Employed as a Development Analyst for a company specialising in the manufacture of controlled drugs, providing analytical support and advice to the R&D, Quality and Production departments.Responsibilities include: Raw Materials, In-process, R&D and Finished Products analysis.

Employed as a Quality Control Analyst for a company specialising in the manufacture of Controlled drugs, APIs and specialised pharmaceutical intermediates, providing cGMP support and advice to the Quality and Production departments.Responsibilities include: Raw Materials, Intermediates and Finished Products analysis, Sampling activities, cleaning verification and ensuring all documentation is compliant with cGMP guidelines

Employed as a Quality Control Analyst for a company specialising in High Potency API’s and Biologics including Antibody Drug Conjugates, providing cGMP support and advice to the Quality Control, Manufacturing and Process Development departments.Responsibilities include: Raw Materials, In-process and Final Product sample analysis, operation and manipulation of API’s within a high potency containment suite, data review, coordinating external sample analysis, conducting laboratory investigations and ensuring all documentation is compliant with cGMP guidelines.

Employed as a Senior Quality Control Analyst for a company specialising in Semi-solid capsule products, providing cGMP support and advice to the Formulation Development, Analytical Development and Production departments.

Senior Analyst – Analytical Support:Employed as a Senior Analyst in a customer focused team, providing Analytical support, expertise and management of Analytical activities, at every stage of Pharmaceutical Development. Responsibilities include: Sample prep and analysis, method development and validation, conducting excipient compatibility studies, providing analytical support for cGMP Manufacturing campaigns and stability protocols, authoring Protocols and Reports, mentoring junior team members, providing a point of contact for customers and ensuring all documentation is compliant with current GMP guidelines.

Employed as an Analytical Research and Development scientist, working on the development and assessment of novel inhalation formulations for the treatment of respiratory conditions such as Asthma and Chronic obstructive pulmonary disease (COPD).

Worked as a Quality Control analyst in the Active Pharmaceutical Ingredients (API), laboratory conducting routine testing to cGMP standards and under GLP conditions.

Employed as a Quality Control analyst, conducting routine testing of pharmaceuticals, including Bulk, Finished goods and Stability drug products, to cGMP standards.