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Principal Pharmaceutical Scientist

Job in Maple Grove, Hennepin County, Minnesota, 55311, USA
Listing for: Boston Scientific Gruppe
Full Time position
Listed on 2026-01-08
Job specializations:
  • Engineering
    Biomedical Engineer, Research Scientist
Job Description & How to Apply Below

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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit
- High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

About the role:

This Principal Pharmaceutical Scientist is responsible for design and optimization formulation of drug delivery systems to support combination product development, preclinical and clinical studies. This position is also responsible for characterizing physicochemical properties such as physical form, solubility, stability, and interaction of drug molecules with excipients. This includes experimental planning, design, data analysis and interpretation.

At Boston Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions. We continue to innovate in key areas and are extending our innovations into new geographies and high-growth adjacency markets. As part of R&D team, we design, develop, and produce technologies for diagnosing and treating coronary artery disease and other cardiovascular disorders. Medical Conditions we provide solutions that encompass Coronary Artery Disease, Peripheral Artery Disease, Heart Failure, and other Cardiovascular Diseases.

We are able to provide a number of solutions to patients that include:
Drug-Eluting Stents, Bare-Metal Stents, Catheters, Balloons, Guide Wires, Coronary Atherectomy and Coronary Intravascular Ultrasound. BSC has robust product portfolio and pipeline and will continue to make investment in Interventional treatments to improve the quality of patient’s life.

Work Mode:

This position will follow an onsite schedule, requiring 5 days in-office per week from our Maple Grove site.

Visa Sponsorship:

Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time

Key Responsibilities
  • Selects techniques to solve complex problems and makes sound design recommendations.
  • Solid understanding on controlled drug release mechanism.
  • Drug release and stability testing at internal and external laboratories
  • Write CMC sections to support IDE and PMA submissions for combination products
  • Participate in cross-functional product development teams and provide technical leadership to formulation development, test methods, sterilization process selection, packaging specification requirements, clinical manufacturing, quality assurance, analytical R&D, and regulatory affairs
  • Consistently generates innovative and unique solutions to market needs and submits idea disclosures. Work is expected to result in the development of new or refined products, processes, or equipment.
  • The selected candidate must have an ability to collaborate effectively with other scientists in a multidisciplinary team environment and possess excellent verbal and written communication skills.
  • Ability to research literature and develop clinical understanding with technical credibility to develop a strategy for regulatory submission.
  • Demonstrated ability to provide technical leadership on a large-scale development program.
  • Providing technical direction to technicians/entry-level engineers, mentor junior level engineer
  • Actively collaborating with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
Qualifications
  • PhD in Pharmaceutical Sciences, Physical/Polymer Chemistry, Material Science, Chemical Engineering, Biomedical Engineering, or related technical field.
  • 5 to 7 years of Medial Device, polymer materials or Pharmaceutical industry experience under a research and development environment.
  • Strong hands-on capability and deep understanding of pharmaceutics and physical chemistry is a must.
Preferred Qualifications
  • Understanding and experience in translation pre-clinical model development
  • Knowledge of major…
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