Description
Key ResponsibilitiesFormulation Development: - Design, execute, optimize formulation strategies for biologics (ie. mAbs, LNPs, VLPs, peptides & vaccines all modalities).- Participate in the assessment of new novel polymers. - Design and optimize formulations for biologics using polymers, surfactants, sugars, and novel excipients across multiple modalities. - Develop a formulation strategy/approach that can be utilized by the research team. Stability Testing: - Plan and execute accelerated and real-time stability studies under ICH and stress conditions.Analytical Oversight: - Interpret analytical data (e.g., DLS, titer assays, particle sizing, degradation profiles) to evaluate formulation performance.Technical Execution: - Conduct hands-on formulation and screening work at the bench with team members supporting the formulation development programs.Leadership and collaboration: - Serve as the principal technical lead to tackle challenges associated with stabilization of biologics and exploring alternatives routes of administration.- Foster a collaborative environment through sharing insights and demonstrations of learning and best practices.Requirements:- Ph.D. with 5+ years or M.S. with 8+ years of industry experience in formulation development.- Extensive experience in novel formulation development for a diverse range of large molecule APIs, including viral vectors and bacterial vaccines, as well as mRNA lipid nanoparticle (LNP) formulations, peptides, proteins and mAbs.- Proven industry experience in the development of vaccines and/or other biotherapeutics.
Skills
Formulation, Chemistry, Laboratory, Research & development, biologics, stability testing, analytical assays, leadership
Top Skills Details
Formulation,Chemistry,Laboratory,Research & development,biologics,stability testing,analytical assays,leadership
Additional Skills & Qualifications
Preferred Qualifications:- Expertise in alternative formulation manufacturing techniques, such as lyophilization, films and spray drying. - Experience working with brush polymers. - Experience in small molecule formulation is beneficial but not required.- Proven track record of managing R&D programs. - Strong understanding of regulatory requirements.- Excellent communication, leadership, and documentation skills.- Strong analytical and problem-solving abilities.
Experience Level
Intermediate Level Pay and Benefits The pay range for this position is $105000.00 - $120000.00/yr.- Jurata offers a comprehensive employee benefits package- A discretionary annual bonus program
- Stock-based long-term incentives Workplace Type This is a fully onsite position in Chapel Hill,NC. Application Deadline This position is anticipated to close on Jul 24, 2025. About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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