Associate Scientist, Analytical

General Information

Title: Associate Scientist

Department: Analytical

Site: Guildford

Reporting To: Team Leader

Position Summary

The Associate Scientist (Analytical) plays a key role in supporting research and development studies by performing analytical testing of pharmaceutical compounds, drug substance and drug product. This role is integral to the development of new drug formulations, ensuring accurate data generation to guide formulation design and process development. Working under the supervision of team leaders and senior scientists, the associate scientist is responsible for executing analysis through HPLC and GC in compliance with internal protocols and industry standards. The position involves HPLC method development and optimisation to support early and late‑stage pharmaceutical development. This role requires strong technical and organisational skills, attention to detail, and a commitment to scientific excellence in a fast‑paced, collaborative R&D environment.

Essential Functions

• Responsible for executing a variety of analytical techniques such as HPLC and GC to support the development of pharmaceutical drug products and assist in the day‑to‑day running of the laboratory in compliance with MedPharm’s QMS.
• Performing pre‑defined experiments according to internal standard operating procedures (SOP) (e.g., forced degradation of substance and product, saturated solubility, excipient compatibility and formulation stability).
• Support analytical method development and validation in accordance with ICH and FDA guidelines.
• Accurately document all experiments and results while demonstrating good laboratory practice (GLP), data integrity and quality.
• Analyze data using Empower and interpret results to support formulation development, stability studies and product release.
• Take an active responsibility for analytical work with respect to quality and compliance, particularly in the support of the analytical team.
• Collaborate with other departments, with oversight from supervisor where appropriate, attending meetings and contributing when appropriate.
• Aid the department’s method development and continuous improvement strategies.
• Adhere to Health and Safety and COSHH regulations and read relevant safety data sheets and risk assessments prior to undertaking work.
• Maintain training file (physical and MasterControl based) and follow appropriate health and safety guidance when using equipment or handling chemicals.
• Undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment.
• Conduct oneself in concordance with MedPharm Ethos, professionalism and confidentiality.

Key Relationships

• R&D Laboratory staff
• Analytical Team Leaders
• FD, PD and PT Study Managers
• Project Management team
• QC team
• Quality Assurance team

Education and Experience

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline.
• Familiarity with common analytical equipment and instrumentation (e.g., analytical balance, pH meter, HPLC, GC).

Knowledge, Skills, and Abilities

• Computer literate and knowledgeable in Microsoft Office Applications.
• Effective oral and written communication.
• Good observation skills and ability to document accurately.
• Strong ability to work in teams and collaborate.
• Good time management and organisational skills.
• Good knowledge and practical experience in analytical laboratory.

Physical Demands and Work Environment

• Occasionally required to lift up to 20 kg.
• Requires standing for extended periods.
• May be exposed to loud noise levels.
• May be exposed to hot or cold temperatures.

Other Duties

You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

Limitations and Disclaimer

The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.

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