Scientist Jobs

About The Position

Requirements

• PhD in Pharmaceutical Sciences, Chemical Engineering, Materials Science, Polymer Science, Chemistry, Biochemistry, or a related scientific discipline.
• 0–4+ years of relevant pharmaceutical, biotechnology, medical device, or combination product development experience, including substantial experience in drug delivery and formulation development.
• Demonstrated expertise in sustained-release or controlled-release drug delivery technologies.
• Experience leading formulation and process development from early feasibility through scale-up and technology transfer.
• Strong working knowledge of polymer science, material characterization, drug-release testing, stability assessment, and pharmaceutical development principles.
• Ability to independently design experiments, analyze complex data, draw scientifically sound conclusions, and recommend next steps.
• Excellent technical writing, presentation, collaboration, and problem-solving skills.

Nice To Haves

• PhD in a related scientific discipline with 4+ years of experience.
• Hands-on industrial experience with hot melt extrusion, injection molding, and hydrogel processing, including formulation development, equipment selection, process optimization, scale-up, and troubleshooting.
• Experience developing ophthalmic drug products, long-acting delivery systems, implants, inserts, or combination products.
• Experience with polymer-based drug delivery systems and characterization of solid dispersions or extrudates.
• Knowledge of cGMP manufacturing, process validation, and technology transfer requirements.
• Experience supporting IND, IMPD, NDA, or other global regulatory submissions.
• Track record of publications or significant scientific contributions in drug delivery.

Responsibilities

• Lead the design, development, and optimization of novel drug delivery systems, including sustained-release and controlled-release dosage forms.
• Develop targeted and sustained formulations using polymeric matrices, implants, microparticles, nanoparticles, hydrogels, and other advanced delivery technologies.
• Design and execute studies to characterize drug release kinetics, formulation stability, material properties, and product performance.
• Evaluate structure-property relationships affecting drug loading, release behavior, stability, manufacturability, and product quality.
• Select and characterize excipients, polymers, active pharmaceutical ingredients, and other critical raw materials.
• Develop robust, scalable formulation and manufacturing processes for preclinical, clinical, and commercial supply.
• Apply Quality by Design and Design of Experiments principles to identify critical material attributes, process parameters, and quality attributes.
• Lead technical troubleshooting and root-cause investigations for formulation, process, and product-performance challenges.
• Support scale-up, technology transfer, process characterization, and validation with internal teams and external manufacturing partners.
• Provide technical leadership for hot melt extrusion process development and optimization when applicable.
• Provide scientific and technical leadership across drug delivery programs and influence platform strategy, development priorities, and project decisions.
• Serve as a subject matter expert in sustained-release technologies, formulation science, and pharmaceutical drug delivery.
• Identify technical risks, recommend mitigation strategies, and communicate development options to cross-functional teams and leadership.
• Evaluate emerging technologies and translate relevant scientific advances into practical development strategies.
• Contribute to invention disclosures, patent applications, publications, and other intellectual-property activities.
• Partner with CMC, Analytical Development, Nonclinical, Clinical Development, Regulatory Affairs, Quality, Engineering, and Manufacturing to align technical plans with program objectives.
• Author and review protocols, technical reports, development summaries, presentations, and CMC sections of regulatory submissions.
• Support responses to health authority questions related to formulation, process development, characterization, and product performance.
• Manage technical interactions with consultants, contract research organizations, contract development and manufacturing organizations, and other external partners.
• Mentor junior scientists and research associates in experimental design, data interpretation, documentation, and scientific communication.
• Maintain complete, accurate, and timely laboratory records and development documentation.
• Ensure activities comply with applicable quality systems, cGMP expectations, safety requirements, and internal procedures.