Career CategoryOperations
Job DescriptionProcess Development Associate Scientist What you will doLet's do this. Let's change the world. In this vital role you will join Pre-Pivotal Drug Product Technologies group, responsible for early-stage drug product development across diverse modalities, with a strong emphasis on monoclonal antibodies, multispecifics and other biologic modalities. The role involves designing and developing liquid and lyophilized formulations; evaluating critical quality attributes (CQAs); establishing robust, scalable fill/finish processes for complex biologic drug products; and authoring and supporting high quality regulatory submissions.
- Plan and execute formulation, stability, end-use compatibility, and fill/finish process studies for early-stage programs.
- Develop and characterize liquid and lyophilized formulations for biologics, with particular emphasis on biologics drug product formulation, handling, and lab-scale sterile filling.
- Investigate biologics-relevant CQAs (e.g., aggregation, fragmentation, charge/size variants, subvisible particles, surface interactions) to inform formulation and process design decisions.
- Design, develop, and execute automated high-throughput formulation screening workflows to accelerate excipient selection, formulation optimization, and processability assessments.
- Develop and implement laboratory automation solutions, including robotic liquid handling systems and automated sample preparation workflows, to improve experimental throughput, reproducibility, and data quality.
- Utilize design of experiments (DoE), high-throughput experimentation, and automated data analysis pipelines to efficiently explore formulation design space and support data-driven decision making.
- Identify and address technology gaps impacting biologics stability, protein-excipient interactions, and process-related stress responses.
- Apply machine learning, AI, laboratory automation, and data science to predictive modeling, workflow acceleration, and decision-making.
- Author/review guideline documents, technical protocols, technical transfer documentation, reports, product impact assessments, and regulatory sections in support of IND submissions
- Meticulous data collection, documentation using electronic data capture systems
- Ability to work in a matrixed team and present data cross functionally
What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:Master's degree
OR
Bachelor's degree and 2 years of
Scientific experience
OR
Associate's degree and 4 years of
Scientific experience
OR
High school diploma / GED and 6 years of
Scientific experience
Preferred Qualifications:- Master's degree in Pharmaceutics, Biotechnology, Biochemistry, Physical Biochemistry, Biophysics, Chemical Engineering, or related field with a minimum of 3+ years of industrial experience in pharmaceutical/biotechnology or related field
- Understanding of physical/chemical stability of proteins and how process related stress impacts product quality.
- Preferred experience in biophysical analysis (Light scattering, DSF, AUC, FFF) and mass spectrometry (peptide mapping).
- Ability to learn and act on dynamic information at a rapid pace, hard-working and collaborative attitude
- Excellent oral and written communication skills for timely documentation, presentation, and discussion of scientific results for a fast pace and cross functional environment.
- Proven experience in formulation development and fill/finish operations for biologics; direct biologics drug product formulation experience is strongly preferred.
- Hands-on experience with high-throughput formulation development, automated liquid handling systems (e.g., Hamilton, Tecan, Beckman Coulter, Opentrons, or equivalent), and robotic laboratory workflows.
- Experience implementing laboratory automation, workflow digitization, and electronic data capture to improve R&D productivity.
- Familiarity with DoE, high-throughput experimentation, laboratory robotics, and workflow orchestration for formulation and process development.
- Strong foundation in analytical techniques relevant to biologics and biologics (e.g., UPLC/HPLC, SEC, IEX, RP-HPLC, HIC, CE-SDS, subvisible particle analysis, etc.).
What you can expect from usAs 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.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.comSalary Range90,442.55USD -122,363.45 USD
