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Pfizer, S.A. de C.V

Senior Scientist, Molecular Pharmaceutics, Drug Product Design

Pfizer, S.A. de C.V, California, Missouri, United States, 65018


Senior Scientist, Molecular Pharmaceutics, Drug Product Design

Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. Research and Development is at the heart of fulfilling Pfizer’s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.POSITION SUMMARYAs a Senior Scientist in the Molecular Pharmaceutics group, you will act as a resident pharmaceutical science subject matter expert to influence small molecule early drug candidate selection with respect to drug delivery, bio-performance, and stability. This position will closely collaborate with colleagues across PharmSci as well as with partners in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology. You will be responsible for designing, implementing, and interpreting

in vitro, in silico , and

in vivo

experiments, as well as design of stage appropriate traditional and enabled formulations for preclinical studies. This role will also specialize in formulation and characterization of spray dried dispersions (SDDs). An understanding of drug product development, as well as an understanding of the disease state, drug targets and drug-target mechanisms of action, will help to enable and narrow the definition of the required design elements. In additional to formulation, you will be responsible for material science and physicochemical properties assessments of early drug candidates. This includes laboratory measurements and interpretation of the data to inform manufacturing, bio-performance, and stability development risks.KEY RESPONSIBILITIESEvaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment.Design and develop fit for purpose and diagnostic traditional and enabled formulations for preclinical studies.Become a subject matter expert in formulation and process development for SDDs supporting multiple discovery teams across several research units.Design, execute, and interpret the results of polymorph and salt screens for potential drug candidates related to stability, manufacturability, and bio-performance.Apply first principles understanding of thermodynamics and kinetic processes to dissolution and precipitation of drugs in biorelevant conditions and physical and chemical stability in the solid state.Work in cross-disciplinary teams and partner with subject matter experts in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology departments to influence candidate selection and progression. Develop strategic collaborations with academic and industrial researchers for addressing gaps in fundamental or applied science related to the pharmaceutical sciences.Conduct novel research and present significant findings via internal and external presentations or publications.MINIMUM QUALIFICATIONSRecent PhD with 1-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience in Chemical Engineering, Physical Chemistry, Biophysical Chemistry, Biophysics, Physics, Physical Organic Chemistry, Pharmaceutics, Pharmaceutical Sciences or Biochemistry.Candidates with experience in allied disciplines may also apply with the following qualifications: Ph.D. with minimum 3 years, MS with 7+ years, or BS with 12+ years of experience in industry.Experience working independently and collaboratively in a laboratory environment.PREFERRED QUALIFICATIONSExperience in formulation and manufacturing of SDDs targeted at bioavailability enhancement.Experience in breaking down and isolating the controlling physics of complex processes for experimental design.Experience in designing and conducting hypothesis driven laboratory experiments.Generating, interpreting, and integrating experimental data into mathematical models to progress the understanding of complex materials and processes.Experience in pharmacokinetic modeling and simulations using Gastroplus or similar modeling software.Experience with formulation design for preclinical studies as well as awareness of drug product design criteria for phase 1 clinical trials.Strong organizational skills, interpersonal skills, teamwork skills, strong written and verbal communication skills.Ability to prioritize and manage multiple projects and activities while managing tight timelines.PHYSICAL/MENTAL REQUIREMENTSIncludes activities in both laboratory and office settings which would require varying degrees of sitting, standing, moving about the workspace, light lifting, working at a computer, and performing routine laboratory tests and procedures. Also requires the ability to perform mathematical calculations and complex data analysis.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTSOccasional travel may be requested. Laboratory work requires adherence to safe work practices and procedures such as use of Personal Protective Equipment (gowning, gloves, protective eyewear, etc).WORK LOCATIONOn Premise, with relocation support available as needed.

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