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Biopharma Internship Jobs (NOW HIRING)

Agilent

Process Engineer

Frederick, CO · On-site

$67K - $105K/yr

Internships or co-ops in the biopharma or chemical industry a plus. Engineering, communication, and organizational skills to support the safe, efficient, and compliant design, construction, and ...

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... equivalent internship or co-op experience in a clinical or pharma setting will be considered.

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... equivalent internship or co-op experience in a clinical or pharma setting will be considered.

Agilent

Process Engineer

Frederick, CO

$67K - $105K/yr

Internships or co-ops in the biopharma or chemical industry a plus. Engineering, communication, and organizational skills to support the safe, efficient, and compliant design, construction, and ...

PCI Pharma Services

Packaging Engineer

Rockford, IL · On-site

Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in ... Participates in recruiting events for interns/co-ops and contributes to the candidate selection and ...

PCI Pharma Services

Packaging Engineer

Rockford, IL

Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in ... Participates in recruiting events for interns/co-ops and contributes to the candidate selection and ...

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Biopharma Internship information

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$2.1K

$6.4K

$7.8K

How much do biopharma internship jobs pay per month?

As of Jul 25, 2026, the average monthly pay for biopharma internship in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What kinds of projects or tasks can I expect to work on during a biopharma internship?

As a biopharma intern, you may be involved in a variety of tasks such as assisting with laboratory experiments, analyzing data from research studies, or supporting quality assurance and regulatory documentation. Interns often collaborate with scientists, engineers, and cross-functional teams to gain hands-on experience in drug development or manufacturing processes. Expect to attend team meetings, contribute to ongoing projects, and possibly present your findings. This exposure helps you develop both technical skills and a deeper understanding of the biopharmaceutical industry.

What is the difference between Biopharma Internship vs Biopharma Associate?

AspectBiopharma InternshipBiopharma Associate
Required CredentialsTypically enrolled in or recent graduate of life sciences or related programsBachelor's or master's degree in life sciences, some roles may require relevant experience
Work EnvironmentTemporary, training-focused, often in research labs or manufacturing facilitiesFull-time, professional setting with responsibilities in research, development, or manufacturing
Employer & Industry UsageInternships offered by biotech and pharma companies for training purposesEntry-level or early-career roles within biotech and pharmaceutical companies

In summary, a Biopharma Internship is a temporary, training-focused position for students or recent graduates, while a Biopharma Associate is a full-time role requiring relevant education and some experience, with greater responsibilities in research or development within the biotech industry.

What are the key skills and qualifications needed to thrive as a Biopharma Intern, and why are they important?

To thrive as a Biopharma Intern, you typically need a background in life sciences or related fields, with foundational knowledge in biology, chemistry, or biotechnology. Familiarity with laboratory techniques, data analysis software (such as Excel or GraphPad Prism), and compliance with safety protocols are commonly required. Strong attention to detail, eagerness to learn, and effective teamwork and communication skills help interns excel in collaborative and fast-paced environments. These skills and qualities are crucial for contributing to research projects, ensuring data integrity, and supporting the overall goals of biopharmaceutical teams.

What are biopharma internships?

Biopharma internships are temporary positions offered by biotechnology or pharmaceutical companies to students or recent graduates interested in gaining hands-on experience in the industry. These internships typically involve working on real-world projects related to drug discovery, research, development, or manufacturing. Interns may assist with laboratory experiments, data analysis, regulatory affairs, or other business functions. The goal is to help interns develop practical skills, industry knowledge, and professional connections that can support their future careers in biopharmaceuticals.
More about Biopharma Internship jobs
What cities are hiring for Biopharma Internship jobs? Cities with the most Biopharma Internship job openings:
What are the most commonly searched types of Biopharma jobs? The most popular types of Biopharma jobs are:
What states have the most Biopharma Internship jobs? States with the most job openings for Biopharma Internship jobs include:
What job categories do people searching Biopharma Internship jobs look for? The top searched job categories for Biopharma Internship jobs are:
Biopharma Internship jobs near you
Infographic showing various Biopharma Internship job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, 1% Contract, 1% Nights, and 1% Summer. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $77,274 per year, or $37.2 per hour.

Senior Process Equipment and Reliability Engineer l

WuXi Biologics

Cranbury, NJ • On-site

$70K - $110K/yr

Full-time

Posted 27 days ago

Job description

Job Title - Senior Process Equipment and Reliability Engineer l
Job Location - Cranbury NJ
Job Summary
The Process Equipment and Reliability Engineer I will provide technical support to ensure safe, reliable, and compliant operation of process and utility equipment within a biopharmaceutical manufacturing facility. An Engineer I will assist with troubleshooting, preventive maintenance, and reliability initiatives while working within cGMP requirements, engineering systems, and reliability methodologies. This role is designed to build foundational skills in equipment engineering and reliability while contributing to daily operations and long-term asset improvement efforts.
Job Responsibilities
Equipment Reliability & Support
  • Assist in monitoring equipment performance and identifying potential reliability risks.
  • Support troubleshooting activities for processing and utility equipment under guidance from senior engineers.
  • Participate in root cause investigations and contribute to corrective and preventive actions (CAPA).
  • Collect and analyze basic equipment data (e.g., downtime, work orders, maintenance history) to support reliability assessments.Maintenance & Asset Management
  • Support the execution of preventive and predictive maintenance programs.
  • Assist in updating and maintaining accurate equipment records in the CMMS system.
  • Help develop and revise maintenance procedures, work instructions, and SOPs.
  • Learn and apply reliability tools such as Failure Modes and Effects Analysis (FMEA) and Reliability-Centered Maintenance (RCM).

Process Equipment Familiarization
  • Gain exposure to upstream, downstream, and fill/finish equipment (e.g., bioreactors, chromatography skids, filtration systems, CIP/SIP systems, autoclaves).
  • Work with operations, maintenance, and senior engineers to understand process-equipment interactions.
  • Support commissioning, qualification, and validation activities for new or modified equipment as assigned.

Compliance & Documentation
  • Ensure all work is completed in accordance with cGMP, FDA, EMA, and internal quality requirements.
  • Draft, revise, and review technical documentation (SOPs, equipment logs, reports) under supervision.
  • Support preparation for audits and inspections by providing accurate documentation and technical input.

Continuous Learning & Improvement
  • Participate in training programs to develop knowledge of biopharma manufacturing equipment, reliability principles, and regulatory compliance.
  • Contribute to continuous improvement projects focused on reducing downtime, improving equipment performance, and increasing operational efficiency.
  • Collaborate with cross-functional teams to learn best practices and support improvement initiatives.

Job Qualifications
  • Bachelor's degree in mechanical, Chemical, Bioprocess, or related Engineering discipline.
  • +2 years of engineering experience; internship or co-op in pharmaceutical, biotech, or regulated manufacturing environment preferred.
  • Basic understanding of process equipment and maintenance concepts.
  • Strong problem-solving and analytical skills with eagerness to learn reliability engineering practices.
  • Ability to work effectively in a team environment and communicate technical information clearly.
  • Familiarity with cGMP or other regulated manufacturing environments is a plus.
  • Proficiency with Microsoft Office tools; exposure to CMMS or data analysis software is desirable.
  • Experience with CMMS systems, asset management practices, and data-driven decision-making.
  • Must work in a self-motivated, highly flexible, well-organized, and detail-oriented style with the requirement of some evening conference call time and occasional local or international travel.
  • Must be able to wear appropriate PPE, ability to stand /sit/walk for long periods of time, ability to lift 50 lbs. occasionally.

Why This Role Matters
This position plays a pivotal role in safeguarding the performance of the facility's most critical assets. Your support will directly influence manufacturing reliability, product quality, and the site's long-term operational strategy. You will have the opportunity to shape how we work, modernize how we manage equipment, and build a culture that values innovation, accountability, and technical excellence.
The anticipated salary for this position is $70,000-110,000
The job description does not intend to list all the duties and responsibilities assigned to this position. An employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and the company's business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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