Sr. Scientist Formulation

IntegratedResourcesINC

South Brunswick Township, NJ, United States permanent

Posted: January 20, 2016

Job Description

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 a Formulation Scientist role in Generic Pharma. This role is very hands-on

• Formulator with previous industrial experience developing generic Oral Solid Dosage Forms (including Oral Liquids preferred)

• Ability to perform extensive Literature Search on assigned Projects

• Ability to develop non-infringing formulations

• Familiar with adapting QbD elements in generic product development

• Experience working with projects from bench-top stage to large scale manufacture of submission batches

• Should have a sound knowledge of pharmaceutics, pharmacokinetics and process scale-up

• Plan, design and execute experiments for product development

• Analyze data and summarize in form of reports

• Review literature, reports, protocols etc.

• Discuss, prioritize and plan work with external functions such as ARD, TS & Manufacturing

• Provide feedback to senior management on project progress

• Suggest improvements and efficiencies in the department

• Assist in revising and maintaining SOPs, operating procedures and other documents. Suggest new equipment and or training for personnel.

• Formulation and process development scientist with 3 - 5 years of experience in the generic drug industry

• Must have ability to work in a team with excellent spoken and written communication skills

• MS or PhD in Pharmaceutics

• Must have experience in developing oral solid dosage forms from Bench Scale all the way to large scale submission batch manufacture, at other generic Pharma companies

• Experience in working with DEA controlled drug substances and relevant regulations..

Skilled in Formulation Product Development

Generic Drug

ANDA submissions

Generic Drug Development

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