Senior Scientist (Regulatory Bioanalysis) – Integrated Discovery & Development Services – Dundee

Concept Life Sciences is a knowledge based, science led business focused on delivering the expertise and capabilities our clients demand. We work in the pharmaceutical, biotechnology, food, environmental, agrochemical, petrochemical, chemical and consumer products sectors.  In order to deliver the science our clients demand, our business is focused on a number of core sectors. We support drug discovery and development in the pharmaceutical and biotechnology markets. We provide testing and specialist analytical services and consultancy to the food and environmental sectors. We provide toxicology services to the agrochemical, consumer products, chemical and pharmaceutical industries and materials chemistry services to the petrochemical industry.

The Role

A full time permanent opportunity is available on the Dundee site.   The Senior Scientist position is a pivotal role within the Analytical Sciences Team and will be focused on supporting regulatory (GLP) bioanalysis.  It is envisaged that the successful incumbent will be responsible for leading all activities relating to regulatory bioanalysis performed at the Dundee site and would work closely with the Team Leader of Analytical Sciences and Quality Assurance to ensure that work is resourced and executed to the highest scientific and regulatory standards.   The successful incumbent will also be expected to work with operational management, business development and senior management on the strategic development of the business.

Main Duties to:

  • In conjunction with the Team Leader of Analytical Sciences, plan and execute all regulatory (GLP) bioanalytical work supported at the Dundee site within agreed timelines.
  • Act as Study Director, Principal Investigator or Analytical Phase Manager (where appropriate) for regulatory studies (Bioanalysis and Formulation analysis).
  • Develop and validate chromatographic methods (LC-MS, LC-MS/MS, GC-MS, HPLC and GC) for bioanalytical support of GLP studies to current regulatory (FDA/EMEA) standards.
  • Develop and validate chromatographic methods (LC-MS, LC-MS/MS, GC-MS, HPLC and GC) for formulation analysis to current regulatory (FDA/EMEA) standards.
  • When required, assist in the study analysis of all bioanalytical and DMPK studies (regulatory and non-regulatory) performed within the Dundee site.
  • Contribute and author scientific publications.
  • Act as mentor to less experienced members of the organisation.
  • Operate in line with the company protocols and business strategy.
  • Author and assist in the review of SOPs and other business process documents.
  • Act as an ambassador for the business and in doing so proactively promoting the company brand and values both internally and externally.
  • Pro-actively identify opportunities for continuous improvement, profitability, quality and efficient ways of working.
  • Comply with health and safety requirements of the site as stated within company policy, procedure and practice.
  • Communicate effectively with colleagues throughout the business to share resources, technical knowledge and generally support all forms of business activity.
  • Generate a culture of collaboration and team work.
  • Assist with analysis planning and defining the scope of analysis in relation to instruments available.
  • Assist the Team Leader of Analytical Sciences and Lab Manager in reviewing instrument resource planning and utilisation in the labs.
  • Assist with initiating, managing and controlling contracts and managing commercial issues regarding laboratories and facility.
  • Assist the Team Leader of Analytical Sciences and Lab Manager in organising all repairs, maintenance of laboratory equipment and facilities.

Qualifications/Role Requirements

  • Bachelor’s degree in chemistry (or related discipline) essential.
  • Higher degree (Master or Doctorate) in related discipline highly advantageous.
  • Extensive knowledge and experience of chromatographic and mass spectrometric techniques essential.
  • Experience of acting as Study Director, Principal Investigator and/or Analytical Phase Manager essential.
  • Experience with Sciex equipment and Analyst software highly advantageous.
  • Experience of supporting bioanalytical studies within regulatory (GLP) framework essential.
  • Knowledge of market conditions, opportunities and competition desirable.
  • Understanding of customer base and commercial awareness also desirable.
  • Influencing and negotiation skills.
  • High-level interpersonal skills.
  • Robust time management capability.

Working Hours

  • 37.5 hours per week with flexibility required to meet the needs of the business.

Company Benefits

We offer a range of learning and development opportunities depending on the role, with all employees having access to a range of internally delivered training modules as standard.  In our science based roles we offer structured career progression, more details of which can be discussed during the recruitment process.  In addition to a competitive salary, we offer as a minimum: Pension scheme, Healthcare Cash Plan, Retail Discount scheme, Cycle to Work scheme, Childcare Vouchers, Discounted Gym membership rates and local Reward & Recognition schemes.