Product Development Scientist II - Formulation & PoC

Tris Pharma

South Brunswick (NJ)

On-site

USD 90,000 - 115,000

Full time

14 days+

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Benefits offered by this job

Bonus eligible
Medical, dental, vision, Rx insurance
401K with match
Paid time off (PTO)
Volunteer time off

Job summary

Tris Pharma, Inc. invites applications for a Product Development (PD) Research Scientist II in Monmouth Junction, NJ. The role focuses on pre-formulation and formulation activities to develop novel drug delivery platforms, including pilot batch manufacture under cGMP and related documentation.

Interacts with Analytical and Project Management to meet milestones. The candidate should have a Masters with 3–5 years experience or a PhD with 0–2 years experience, with strong technical writing and

Qualifications

  • Hands-on experience in designing and conducting pharmaceutical formulation and process development studies
  • Good understanding of Physical Pharmacy and Pharmaceutics
  • Strong technical writing skills including SOPs, investigations, protocols and reports
  • Familiarity with FDA/OSHA/DEA, cGMPs and GLPs regulations and guidances

Responsibilities

  • Plan and execute pre-formulation and formulation activities to assess feasibility of novel drug delivery platforms
  • Plan, coordinate and execute cGMP pilot batches with appropriate documentation
  • Collaborate with Analytical and Project Management to meet timelines and milestones
  • Prepare technical reports including feasibility reports and invention disclosures
  • Collaborate with QA on investigations, CAPAs and change controls

Skills

Formulation development
Process development
Technical writing
Regulatory knowledge

Education

Masters in Pharmaceutical Sciences
PhD in Pharmaceutical Sciences

Job description

Tris Pharma, Inc. invites applications for a Product Development (PD) Research Scientist II in Monmouth Junction, NJ. The role focuses on pre-formulation and formulation activities to develop novel drug delivery platforms, including pilot batch manufacture under cGMP and related documentation.

Interacts with Analytical and Project Management to meet milestones. The candidate should have a Masters with 3–5 years experience or a PhD with 0–2 years experience, with strong technical writing and

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