Director, Formulation Development

This range is provided by The Steely Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Direct message the job poster from The Steely Group$175,000.00/yr - $250,000.00/yrRecruiting Professional Specializing in Drug Development and Clinical Research.We are seeking an experienced Director of Formulation Developmentto lead and manage a team developing innovative dosage forms and drug delivery systems. Reporting to the Executive Director, Formulation Development, this role will provide strategic and technical leadership across formulation activities while also directing complex projects that are critical to advancing the company’s product pipeline.As an expert in the areas of preformulation and formulation development studies, drug delivery technologies, and product development, this position will be responsible for providing guidance, oversight, and mentoring to a team of scientists. This role will anticipate potential developmental challenges and implement mitigation strategies to reduce program risk.ResponsibilitiesLead and manage a team of scientists in the development and execution of complex formulation projects for injectable small molecules, peptides, and proteins using novel proprietary formulation platforms.Provide strategic direction and guidance to the formulation development team on all aspects of injectable small molecule, peptide, and protein formulations, including process development, characterization, scale-up, tech transfer and manufacturing support.Lead high throughput screening of excipients, selection of primary drug container closure systems, identification of degradation pathways, and development of stable formulations.Lead the development and implementation of novel formulation strategies for injectable products, including long-acting formulations, sustained release formulations, and targeted delivery systems.Demonstrate a thorough understanding of relevant technical/scientific literature, standard procedures, and pharmaceutical regulations relevant to the programs.Develop and implement innovative methods for characterization and stability testing of injectable biologics.Drive the development of robust and scalable manufacturing processes for injectable products.Identify and mitigate technical risks associated with formulation development and manufacturing. Anticipate manufacturability challenges associated with parenteral drug product development.Develop and manage project budgets and timelines, ensuring efficient and on-time completion of projects.Communicate effectively with cross-functional teams (e.g., R&D, Regulatory, Manufacturing) to ensure seamless product development.Provide guidance on quality aspects across regulatory filings related to specifications, acceptance criteria, and stability protocols.Cultivate partnerships by serving as lead point of contact with contract manufacturing organizations and external collaborators.Ensure compliance with all relevant regulatory requirements for injectable products, including ICH guidelines and FDA regulations.Contribute to the preparation and submission of regulatory documentation, including INDs, NDAs, and BLAs.Provide expert technical support during regulatory inspections and auditsli>Build a high performing team through mentoring, goal setting, and supporting the continuing education of junior staff.Contribute to the development of internal training programs and seminars related to formulation science and technology.Write and review study protocols and reports (both formal and informal) to support product development studies and regulatory filings.Stay current with the latest scientific literature and present findings at industry conferences and events.Identify and evaluate emerging technologies and trends in the field of injectable formulation development.Develop and implement strategic initiatives to improve the efficiency and effectiveness of the formulation development process.QualificationsPh.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering or related discipline.A minimum of 10 years in pharmaceutical development, with increasing management responsibility.Familiarity with regulatory requirements for pharmaceutical development.Passion for innovation and scientific discovery, developing junior staff, and advancing healthcare through novel medicines.Knowledge and proficiency using experimental design and statistical analysis software (e.g., JMP / MiniTab / GraphPad Prism).Competencies: Attention to Detail, Independent Judgement, Teamwork & Collaboration, Self-Starter, Adaptability, Professionalism, Written & Verbal Communication skills, Functional Leadership, Problem-Solving skills, Project Management skills. #J-18808-Ljbffr