Analytical Scientist

Analytical Scientist

  • Full Time
  • Reading
  • Posted 3 months ago

Main Purpose of the job

To co ordinate and implement the development of analytical methodologies for the analysis of pharmaceutical materials.
Assume responsibility for the analytical activities of assigned projects.
To assume responsibility for maintaining compliant processes with the analytical team and laboratory.
To perform the routine calibration of the lab equipment.
To routinely perform HPLC, FTIR, UV, Dissolution and KF analysis.
To routinely perform some or all of the following NGI, ED, and PSD.

Main Activities

  1. To provide Analytical expertise to IMP manufacture and Development, Screening & Formulation Development and Inhalation groups and business clients as required.
  2. To utilize the resources available to ensure that they contribute maximum effectiveness in achieving project objectives.
  3. To effectively manage multiple conflicting or simultaneous priorities.
  4. Ensure that GMP compliance is maintained in the Analytical laboratory.
  5. Maintain the IR, HPLC systems and GMP analytical system and associated documentation e.g. SOPs, Test Methods.
  6. To generate, assimilate and evaluate technical and scientific data generated and issue reports/protocols in line with project objectives.
  7. To develop knowledge and become expert in analytical techniques as required meeting business needs.
  8. To maintain your own training record and to discuss needs with your line manager.
  9. Undertake equipment and chemical ordering.
  10. To employ the principle of continuous improvement and a basis of teamwork in day to day activities with colleagues.
  11. To interact and exchange ideas within the group and with other scientists, to foster a creative culture
  12. Carry out duties in accordance with the companies’ health and safety policies
  13. Undertake any other duties as requested by management.
  14. Flexibility to work outside of normal hours and to do shift work as and when required by the company.
  15. Flexibility to take on other cross functional responsibilities based on company needs.

Qualifications

BSc, MSc or PhD
Pharmaceutical, Analytical Chemistry
3+ yrs
Supervisory, project and technical experience
Experience of working to cGMP
Understanding of investigational drug development process an advantage

Recruitment agencies need not apply

To apply please send your CV and covering letter to contactus@pharmaterials.co.uk.