Assoc Principal Scientist, Vaccine Drug Product Development Full-time NEW

Associate Principal Scientist

Vaccine Drug Product Development, a part of our company's Research Laboratories, is seeking an Associate Principal Scientist to join our department in West Point, PA. Our mission is to develop novel vaccine drug products that will profoundly improve global human health—directly building from our company's 50+ year legacy as pioneers in the discovery, development, and manufacturing of novel vaccines to eliminate disease. Our department is responsible for developing vaccine adjuvants and drug products from preclinical studies through Phase III clinical trials with line of sight to commercialization. We ensure robust composition, primary packaging, and process development through deep fundamental understanding and characterization such that the process is scalable without compromising safety, efficacy, or stability. During development, we leverage smart experimental design, cutting edge analytical tools, and statistical/predictive approaches to inform formulation and process development. Our team enables the translation of vaccine preclinical candidates from concepts into robust commercial drug products.

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 and/or vaccine drug product processes, or significant nucleic acid and lipid nanoparticle experience, including advanced knowledge of key unit operations (freeze/thaw, formulation, mixing, filtration, filling, stoppering, etc.)
• Understanding of vaccine adjuvant and/or 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: Accountability, Biochemistry, Biopharmaceuticals, Cell Line Development, Chemical Engineering, Detail-Oriented, Downstream Process Development, Drug Delivery Technology, Drug Development, Expression Vectors, Facilitative Leadership, Global Health, GMP Compliance, Immunochemistry, Interpersonal Relationships, Leading Project Teams, Manufacturing Processes, Mentorship, Molecular Biology, Pharmaceutical Formulations, Pharmaceutical Process Development, Pharmaceutical Sciences, Physical Characterization, Phytochemistry

Preferred 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

Salary Range: $142,400.00 – $224,100.00

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.