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Regulatory Scientist

2 months ago


Nottingham, Nottingham, United Kingdom Cellomatics BioSciences Ltd Full time

Cellomatics BioSciences Ltd. is a rapidly growing Contract Research Organisation (CRO) providing pre-clinical laboratory services to support the drug development programmes of Biotech and Pharmaceutical companies.

About the Role:

We are seeking an experienced Immuno-oncology Scientist to join our team at 10 Colwick Quays Business Park, Nottingham, UK. As a key member of our scientific team, you will be responsible for:

  • Selecting and Developing Immuno-oncology In Vitro Models: Design, execute, and troubleshoot in vitro immunology/immuno-oncology related assays.
  • Conducting Laboratory Work: Undertake laboratory work as required and be responsible for drafting SOPs, COSHH as relevant.
  • Preparing and Presenting Complex Scientific Information: Prepare and present complex scientific information to internal and external stakeholders.
  • Sharing and Contributing Scientific Expertise: Share and contribute scientific and technical expertise with matrixed team members.
  • Analyzing and Communicating Scientific Findings: Clearly analyze and communicate scientific findings in written and verbal form.
  • Staying Up-to-Date with Regulatory and Scientific Guidelines: Keep abreast of regulatory and scientific guidelines and industry expectations and contribute to the establishment and delivery of appropriate services within the department.
  • Providing Expert Advice: Provide expert advice on specific projects to colleagues and clients, maintaining awareness of current trends, issues, and developments.
  • Leading Problem Resolution: Taking a lead role in problem resolution and ensure that the conduct and reporting of the project complies with the client requirements including review of data and production of scientific reports.
  • Maintaining Stock and Resources: Maintain stock of reagents and consumables required for client projects.
  • Improving Quality and Productivity: Continually seek to identify opportunities for and lead improvements in quality, productivity, and automation and the introduction of new tests and techniques.
  • Assisting in Accreditation and Business Development: Assist the scientific team in securing relevant accreditations and assist in obtaining new business and in client inspection visits.
  • Developing and Maintaining Training Programs: Develop and maintain training programme modules in own area of expertise to meet client requirements and realise individual potential.
  • Implementing New Equipment and Procedures: Assist in the implementation of new equipment, IT systems, and procedures/processes.

Requirements:

  • Education: A degree in immuno-oncology or immunology (or closely related field) is required.
  • Experience: 2 years post-graduate experience in biotechnology and/or pharmaceutical drug development.
  • Skills and Qualifications: Strong background in immunoassay and in vitro model development and execution, demonstrated ability to independently design, execute, and interpret scientific experiments, proven experience working in a diverse and highly matrixed, fast-paced collaborative team environment, experience of working with primary human/animal cells, ability to work to strict deadlines and multi-tasking, excellent oral and written communication skills, and proven experience of presenting complex information to clients.

What We Offer:

Our benefits package includes a competitive salary, discretionary bonus, pension contribution, flexible working options, and access to an on-site Cafe.