Associate Scientist, Analytical

MedPharm; Guildford; On-site; GBP 32,000 - 52,000; Full time

Job summary

MedPharm in Guildford seeks an Associate Scientist (Analytical) to perform analytical testing of pharmaceutical compounds, drug substance and drug product, supporting early and late development. You will execute HPLC and GC analyses and contribute to method development and validation in line with ICH/FDA guidelines.

Under supervision, you will document results, ensure data integrity and GLP compliance, collaborate with R&D and quality teams, and help drive continuous improvement while

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline.
• Familiarity with analytical equipment such as HPLC and GC.

Responsibilities

• Execute analytical techniques such as HPLC and GC to support development of pharmaceutical drug products.
• Assist in method development, validation, and adherence to SOPs and internal QMS.
• Document experiments accurately and uphold GLP and data integrity standards.
• Analyze data and interpret results to support formulation development and product release.
• Collaborate cross-functionally with other departments under supervisor guidance.

Skills

Microsoft Office

Effective communication

Documentation

Teamwork

Time management

Analytical laboratory

Education

Bachelor’s degree in Chemistry or related

Tools

HPLC

GC

Job description

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. The 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.
• Perform predefined 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 and demonstrate 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.
• Assist the progression of the study by collaborating with other departments, with oversight from the supervisor where appropriate; attend meetings and contribute when appropriate.
• Aid the department’s method development and continuous improvement strategies.
• Adhere to Health and Safety and COSHH regulations and review relevant safety data sheets and risk assessments before undertaking work.
• Maintain the training file (physical and MasterControl based) and not use any equipment or handle any chemicals without following the appropriate health and safety guidance.
• Perform general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment.
• Conduct oneself in concordance with the 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 teamwork and collaboration skills.
• 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.
• Must stand 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.