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Health Care 🏢 Full Time ⭐️ Verified

Senior Pharmaceutical Scientist

BioPharm Innovations
Cambridge
Salary Estimate
USD 140.000 – USD 180.000
Live Update
10 Mei 2026
Deadline
10 Mei 2027

Job Description

Join BioPharm Innovations, a trailblazer in biopharmaceutical research, as we pioneer next-generation therapies for unmet medical needs. We're seeking a dedicated Senior Pharmaceutical Scientist to drive innovation in drug development and contribute to life-changing breakthroughs. Our Cambridge-based R&D hub offers cutting-edge facilities and collaborative teams focused on advancing precision medicine and therapeutic innovation. If you're passionate about translating scientific discoveries into tangible health solutions, this is your opportunity to make a global impact.

Responsibilities

  • Lead design and execution of complex preclinical drug development studies, including formulation optimization and stability testing
  • Collaborate with cross-functional teams (chemistry, biology, regulatory) to advance drug candidates from discovery to IND submission
  • Develop and validate analytical methods for characterizing pharmaceutical compounds using HPLC, LC-MS, and spectroscopy
  • Author comprehensive technical documentation including study protocols, reports, and regulatory submissions
  • Mentor junior scientists and maintain compliance with GMP/GLP standards and FDA/EMA regulations
  • Present research findings at scientific conferences and publish in peer-reviewed journals

Qualifications

  • PhD in Pharmaceutical Sciences, Chemistry, or related field with 5+ years industry experience
  • Expertise in small molecule drug development and biopharmaceutical characterization techniques
  • Proven track record in IND-enabling studies and regulatory documentation
  • Strong proficiency with analytical instrumentation (HPLC, LC-MS, NMR) and data analysis software
  • Demonstrated experience in CMC (Chemistry, Manufacturing, Controls) development
  • Excellent project management skills with ability to manage multiple complex timelines
  • Knowledge of ICH guidelines and global regulatory requirements

Required Skills

Drug Development Analytical Chemistry Regulatory Affairs Preclinical Studies HPLC LC-MS GMP/GLP CMC Development

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