Process Development Associate Scientist

Process Development Associate Scientist

What you will do

Let’s do this. Let’s change the world. As a Process Development Associate Scientist, you will play an integral part in Amgen’s Late-Stage Synthetics and Commercial Drug Product team within the Drug Product Technologies department. Your responsibilities will center around gaining practical experience and offering hands-on expertise in formulation and process development for Amgen’s synthetics pipeline. The core activities of this group involve developing clinical, robust commercial formulations and life cycle management initiatives for a wide array of Amgen’s synthetic assets.

This position provides the unique opportunity to collaborate with skilled scientists and contribute to the advancement and launch of innovative synthetic drug products across a variety of oral or parenteral dosage forms. Through your work, you will support both the development and commercialization phases, ensuring that Amgen continues to deliver cutting-edge solutions for patients worldwide.

• Hands-on experience in spray-drying formulation and process development, including experimental design, process optimization, data analysis, and characterization of spray-dried materials.

• Understanding of spray-drying process scale-up from laboratory to manufacturing scale, including equipment considerations, technology transfer, process troubleshooting, and identification of critical process parameters and quality attributes.

• Interface within the Drug Product Technologies Department as a team member to support programs and initiatives.

• Contribute to the completion of experimental design and execution and assist in the analysis and interpretation of data.

• Utilize digital tools and emerging AI-enabled solutions to improve experimental efficiency, data analysis, and scientific insight generation.

• Contribute to technical problem-solving efforts and identify opportunities for automation and digital solutions to improve efficiency and reduce repetitive manual tasks.

• Actively contribute to process improvements, strategy development, and cross-functional partnerships that promote consistent and efficient practices across late-stage clinical and commercial synthetic programs.

• Organize and communicate information within the team to help lead to the best possible formulation and processes.

We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a collaborative partner with these qualifications.

Basic Qualifications:

• Master’s degree and 1 years of scientific experience

• OR

• Bachelor’s degree and 3 years of scientific experience

Preferred Qualifications:

• Master’s degree in Pharmaceutical Sciences, Chemical or Pharmaceutical Engineering, Chemistry, or a life sciences-related field, with relevant industry experience.

• Understanding of the typical unit operations for the manufacture of oral solid dosage forms (i.e., granulation, roller compaction, drying, milling, blending, compression, film coating, etc.).

• Basic understanding of the physical and chemical stability of synthetic molecules, enabling formulations, amorphous solid dispersions, and how manufacturing processes, including spray drying, HME, roller compaction, and compression, impact product quality.

• Ability to design, execute, and interpret experimental results.

• Strong problem-solving skills applied to the formulation and characterization of parenteral and oral synthetic molecules.

• Excellent written and verbal communication skills for presenting scientific results in a fast-paced, multi-disciplinary environment.

• Proven ability to work effectively in collaborative, team-based settings.

• A proactive, curious, and innovative mindset, with enthusiasm for applying digital solutions to scientific challenges

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship for this role is not guaranteed.

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Salary Range