating to variation submissions, renewals, labelling updates and preparing dossiers to meet national submission requirements. You will also be maintaining national aspects of Global Regulatory Systems.

Leading projects with small to medium complexity to develop and commercialise new products.

The Regulatory Affairs Director will report to the Global Head of Regulatory at Sinclair and will support the innovation, international and patient- centric strategies enabling simultaneous global access to our products.

Play a vital role in helping pharmaceutical and life sciences companies navigate the complexities of market access for their innovative products. Contribute to optimizing product reimbursement, formulary placement, and successful market entry, ensuring that patients can access the treatments they need. This position offers a unique blend of strategic thinking, data analysis, and collaborative problem-solving within a supportive and innovative environment.

Michael Page are partnering with a growing international company in the Life Science sector looking for a Financial Reporting Accountant to join their team.