Expoint – all jobs in one place
The point where experts and best companies meet
Limitless High-tech career opportunities - Expoint

Teva Principal Product Development Scientist 
United States, Florida, Weston 
576275060

26.08.2025
How you’ll spend your day
  • Design and develop oral solid dosage forms (immediate and extended release) from concept through regulatory submission and product launch.
  • Develop and execute formulation strategies, including project planning, experimental design, data analysis, and coordination with cross-functional teams (Analytical Sciences, Legal & Regulatory, Pharma Tech).
  • Maintain expertise in controlled release technologies and contribute to innovation in drug delivery systems.
  • Identify and implement improvements in R&D processes, technologies, and regulatory compliance.
  • Conduct pre-formulation and formulation development work; generate and review analytical data to support product development.
  • Author protocols, batch records, and documentation for scale-up and pivotal batch manufacturing.
  • Plan and oversee analytical testing and stability studies for pivotal batches.
  • Prepare comprehensive documentation including Product Development Reports (PDR), Quality Overall Summaries (QOS), and other regulatory filing materials.
  • Conduct literature reviews and patent searches to stay current with industry trends and regulatory changes.
  • Plan and evaluate bioequivalence studies; recommend formulation changes based on data.
  • Ensure compliance with cGMP, cGLP, SOPs, FDA, and DEA regulations.
  • Provide scientific and technical guidance to junior staff to meet project goals and timelines.
  • Collaborate with supervisor to set priorities and achieve objectives.
Your experience and qualifications
  • Master’s degree (or foreign equivalent) in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field, plus 6 years of relevant experience.
    OR
    Bachelor’s degree with 8 years of progressive experience in lieu of the above.
  • Minimum 3 years of experience in:
    • Oral solid dosage formulation development
    • Immediate and extended release dosage forms
    • Process development
    • NDA/ANDA submissions
  • Strong understanding of regulatory requirements and pharmaceutical development processes.
  • Excellent documentation and communication skills.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Innovative product development experience is preferred.

TRAVEL REQUIREMENTS: Up to 10%

We offer a competitive benefits package, including:

Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.

Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.

The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.