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Drug Product Process Development Intern Jobs (NOW HIRING)

Development Intern

Portland, OR · On-site

$16 - $21.25/hr

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Drug Product Process Development Intern information

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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.

Manufacturing Specialist 1, Drug Product Process

Holly Springs, NC • On-site

Fujifilm
Chemical Manufacturing • 10K+ employees

Full-time

Medical, Retirement, PTO

Re-posted 18 days ago


Fujifilm rating

8.6

Company rating: 8.6 out of 10

Based on 71 frontline employees who took The Breakroom Quiz


Job description

Help bring life-changing medicines to patients by ensuring reliable, compliant manufacturing. As a Manufacturing Specialist I, DP, you’ll be a hands-on problem solver and process SME who keeps operations running smoothly in a 24/7 environment—driving documentation excellence, tech transfer readiness, and continuous improvement across Drug Product Finished Goods.


FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together!


Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.


Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers


About Us We are a high-growth, 24/7 biopharmaceutical manufacturing site focused on delivering high-quality drug products safely and efficiently. Our team values collaboration, learning, and operational excellence. You’ll join a global, cross-functional community where your voice matters and your work makes a direct impact on patients.

Responsibilities

  • Support operational readiness during the project phase, including site commissioning and qualification efforts.
  • Troubleshoot process issues and act as a process subject matter expert (SME) for assigned area(s).
  • Coordinate batch planning, including process template creation, import, and the management of Preventative Maintenance (PMs).
  • Own, perform, or drive major documentation updates (including initiating new documents for new processes).
  • Coordinate non-batch activities such as changeover, PMs, and Aseptic Process Simulation (APS).
  • Support MSAT with technology transfer activities within manufacturing.
  • Ensure manufacturing operations adhere to all compliance and safety procedures.
  • Create and update Electronic Batch Records (EBRs) and Paper Batch Records.
  • Manage, perform, initiate, or support change management records, investigations, Corrective and Preventive Actions (CAPAs), and Continuous Improvement (CI) activities.
  • Manage projects, lead execution, and participate in projects within Drug Product Finished Goods.
  • Assist and support inspections and audits to ensure compliance in the manufacturing environment.
  • Assist the Manager with projects and training, as needed.
  • Collaborate effectively in small, cross-functional teams; mentor and guide junior associates.
  • Flexibility with working hours and shift rotation to support a 24/7 manufacturing facility.

Within this role, you’ll be successful if you bring:

  • Strong verbal and written communication skills.
  • Strong time management skills.
  • Ability to adapt in a fast-paced environment, pivot, and adjust plans accordingly.
  • Ability to think critically and demonstrate superior problem-solving skills.
  • Ability to analyze and troubleshoot simple to moderate system and component-related issues.
  • Ability to coordinate and facilitate effective small cross-functional teams.
  • Ability to mentor and guide junior-level associates.
  • Ability to effectively present information to others.
  • Team-based attitude and ability to work in a global team environment, build relationships, and communicate effectively with others.

Minimum Qualifications

  • High School Diploma or Equivalent with 9 years of applicable industry experience OR
  • Bachelor’s degree with 5 years of applicable industry experience OR
  • Master’s degree with 3 years of applicable industry experience OR
  • PhD without experience OR
  • Equivalent Military Experience

Preferred

  • High degree of understanding of operations sequence and cadence of activities in a manufacturing environment.

Benefits

  • Competitive compensation with potential shift differentials for 24/7 operations.
  • Comprehensive health and wellness benefits.
  • Retirement savings and financial wellness support.
  • Paid time off, paid holidays, and flexible scheduling where business needs allow.
  • Professional development, mentorship, and training opportunities.
  • Inclusive, team-oriented culture with global collaboration and opportunities to grow your career.
  • Recognition programs and opportunities to lead and influence process improvements.

We welcome applicants from all backgrounds and experiences. If you’re excited to contribute to safe, compliant, and efficient manufacturing—and to grow your impact in a collaborative environment—we’d love to hear from you. Apply today.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.


Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.


If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).


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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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