Scientist -I

Job description

Scope A Scientist-Contractor will be responsible for technical support to the Neutrogena manufacturing facility and general marketed product support for cosmetic, personal care and OTC monograph drug products . This individual will work, under supervision, in a team environment with Operations, Supply Chain, Quality Assurance, Product Development, Technical Transfer, Analytical Development, Microbiology, Regulatory and Marketing Personnel.. Responsibilities. Technical service support to activities related to continuous LAP manufacturing facility improvement such as execute studies to support product bulk hold time; execute raw material stability and compatibility studies. • Work collaboratively across functional groups in accomplishing the studies and implement the changes. • Conduct NC/CAPA investigations, Action Plans, and Verification/Validation Activities, root cause determination 4. Qualifications • B.S. or M.S. in Chemical Engineering, Materials/Polymer Science, Chemistry or other science discipline, 3 years professional experience; or M.S. with 0-3 years of professional experience. • Extensive knowledge of Emulsion theory, design, and processing • Experience with beauty products and emulsion processes • Understanding of cGMPs and current FDA Compliance requirements is must • Experience in developing semi-solid products or process development • A technical knowledge base of physical chemistry, chemistry and material sciences. • Experience with formulated products including emulsions, surfactants, toothpastes, suspensions, etc. • Problem Solving: Proactively seek solutions; Gather and analyze information systematically; Develop alternative solutions; Think analytically and act decisively. • Master Complexity: Competently handle day-to-day work challenges; Thrive in uncertain circumstances; Detail oriented and ability to work collaboratively across functional groups and handle multiple responsibilities and projects. • Communication: Excellent oral and written communication skills. Write clearly and informatively; Create documents that are complete and accurate. • Commitment: Strive to attain quality results on time; convey a sense of urgency and drive issues to closure; earn a reputation for reliability and dependability. • Strong technical writing skills • Understanding of compliance both from quality and regulatory standpoint • Be able to work effectively cross functionally and accurately communicate risks and requirements. • The ability to work independently and to meet timeline schedules. • Requires strong technical and communication skills • Computer literacy and full understanding of Microsoft Office 5. Can be acquired on job: • Site specific software required by client • SOP’s and Work Instructions developed by client Contact me at 732 429 1850 if interested A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client