Sr. Scientist Formulation

Integrated Resources Inc.

Ten Mile Run (NJ)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Job summary

A premier staffing firm is seeking a Formulation Scientist with hands-on experience in developing generic Oral Solid Dosage Forms. The ideal candidate will possess 3 to 5 years of experience in the generic drug industry and work collaboratively to design experiments, analyze data, and communicate project progress effectively. This role offers an opportunity to impact product development significantly.

Qualifications

  • 3 - 5 years of experience in the generic drug industry.
  • Experience in developing oral solid dosage forms from bench scale to large scale.
  • Knowledge of DEA controlled substances and relevant regulations.

Responsibilities

  • Develop generic Oral Solid Dosage Forms.
  • Conduct extensive literature searches on projects.
  • Plan, design, and execute experiments for product development.
  • Analyze data and summarize findings in reports.

Skills

Industrial experience
Ability to perform literature search
Development of non-infringing formulations
Familiarity with QbD elements
Sound knowledge of pharmaceutics
Data analysis and reporting
Team collaboration

Education

Bachelor's or Master's degree in a relevant field

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.

Job Description

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
  • 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.
Qualifications
  • 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
  • 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..
Additional Information

Skilled in Formulation Product Development

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