General Information
Title: Associate ScientistDepartment: AnalyticalSite: GuildfordReporting To: Team Leader
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 organizational skills, attention to detail, and a commitment to scientific excellence in a fast-paced, collaborative R&D environment.
Essential Functions
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
Education and Experience
Knowledge, Skills, and Abilities
Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
Example:
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.

Bringing a topical or transdermal therapy from concept to patient is complex. Scientific uncertainty, regulatory expectations, and manufacturing realities all shape the path forward.
MedPharm supports companies navigating that complexity with focused expertise in topical and transdermal drug development and manufacturing.
From formulation and preclinical research to clinical trial supply and commercial manufacturing, we work alongside partners to advance programs efficiently, strategically, and responsibly.
Our approach is grounded in decades of hands-on experience, advanced research models, and deep regulatory understanding. Every program is different, and our work is tailored to the science and objectives behind each one.
Partnering with MedPharm means working with a specialized CDMO built to de-risk development and translate innovation into commercial reality.