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Senior Scientist, Formulation Science

Job in Durham, Durham County, North Carolina, 27701, USA
Listing for: Implaion Recruiting
Full Time position
Listed on 2026-08-20
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing, Pharma Engineer, Drug Discovery
  • Research/Development
    Pharmaceutical Science/ Research, Drug Discovery
Job Description & How to Apply Below

Senior Scientist in Formulation Sciences

This is a drug delivery role inside the Formulation Sciences team. You'd own selection and advancement of the delivery system — prefilled syringe, autoinjector, or on-body — for a self-administered protein biologic. Device and combination product experience is the requirement. Hands-on selecting and advancing a delivery system for a biologic, plus the regulatory work to take it into the clinic. We'll coach the formulation side.

Strong device background with lighter formulation depth is a trade we'll make. Formulation development alone isn't a fit, and neither is device design engineering — we select and qualify systems, we don't build them.

About the Position

As a Senior Scientist in Formulation Sciences, you will be an integral part of the formulation sciences team. This team is responsible for developing formulations for the clinical and commercial manufacturing of therapies. The position is also responsible for partnering with external companies to advance devices for self-administered delivery of our therapeutics to patients. The position will help interface with CDMOs specializing in drug product manufacturing operations to manufacture our drug in both vial and device form for delivery to clinical sites and eventually patients worldwide.

This full-time, regular position will be located onsite in Durham, NC. The level and remuneration will be commiserate with experience.

Summary of Key Responsibilities

  • Lead pre-formulation and formulation development activities for drug substance and drug product, including excipient screening, formulation optimization, and assessment of product quality attributes
  • Interface with external companies to screen, identify, qualify, manufacture and supply appropriate pre-filled syringe (PFS) systems, auto-injectors and on body drug delivery systems as appropriate
  • Design stability and forced degradation studies, author protocols, oversee execution at internal or external laboratories, and review data generated by third-party vendors
  • Develop and apply biophysical and analytical methods to characterize formulation performance, including assessments of aggregation, thermal stability, viscosity, particulate risk, and protein higher-order structure
  • Analyze samples and data, interpret results, and author or review technical reports that support formulation selection, process transfer, manufacturing readiness, and regulatory submissions
  • Identify and implement technologies that improve formulation development workflows, and support transfer of formulation and drug product processes into pilot plant, CDMO, and cGMP manufacturing environments
  • Evaluate container closure systems and delivery technologies for biologic drug products, including prefilled syringes, on-body delivery systems, syringe ability, injectability, viscosity, dose compatibility, and particulate characterization
  • Generate internal and external technical documents that support manufacturing, development decisions, and CMC sections of regulatory filings
  • Lead or support drug product fill-finish development, scale-up, and transfer activities, as appropriate for program needs
  • Routine interaction with Analytical Development, Downstream Process Development, Pilot Plant, Clinical, Research, Quality, Regulatory, and external partners will be essential to success in this role.
  • The successful candidate will help train and mentor colleagues in formulation development, sample analysis, data interpretation, and GxP laboratory practices.
  • Development of liquid formulations for protein-based therapeutics (including high concentration development)
  • Collaboration with drug product CDMOs

Required Qualifications

  • Ph.D. in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, Biological Sciences, or a related discipline with at least 1-3 years of formulation development experience in the pharmaceutical or biotechnology industry, preferably with biopharmaceutical products, or, B.S. or M.S. in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, Biological Sciences, or a related discipline with at least 5-8 years of formulation development experience in the…
Position Requirements
10+ Years work experience
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