MSAT Scientist II - 249708

MSAT Scientist

II - 249708

at Medix MSAT Scientist

II - 249708

at Medix in Brielle, New Jersey Posted in 2 days ago.

Type:

full-time

Job Description:

This role supports Manufacturing Science & Technology (MS&T) activities for pharmaceutical products across development and commercialization, with a focus on parenteral and nasal dosage forms. The position contributes to scale-up, process optimization, technical documentation, and cross-functional collaboration while ensuring compliance with regulatory, quality, and safety requirements. The ideal candidate is technically strong, detail-oriented, and comfortable supporting projects in a fast-paced, regulated manufacturing environment.

Responsibilities:

Execute Manufacturing Science & Technology (MS&T) activities with minimal supervision for pharmaceutical products, including parenteral and nasal dosage forms, supporting new products from scale-up through commercialization and ongoing post-commercialization process improvements. Develop a growing understanding of generic and novel drug development processes, regulatory agency requirements, and CMC strategies. Adhere to all company safety, environmental, quality, and compliance practices in accordance with departmental guidelines, SOPs, and applicable federal, state, and local regulations; ensure departmental SOPs are established and consistently followed. Support project execution under supervision by tracking action items, meeting timelines, and providing accurate technical information to cross-functional support teams. Build and maintain effective working relationships with cross-functional partners, external customers, and stakeholders; may serve as a scientific contributor on client calls related to MS&T activities. Prepare project protocols and define deliverables with limited supervision; review and evaluate technical data, documentation, and proposals. Provide technical support and guidance for both development-stage and commercial products through technical communications, reports, and memoranda. Learn to trend and analyze process data to ensure specifications are met, including performing Process Capability Analysis. Ensure batch records are clear, accurate, and operationally executable; support training of Operations personnel to ensure confidence in commercial manufacturing processes. Support assigned regulatory inspections and audits. Work effectively in a collaborative, team-oriented environment. Comply with all company policies and maintain flexibility in work schedule based on business needs. Perform additional duties as assigned.

Qualifications:

Bachelor's degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering, or a related discipline, with 3-5 years of relevant experience in MS&T or Product Development; or Master's degree in Pharmaceutical Sciences, Formulation Chemistry, Chemical Engineering, or a related discipline, with 1-3 years of relevant experience in MS&T or Product Development. PhD in Pharmaceutical Sciences or Formulation Chemistry is a plus.