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MedPharm

Topical and transdermal drug delivery CDMO

Scientist 3 - Analytical R&D

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listedIn-person

About the Job

Requirements

  • A B.S. with 8+ years of experience, an M.S. with 6+ years of experience, or a Ph.D. focused in chemistry, biology, or pharmaceutics.
  • At least 4 years of experience in a GMP laboratory setting.
  • A proven track record developing and validating GMP-compliant HPLC and GC methods to assess drug product stability.
  • Experience diagnosing and troubleshooting HPLC instrumentation and addressing out-of-specification and out-of-trend results.
  • Experience operating HPLC and GC instruments.
  • Knowledge of Empower 3 software.
  • Knowledge of current good manufacturing practice regulations and International Council for Harmonisation, United States Pharmacopeia, and Food and Drug Administration guidelines.
  • Ability to communicate and present information logically and articulately in a manner appropriate for the audience.
  • Ability to perform work conscientiously, attend to detail, and use logical, organized, and methodical thinking.
  • Ability to lift and carry up to 20 pounds occasionally and to stand and walk for extended periods in a climate-controlled laboratory.
  • Ability to perform frequent bending, lifting, pushing, pulling, carrying, and sitting; the role may involve moderate noise in a climate-controlled laboratory.

Responsibilities

  • Develop and validate analytical methods supporting drug formulation development in a GMP-compliant laboratory under minimal supervision.
  • Perform routine testing, including stability testing, solubility studies, and drug-excipient compatibility studies as needed.
  • Independently own projects, including literature review, material sourcing, experimental design and execution, delegating tasks, and providing data to customers.
  • Perform forced degradation studies.
  • Author product development reports and investigation reports.
  • Author or co-author analytical method, validation and transfer, instrument qualification, and validation/qualification protocols and reports, as well as standard operating procedures.
  • Troubleshoot instruments, peer-review laboratory notebooks, and maintain logbooks.
  • Maintain laboratory equipment, including scheduling calibration, acquisition, and basic maintenance programs.
  • Maintain a GMP-compliant analytical laboratory and safe working environment, and maintain laboratory inventory.
  • Review laboratory notebooks, data packages, and reports under minimal supervision, and trend stability data.
  • Present data to customers and attend client meetings as needed under minimal guidance.
  • Supervise, mentor, train, and develop junior scientists; there are no direct reports and there are indirect reports.
  • Collaborate with Process Development/Formulation R&D, Quality Control, and Quality Assurance.

Desired Qualifications

  • Experience developing methods for topical drug products.
  • Experience with ultraviolet spectroscopy, Fourier-transform infrared spectroscopy, Karl Fischer titration, optical microscopy, particle size distribution, viscosity, and rheological methods.
  • Technical report writing proficiency.
  • Experience with MasterControl and Microsoft Office.

About the Company

MedPharm

Topical and transdermal drug delivery CDMO

MedPharm is a contract development and manufacturing organization focused on 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 to enable multiple administration routes. The company combines contract research with a patent portfolio and offers lifecycle support across development and manufacturing, differentiating itself from competitors. A July 2024 merger with Tergus Pharma expanded capabilities to include hormone-based and highly potent drugs, enhancing scale and scope with the aim of helping pharma and biotech move products from early formulation to scalable manufacturing.

Company size
Not listed
Company stage
Grant
Total funding
$390K
Headquarters
Guildford, United Kingdom
Founded
1999

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