Associate Scientist, Analytical

MedPharm Ltd; Guildford; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading pharmaceutical research company in Guildford is seeking an Associate Scientist to support R&D through analytical testing. The role involves executing tasks using techniques like HPLC and GC, document experimental results, and collaborate closely with various departments. A Bachelor’s degree in Chemistry or a related field is essential. The ideal candidate will showcase strong technical skills, attention to detail, and a commitment to laboratory best practices in a collaborative environment.

Qualifications

• Familiarity with common analytical equipment and instrumentation.
• Strong ability to work in teams and collaboration.
• Good knowledge and practical experience in analytical laboratory.

Responsibilities

• Execute analytical techniques to support drug product development.
• Document all experiments and ensure compliance with good laboratory practice.
• Collaborate with other departments during research studies.

Skills

Analytical techniques

Communication skills

Team collaboration

Time management

Education

Bachelor’s degree in Chemistry or related discipline

Tools

HPLC

GC

Microsoft Office

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 compound, 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 and have a good understanding and demonstration of 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 your 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 your supervisor where appropriate. Attend meetings and contribute when appropriate.
• Aid in 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 your training file (physical and MasterControl based) and do not use any equipment or handle any chemicals without following the appropriate health and safety guidance.
• Undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment.
• Conduct yourself in concordance with the MedPharm Ethos, professionalism and confidentiality.

Key Relationships (examples: Depts or Individual positions that this position will be working closely with)

• 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 collaboration.
• Good time management and organisational skills.
• Good knowledge and practical experience in analytical laboratory.

Physical Demands and Work Environment

While performing the duties of this job, there may be certain physical demands required for the position.

• Occasionally required to lift up to 20kg.
• 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.