Formulations Scientist – Tablet & Liquid Medicine focus, 401k

🏢 Pfizer📍 Oklahoma City, OK, United States💼 Full-Time💻 On-site🏭 Pharmaceuticals💰 85000-130000 per year

About the Company

Pfizer is a global biopharmaceutical company dedicated to the discovery, development, manufacture, and commercialization of healthcare products. With a commitment to innovation and patient well-being, we strive to bring therapies to people that significantly improve their lives. Our diverse portfolio covers a wide range of therapeutic areas, and we are constantly pushing the boundaries of science to address unmet medical needs worldwide. Join our team and contribute to a healthier world.

Job Description

We are seeking a highly motivated and experienced Formulations Scientist to join our dynamic R&D team in Oklahoma City. This role will focus on the development of novel tablet and liquid medicine formulations, from early-stage development through to commercialization. The ideal candidate will possess a strong background in pharmaceutical science, a deep understanding of formulation principles, and hands-on experience with various dosage forms. You will play a critical role in designing, executing, and interpreting experiments to develop robust and stable drug products, ensuring compliance with regulatory standards.

Key Responsibilities

  • Design and execute formulation development studies for oral solid dosage forms (tablets) and liquid formulations, including solutions, suspensions, and emulsions.
  • Conduct pre-formulation studies to characterize drug substance properties and guide formulation strategies.
  • Develop and optimize manufacturing processes for new formulations at lab, pilot, and potentially commercial scales.
  • Perform stability studies and analyze data to assess product shelf-life and support regulatory submissions.
  • Collaborate cross-functionally with analytical, process development, and clinical teams.
  • Author and review technical reports, protocols, and regulatory documents.
  • Stay current with scientific literature, industry trends, and new technologies in pharmaceutical formulation.
  • Ensure all work is performed in compliance with cGMP, ICH guidelines, and company SOPs.

Required Skills

  • PhD or Master's degree in Pharmaceutical Sciences, Chemical Engineering, or related field with 3+ years of relevant industry experience.
  • Proven experience in developing tablet and liquid formulations.
  • Strong understanding of pharmaceutical excipient properties and their impact on drug product performance.
  • Proficiency in experimental design (DoE) and statistical data analysis.
  • Hands-on experience with pharmaceutical processing equipment (e.g., tablet presses, blenders, granulators, high-shear mixers).
  • Knowledge of cGMP principles and regulatory requirements for pharmaceutical development.
  • Excellent problem-solving, analytical, and communication skills.

Preferred Qualifications

  • Experience with advanced drug delivery systems.
  • Familiarity with Quality by Design (QbD) principles.
  • Experience working with contract manufacturing organizations (CMOs).
  • Publications in peer-reviewed journals related to pharmaceutical formulations.

Perks & Benefits

  • Comprehensive health, dental, and vision insurance.
  • 401k retirement plan with company match.
  • Generous paid time off and holidays.
  • Life and disability insurance.
  • Employee assistance program.
  • Tuition reimbursement and professional development opportunities.
  • On-site fitness center and wellness programs.

How to Apply

If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:

  • An up-to-date Resume or CV
  • A brief cover letter summarizing your experience and motivation

Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.

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