×
Register Here to Apply for Jobs or Post Jobs. X

Process Development Principal Scientist

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Amgen SA
Full Time position
Listed on 2026-03-12
Job specializations:
  • Engineering
    Research Scientist, Biotechnology
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Process Development Principal Scientist

What you will do

Let’s do this. Let’s change the world. In this vital role you will join our Pivotal Drug Product Technologies group in Cambridge, MA. This group supports drug product commercial formulation development as well as formulation/fill/finish process development for Amgen’s Late-Stage biologics. The Principal Scientist will provide technical and project leadership while integrating information generated by functionally diverse teams to ensure success through the commercialization process.

  • Delivering progress reports and presentations to ensure management awareness and engagement of the status, progress, and future program and functional needs
  • Authoring and reviewing guideline documents, technical protocols, reports, product impact assessments, regulatory submissions, and developing responses to regulatory questions
  • Driving continuous improvement in the drug product development process through technological innovation and application of first principles in process engineering
  • Serving as subject matter expert and help drive standard methodologies and technical advancements
  • Serving as a Drug Product Team Lead of matrixed team to develop strategy in support of commercialization and life cycle management of Amgen’s pipeline
  • Managing a team of engineers and scientists to advance program and functional objectives
  • Expanding utilization of advanced IS systems to improve drug product design through faster data availability, using historical information, analyzing large data sets, and statistical analysis
  • Working effectively in a highly matrixed team environment to influence and inspire change, efficiency, and foster positive relationships
  • Ability to travel domestically and internationally up to 10% of the time.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Scientific professional we seek is an individual with these qualifications.

Basic Qualifications:

  • Doctorate degree PhD OR Pharm

    D OR MD and 2 years of Scientific experience OR
  • Master’s degree and 5 years of Scientific experience
    OR
  • Bachelor’s degree and 7 years Scientific experience

Preferred Qualifications:

  • Advanced degree in Engineering, Pharmaceutics, Biotechnology, Material Science or related subject area
  • 8+ years of experience in pharmaceuticals/biotechnology
  • 5+ years of experience that includes elements of formulation and fill/finish process development, process characterization, technical transfers to manufacturing sites, and statistical design and analysis of experiments, and regulatory authoring
  • Technical leader with demonstrated results driving forward programs
  • Experience in drug product regulatory strategy, RTQs, and agency engagement
  • Knowledge of, and hands‑on experience with, bringing new biotech products to market, across various dosage forms and device delivery systems
  • Experience with programming (e.g. Python, R, MATLAB) and database languages (e.g. SQL), as well as data visualization tools (e.g. Tableau, Spotfire, D3js)
  • Proficiency in at least one statistical software package…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary