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Internship Biotech Data Analyst Jobs in Raleigh, NC

... systems, and analytical instrumentation within a regulated pharmaceutical or biotechnology ... Thorough understanding of cGMP regulations, FDA requirements, GAMP 5, 21 CFR Part 11, and data ...

New

Familiarity with requirements gathering, documentation, or systems analysis concepts (academic or internship experience) * Foundational awareness of data concepts (e.g., data flows, data validation ...

Peer review raw data * Order reagents * Participate in assay development and validation * Run ... Analyst III * Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or ...

Peer review raw data * Order reagents * Participate in assay development and validation * Run ... Analyst III * Bachelor's degree in molecular biology, biochemistry, immunology, biotechnology, or ...

Responsible for accurate record keeping with regard to sponsor's samples, data, and reports ... Analyst I * Associate degree in molecular biology, biochemistry, immunology, biotechnology, or ...

Responsible for accurate record keeping with regard to sponsor's samples, data, and reports ... Analyst I * Associate degree in molecular biology, biochemistry, immunology, biotechnology, or ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Strong analytical and collaboration skills, with a desire to work in a regulated, quality-driven ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Strong analytical and collaboration skills, with a desire to work in a regulated, quality-driven ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Strong analytical and collaboration skills, with a desire to work in a regulated, quality-driven ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Strong analytical and collaboration skills, with a desire to work in a regulated, quality-driven ...

Showing results 21-40

Internship Biotech Data Analyst information

See Raleigh, NC salary details

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How much do internship biotech data analyst jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for internship biotech data analyst in Raleigh, NC is $21.88, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $23.85 per hour, depending on experience, location, and employer.

What is the difference between Internship Biotech Data Analyst vs Biotech Data Scientist?

AspectInternship Biotech Data AnalystBiotech Data Scientist
Required CredentialsEnrolled in or recent graduate of related degree (e.g., biology, bioinformatics, data analysis)Advanced degree (Master's or PhD) in data science, bioinformatics, or related fields
Work EnvironmentInternship setting in biotech or pharmaceutical companies, labs, or research institutionsFull-time role in biotech firms, research centers, or biotech startups
Employer & Industry UsageUsed for entry-level training, skill development, and gaining industry experienceUsed for advanced data analysis, modeling, and research projects

The Internship Biotech Data Analyst is an entry-level position focused on gaining practical experience in biotech data analysis, often requiring relevant coursework or a recent degree. In contrast, a Biotech Data Scientist typically holds advanced degrees and performs complex data modeling and research tasks. The internship provides foundational skills, while the data scientist role involves more specialized expertise and responsibilities.

What types of projects or data sets might I work with as an internship biotech data analyst?

As an Internship Biotech Data Analyst, you can expect to work with real-world biological or clinical data, such as genomic sequences, protein structures, or patient trial results. Projects often involve cleaning, analyzing, and visualizing these datasets to support research or product development. You'll likely collaborate closely with scientists, senior analysts, and sometimes software engineers to interpret findings and present actionable insights. This hands-on experience not only strengthens your technical skills but also helps you understand how data analysis drives innovation in the biotech industry.

What are the key skills and qualifications needed to thrive as an internship biotech data analyst, and why are they important?

To thrive as an Internship Biotech Data Analyst, you need a foundation in biology or biotechnology, statistical analysis, and data interpretation, typically gained through coursework or relevant internships. Familiarity with data analysis tools such as Python, R, Excel, and experience with bioinformatics databases or platforms like BLAST is highly beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills make candidates stand out in this role. These competencies are crucial for accurately analyzing complex biological data, supporting research projects, and conveying findings to multidisciplinary teams.

What does an internship biotech data analyst do?

An Internship Biotech Data Analyst supports research and development teams in biotechnology companies by collecting, processing, and analyzing complex biological data. They use statistical tools and software to interpret experimental results, identify trends, and help drive decision-making in projects such as drug discovery, genomics, or clinical trials. Interns often work alongside experienced data analysts and scientists, gaining hands-on experience with real-world datasets and contributing to ongoing research efforts.
What are the most commonly searched types of Biotech Data Analyst jobs in Raleigh, NC? The most popular types of Biotech Data Analyst jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Internship Biotech Data Analyst jobs? Cities near Raleigh, NC with the most Internship Biotech Data Analyst job openings:
Infographic showing various Internship Biotech Data Analyst job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $45,502 per year, or $21.9 per hour.

Senior Validation Engineer

PSC Biotech

Durham, NC

$120K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Job description

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.

Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success.

The Experience

With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At PSC Biotech®, it’s about more than just a job—it’s about your career and your future.

Your Role

We are seeking an experienced Senior Validation Engineer to support commissioning, qualification, and validation activities for laboratory equipment, computerized systems, and analytical instrumentation within a regulated pharmaceutical or biotechnology environment. This individual will lead validation lifecycle activities, including protocol development, execution, deviation management, and final reporting, while ensuring compliance with cGMP, data integrity, and regulatory requirements.
  • Lead and execute commissioning, qualification, and validation activities for laboratory equipment, analytical instruments, utilities, and computerized systems.
  • Develop, review, and execute validation deliverables including Validation Plans, Risk Assessments, IQ/OQ/PQ protocols, Traceability Matrices, and Validation Summary Reports.
  • Author, execute, and review validation documentation within the KNEAT platform.
  • Support Computer System Validation (CSV) activities.
  • Perform risk assessments and apply risk-based validation methodologies throughout the system lifecycle.
  • Collaborate with cross-functional stakeholders to ensure validation activities are executed on schedule and in compliance with site procedures.
  • Support deviation investigations, CAPAs, change controls, and impact assessments associated with validation activities.
  • Provide technical leadership and mentorship to junior validation engineers and project team members.
  • Support internal audits, client audits, and regulatory inspections as needed.
  • Ensure all validation documentation is complete, accurate, and inspection-ready.

Requirements
  • Bachelor's degree in Engineering, Life Sciences, Computer Science, or related technical discipline.
  • Minimum 7+ years of validation, commissioning, qualification, or quality engineering experience within pharmaceutical, biotechnology, medical device, or other FDA-regulated industries.
  • Demonstrated experience with laboratory equipment qualification and analytical instrument validation.
  • Strong Computer System Validation (CSV) experience supporting regulated computerized systems.
  • Hands-on experience using KNEAT for protocol development, execution, review, approval, and lifecycle management.
  • Extensive knowledge of validation lifecycle activities, including:
    • Risk Assessments
    • Validation Plans
    • IQ/OQ/PQ Execution
    • Traceability Management
    • Validation Reporting
    • Change Control
    • Deviation Management
  • Thorough understanding of cGMP regulations, FDA requirements, GAMP 5, 21 CFR Part 11, and data integrity principles.
  • Strong technical writing and documentation skills.
  • Ability to independently manage complex validation projects in a fast-paced environment.
  • Excellent communication, stakeholder management, and cross-functional collaboration skills.
  • Experience supporting regulatory inspections and audit readiness activities preferred.
  • Must be authorized to work in the U.S. No C2C at this time.


Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Long Term Disability and more.
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Discounted rate at Anytime Fitness
  • Financial Perks and Discounts

Equal Opportunity Employment Statement

PSC Biotech is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

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