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Associate Principal Scientist, Vaccine Drug Product Development

Job in West Point, Montgomery County, Pennsylvania, 19486, USA
Listing for: MSD Malaysia
Full Time position
Listed on 2026-07-26
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 142400 - 224100 USD Yearly USD 142400.00 224100.00 YEAR
Job Description & How to Apply Below
Location: West Point

Primary Responsibilities

Design, execution, and documentation of experiments to develop stable formulations and robust manufacturing processes for preclinical and clinical supply production and to scale-up these processes to the pilot plant and commercial space. The successful candidate will be expected to work independently in a hands-on, dynamic laboratory environment engaged in development activities while also working collaboratively within the group, across functional areas, and with external partners.

Active strategic and technical leadership on program development teams will be required. Strong communication skills are expected to clearly communicate data and conclusions verbally, through written documents and reports, and technical presentations. Proven facilitative leadership and communication skills are essential to effectively support matrix teams and manage expectations of stakeholders as part of our stage-gate process used to manage the development of new products.

The role will also entail supporting or leading teams to advance areas such as science and technology innovation, business process improvement, and clinical manufacturing capability build. Successful candidates are motivated to excel, willing to take initiative, have a strong desire to learn and contribute, and actively mentor less experienced scientists. Successful candidates will have a track record of external publication, patenting, and presentations.

Required

Experience and Skills
  • Ph.D. in chemical/biochemical engineering, pharmaceutical sciences, chemistry, biochemistry, or related discipline with minimum of 6 years of relevant industrial experience; an M.S. degree in a similar field with minimum of 8 years of relevant industrial experience; or a B.S. degree in a similar field with minimum of 10 years of relevant industrial experience
  • Proven written and verbal communication skills
  • Ability to prioritize, plan, and execute work with limited guidance
  • Ability to work in a dynamic and fast-paced team environment
  • Demonstrated facilitative leadership and influencing skills
  • Hands‑on laboratory skills
  • Experience developing vaccine adjuvant, vaccine drug product, and/or biologics drug product processes including advanced knowledge of key unit operations (freeze/thaw, formulation, mixing, filtration, filling, stoppering, etc.)
  • Understanding of sterile drug product quality attributes, specifications, characterization techniques, and product vulnerabilities and mitigation strategies
  • Track record of difficult technical problem solving
  • Ability to develop and implement new methods/processes
  • Experience with use of statistical principles to understand, predict, and communicate process robustness
  • Experience with root cause analysis and investigations (FMEA, fishbone, etc.)
  • Experience, desire, and a track record of effective mentorship of less experienced scientists towards timebound goals
Desired Experience and Skills
  • Experience with sterile product manufacturing and aseptic technique, and experience with GMP manufacturing of clinical supplies
  • Experience with technical transfer of processes from lab to pilot plant and/or commercial sites including the use of risk assessment tools
  • Experience with engineering principles used in process development and process scale up/scale down
  • Experience with colloidal systems and characterization of colloids including emulsions
  • Familiar with ISO, CFR, ICH, and USP guidelines as they relate to sterile products
  • Familiar with Quality by Design principles and have experience applying the Quality by Design tools and principles to products in development
  • Experience with liquid and lyophilized drug product formulation development
  • Experience authoring regulatory filings for sterile dosage forms (adjuvants and/or DP), and experience responding to regulatory questions related to drug products
Required Skills
  • Biochemistry
  • Cell Line Development
  • Detail‑Oriented
  • Downstream Process Development
  • Drug Delivery Technology
  • Drug Development
  • Expression Vectors
  • Facilitative Leadership
  • GMP Compliance
  • Interpersonal Relationships
  • Leading Project Teams
  • Mentorship
  • Molecular Biology
  • New Product Development
  • Pharmaceutical Formulations
  • Pharmaceutical Process…
Position Requirements
10+ Years work experience
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