Full-Time

Analytical Scientist

MedPharm

MedPharm

Topical and transdermal drug delivery CDMO

No salary listed

Guildford, UK

In Person

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Microsoft Office
Quality Assurance (QA)
Biochemistry
Requirements
  • A Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
  • More than 2 years of relevant industry experience.
  • Familiarity with common analytical equipment and instrumentation, including analytical balances, pH meters, high-performance liquid chromatography, and gas chromatography.
  • Computer literacy and knowledge of Microsoft Office applications.
  • Good observation skills and the ability to document accurately.
  • Good knowledge and practical experience in an analytical laboratory.
  • The ability to work collaboratively in teams.
  • Good time management and organizational skills.
  • The ability to meet the physical demands of occasionally lifting up to 20 kilograms, standing for extended periods, and potential exposure to loud noise and hot or cold temperatures.
Responsibilities
  • Execute analytical techniques such as high-performance liquid chromatography and gas chromatography to support pharmaceutical drug product development and the day-to-day running of the laboratory in compliance with MedPharm's quality management system.
  • Perform and plan predefined experiments according to internal standard operating procedures, including forced degradation of substances and products, saturated solubility, excipient compatibility, and formulation stability studies.
  • Support analytical method development and validation in accordance with International Council for Harmonisation guidelines, including contributions to formal update writing.
  • Document all experiments and results accurately and demonstrate good laboratory practice, data integrity, and quality.
  • Analyze data using Empower and interpret results to support formulation development, stability studies, and product release.
  • Take responsibility for the quality and compliance of analytical work, particularly in support of the analytical team.
  • Drive study progression by collaborating with other departments, attending meetings, and contributing when appropriate under supervisor oversight.
  • Participate in 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 physical and MasterControl-based training file.
  • Follow appropriate health and safety guidance before using equipment or handling chemicals.
  • Undertake general waste disposal and contribute to the tidiness and cleanliness of the laboratory environment.
  • Conduct work in accordance with the MedPharm ethos, professionalism, and confidentiality.
  • Undertake other responsibilities or tasks within the employee's skills and abilities when reasonably requested.

MedPharm is a contract development and manufacturing organization specializing in topical, transdermal, and mucosal drug delivery. It provides end-to-end services from formulation development through clinical and commercial manufacturing, including analytical testing and regulatory support, and operates proprietary delivery platforms such as MedSpray, MedTherm, and AquaRMed. Its capabilities cover dermal, pulmonary, nasal, ophthalmic, and other mucosal routes, combining research services with a patent portfolio to support product lifecycle needs. In 2024 it merged with Tergus Pharma to expand into hormone-based and highly potent drugs, with the goal of helping pharmaceutical and biotech customers move from early formulation to scalable, reliable manufacturing for clinical and commercial use.

Company Size

N/A

Company Stage

Grant

Total Funding

$390K

Headquarters

Guildford, United Kingdom

Founded

1999

Simplify Jobs

Simplify's Take

What believers are saying

  • February 2025 CEO Bill Humphries signals post-merger growth execution and commercial discipline.
  • The Durham $4 million expansion created space for over 100 skilled hires in RTP.
  • Palvella's positive March 2026 Phase 3 readout and Purna partnership strengthen sponsor validation.

What critics are saying

  • MedPharm depends on niche topical spending; a sponsor slowdown hits utilization fast in 2025-2026.
  • The 2024 merger left some Tergus leaders exiting, creating integration and execution risk.
  • Topical CDMO giants and captive pharma plants can compress margins and steal repeat programs.

What makes MedPharm unique

  • MedPharm remains the topical and transepithelial CDMO specialist after the 2024 Tergus merger.
  • Durham and Guildford sites give MedPharm integrated development, clinical manufacturing, and commercial production.
  • August 2026 Olink CSP status adds proprietary proteomics beyond formulation and in vitro testing.

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Company News

FinSMEs
Jul 9th, 2024
MedPharm and Tergus Pharma Merge

MedPharm, a Guildford, UK-based topical and transdermal Contract Development and Manufacturing Organization (CDMO) and Ampersand Capital Partners portfolio company, announced a merger with Tergus Pharma, a Research Triangle Park, NC-based end-to-end contract service provider and a Great Point Partners portfolio company

FinSMEs
Jul 8th, 2024
MedPharm and Tergus Pharma Merge

MedPharm, a UK-based CDMO, has merged with Tergus Pharma, a US-based contract service provider. The combined entity will operate under the MedPharm name, offering end-to-end drug development and manufacturing services. Michael Kane, Tergus Pharma CEO, will become CEO of MedPharm, while Patrick Walsh remains Executive Chairman. Great Point Partners retains a significant minority stake, with Ampersand Capital Partners and Bourne Partners Strategic Capital holding majority ownership.