Senior Scientist

5 days ago


Philadelphia, United States EPM Scientific Full time

Scientist/ Sr. Scientist- Drug Product Development

Salary: 130K-150K + benefits + bonus

Location: Greater Philadelphia area


A biotech organization local to the east coast specializes in the development of advanced pharmaceutical products. Their team is dedicated to conducting research and creating innovative solutions to address a wide range of health issues. They are committed to upholding the highest standards of quality and ethics in our work, with a focus on improving patient outcomes and advancing the field of healthcare. This organization is seeking a Scientist/ Senior Scientist of Drug Product Development to join their team due to their promising pipeline and progressive programs they are working on.


Responsibilities:

  • Lead and manage the development of biologic drug products from concept to commercialization.
  • Design and execute experiments to optimize formulation and manufacturing processes.
  • Analyze data and interpret results to support decision-making.
  • Conduct stability studies and develop analytical methods for Drug Products with a focus on traditional biologics.
  • Ensure compliance with regulatory requirements throughout the development process.
  • Collaborate with cross-functional teams to drive innovation and success.
  • Communicate findings effectively to internal and external stakeholders.
  • Stay current with industry trends and advancements in drug product development- primarily involving mAbs and ADCs.


Qualifications

  • PhD in Pharmaceutical Sciences with 5 years of industry experience- specifically Drug Product Development.
  • Extensive experience in drug product development, particularly with monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs).
  • Proficiency in designing and executing experiments to optimize formulation and manufacturing processes for traditional biologics.
  • Strong understanding of analytical methods and characterization techniques such as HPLC and UPLC
  • Knowledge of regulatory requirements and experience in ensuring compliance.
  • Proven track record of successful project management and leadership in a cross-functional team environment.
  • Excellent communication skills and ability to effectively collaborate with internal and external stakeholders.
  • Demonstrated ability to stay current with industry trends and contribute to the advancement of biologics drug development.


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