Senior Scientist Product Development
Listed on 2026-06-20
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Science
Research Scientist, Medical Science
Senior Scientist Product Development 私たちがしていること
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Role reports to: RESEARCH MANAGER
Location:
North America, United States, New Jersey, Summit
勤務地: ハイブリッド
あなたがすることWe are seeking a motivated and experienced Senior Scientist to join Self-Care Product Development team. Reporting directly to a Manager in the Product Development team, this role focuses on supporting the development and optimization of consumer health products, with an emphasis on over-the-counter (OTC) medications and supplements. The Senior Scientist will play a critical role in ensuring product efficacy, safety, and compliance with regulatory standards.
The ideal candidate will have a strong background in formulation science, process development, and experience in GxP (e.g. GDP, GMP, GCP) compliance.
- Lead consumer centric formulation and development of consumer health products, including OTC medications, dietary supplements, and personal care items, ensuring they meet quality and efficacy standards.
- Exercise considerable latitude in determining technical objectives and in selecting techniques and evaluation criteria for obtaining resolution to complex and dynamic problems in consultation with manager.
- Identify and resolve technical challenges in product and process development, utilizing sound scientific principles and experimental data under general guidance.
- Support the optimization of manufacturing processes to enhance efficiency, scalability, and robustness.
- Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project.
- Work closely with cross-functional teams, including R&D, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals.
- Stay up-to-date with the latest scientific advancements and incorporate them into research projects
- Prepare and maintain detailed documentation for product development processes, including experimental protocols, batch records, and technical reports in compliance with Good Documentation Practices (GDP)
Required Qualifications
- Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Engineering, Biomedical Engineering, Biophysics, or a related field.
- Ph.D. in Pharmaceutical Sciences +0-2yr, M.S. with 3+ years of relevant experience, or Bachelor’s Degree with 4+ years of relevant experience.
- Experience in solid dose formulation and manufacturing (tablets).
- Experience in formulation of liquid for ingestion.
- Strong knowledge of formulation science, process development, and foundational understanding of regulatory requirements for OTC medications and dietary supplements.
- Proficiency in analytical techniques and methods used in product development and quality control.
- Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely.
- Ability to work collaboratively within a multidisciplinary team and across various functions.
- Strong analytical and problem‑solving skills.
- Experie…
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