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How much do drug product process development intern jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for drug product process development intern in the United States is $21.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What does a drug product process development intern do?

A Drug Product Process Development Intern assists in the development and optimization of manufacturing processes for pharmaceutical products. They typically work alongside scientists and engineers to support formulation development, process characterization, and scale-up activities. Interns may conduct laboratory experiments, analyze data, and help ensure that processes comply with regulatory standards. This role provides hands-on experience in the pharmaceutical industry and helps interns understand the complexities of drug product development.

What types of projects and responsibilities can a drug product process development intern expect to work on during their internship?

As a Drug Product Process Development Intern, you can expect to assist with the design, execution, and analysis of experiments related to formulation and manufacturing processes for pharmaceuticals. You’ll often work closely with scientists and engineers to optimize processes, prepare lab-scale batches, and document results for regulatory compliance. Collaboration with cross-functional teams such as Analytical Development and Quality Assurance is common, giving you exposure to multiple aspects of drug development. Interns may also be involved in troubleshooting process issues and contributing to continuous improvement initiatives.

What are the key skills and qualifications needed to thrive as a drug product process development intern, and why are they important?

To thrive as a Drug Product Process Development Intern, you need a strong background in pharmaceutical sciences, chemistry, or chemical engineering, often supported by current enrollment in a relevant degree program. Familiarity with laboratory techniques, data analysis software, and Good Manufacturing Practices (GMP) is typically expected. Strong attention to detail, problem-solving abilities, and effective teamwork are essential soft skills in this role. These competencies enable interns to contribute meaningfully to drug formulation projects while maintaining compliance and fostering innovation in a highly regulated environment.

What are popular job titles related to Drug Product Process Development Intern jobs?

For Drug Product Process Development Intern jobs, the most frequently searched job titles are:

Infographic showing various Drug Product Process Development Intern job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.

Process Development Principal Scientist - Drug Product Technologies

Thousand Oaks, CA • On-site

Amgen SA
See more jobs at Amgen SAexternal

Other

Posted 23 days ago

Job description

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 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 the Pre-Pivotal Drug Product Technologies group, which is responsible for early‑stage drug product development across diverse modalities, including antibody‑drug conjugates (ADCs), oligonucleotides such as siRNAs, monoclonal antibodies, multispecifics, and other complex biologics. The role involves designing and developing liquid and lyophilized formulations; evaluating critical quality attributes (CQAs); establishing robust, scalable fill/finish processes; and authoring and supporting high‑quality regulatory submissions.

The ideal candidate will bring hands‑on experience and leadership in biologics drug product formulation, process development, and/or analytical characterization, with experience in ADCs and/or oligonucleotides such as siRNAs strongly preferred. The candidate will integrate formulation, analytical, stability, and process data to guide product design and development, including modality‑specific considerations such as linker‑payload attributes, stability‑and process‑relevant degradation pathways, ADC CQAs, oligonucleotide formulation and stability considerations, and phase‑appropriate analytical strategies. This individual will apply scientific judgment, emerging technologies including AI/ML, and strong cross‑functional collaboration to deliver high‑quality, stable, and manufacturable drug products for clinical development in a fast‑paced environment.

  • Serve as a leader on Drug Product teams responsible for planning, designing, executing, and documenting laboratory studies related to drug product design, formulation, process development, technology transfer, and regulatory authoring in support of advancing Amgen’s diverse biologics pipeline.
  • Work effectively in a fast‑paced, matrixed environment, collaborating across process development, research, analytical, regulatory, quality, manufacturing, and external partner teams to advance programs, influence development strategies, and communicate technical recommendations to scientific peers and leadership.
  • Develop and characterize liquid and lyophilized formulations for complex biologics, including ADCs, oligonucleotides, monoclonal antibodies, multispecifics, and other emerging modalities.
  • Build process understanding across unit operations to support scalable drugproductdevelopment.
  • Evaluate in‑use compatibility and drug product stability under clinically relevant conditions.
  • Investigate biologics‑and modality‑relevant CQAs, including aggregation, fragmentation, charge and size variants, subvisible particles, surface interactions, concentration‑dependent behavior, and
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