No Relocation Assistance Offered
Job Number #175055 - Piscataway, New Jersey, United States
Responsibilities include:
Lead the development and implementation of new oral care formulas for North America
Be the R&D point of contact for commercial teams for oral care innovation.
Lead experimental designs to help identity launch formulations and production processes.
Make lab and pilot batches of formulations for stability testing and customer sampling.
Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials and batch execution.
Support plant trial batches at various North America locations as needed.
Manage multiple stability studies at the lab, pilot and plant scale, working with support groups (analytical, flavor, micro, etc) to deliver samples and follow up on results.
Create/maintain all required R&D documentation to ensure flawless, high quality commercialization. This may include R&D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, NODs, change control documents and technical justifications.
Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals and influence beyond your network
Create and maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required.
Maintain a clean and organized working environment.
Work on multiple tasks with changing priorities.
Make day-to-day recommendations and escalate issues regarding formula development.
Stay abreast of supplier and competitor’s new developments.
Abide by and follow all company standard operating procedures (SOPs) including those for product development, regulatory and safety.
Deliver effective presentations of technical data and project status.
Required Qualifications
Bachelor’s degree in Chemistry, Chemical Engineering, Biochemistry, Food Science or any other related field.
4+ years of experience in formulation development and technical implementation within a consumer goods environment or 2+ years of experience with a Master’s Degree.
Experience scaling up formulations from the lab through pilot or manufacturing scale.
Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry)
Knowledge of cGMP /GMP and GLP
Preferred Qualifications
Knowledge of equipment and procedures for making oral care formulations
Experience running stability studies for OTC/Drug products
Experience & understanding of producing formulations at the manufacturing scale.
Experience with claim substantiation.
Strong project planning and management experience
Knowledge of Regulatory environment in North America and across the globe.
Knowledge of ICH/FDA guidelines for stability and testing of new drug products.
Able to multi-task and coordinate various simultaneous projects
Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance
Strong oral and written communication skills
Self-motivated but able to work well within a team environment
Excellent computer skills (MS Office, Google suite, SAP, etc.)
Compensation and Benefits
Salary Range $96,800.00 - $137,000.00 USD
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