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Compendial Scientist Jobs in Raleigh, NC (NOW HIRING)

Bachelor's degree in scientific discipline with 0-1 years of experience Preferred Requirements ... Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing ...

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Bachelor's degree in scientific discipline with 0-1 years of experience Preferred Requirements ... Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing ...

New

Bachelor's degree in scientific discipline with 0-1 years of experience Preferred Requirements ... Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing ...

New

Bachelor's degree in scientific discipline with 0-1 years of experience Preferred Requirements ... Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing ...

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Compendial Scientist information

See Raleigh, NC salary details

$55.9K

$66.1K

$125.4K

How much do compendial scientist jobs pay per year?

As of Jul 14, 2026, the average yearly pay for compendial scientist in Raleigh, NC is $66,139.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,400.00 and $57,800.00 per year, depending on experience, location, and employer.

What is the difference between Compendial Scientist vs Quality Control Analyst?

AspectCompendial ScientistQuality Control Analyst
Required credentialsBachelor's degree in life sciences, certifications in GMP/GLPBachelor's degree in sciences, certifications in GMP/GLP
Work environmentLaboratories, regulatory agencies, pharmaceutical companiesLaboratories, pharmaceutical manufacturing facilities
Employer and industry usageUsed in regulatory compliance, ensuring products meet pharmacopeial standardsUsed in testing and analyzing raw materials and finished products

Compendial Scientists focus on ensuring products meet pharmacopeial standards and regulations, often working on documentation and compliance. Quality Control Analysts primarily perform testing and analysis of samples to verify product quality. Both roles require similar credentials and work environments, but their core responsibilities differ in scope and focus.

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

To thrive as a Compendial Scientist, you need a strong background in analytical chemistry, regulatory compliance, and scientific documentation, typically supported by a degree in chemistry, pharmacy, or a related field. Familiarity with laboratory instrumentation (such as HPLC, GC, and spectroscopy), compendial standards (USP, EP, JP), and quality management systems is essential. Attention to detail, critical thinking, and effective communication help ensure accuracy and clear documentation of results. These skills and qualities are crucial to maintain product quality, meet regulatory requirements, and support successful audits in the pharmaceutical industry.

What are some common challenges faced by Compendial Scientists when ensuring compliance with evolving pharmacopeial standards?

Compendial Scientists often encounter the challenge of staying current with frequently updated pharmacopeial standards and ensuring that laboratory methods and documentation remain fully compliant. This requires constant monitoring of regulatory changes, rapid adaptation of procedures, and effective collaboration with quality assurance, regulatory affairs, and analytical development teams. Timely communication and robust project management skills are essential to implement changes without disrupting ongoing operations. Proactively engaging in cross-functional meetings and training sessions can help address these challenges and ensure seamless compliance.

What are Compendial Scientists?

Compendial Scientists are professionals who specialize in ensuring that pharmaceutical products comply with standards set by official compendia, such as the United States Pharmacopeia (USP) or the European Pharmacopoeia (Ph. Eur.). They review, interpret, and implement compendial requirements into a company's quality control processes and documentation. Their work often involves collaborating with regulatory agencies, staying current with changes in compendial standards, and participating in the development or revision of monographs and methods. Compendial Scientists play a critical role in maintaining product quality, safety, and regulatory compliance in the pharmaceutical industry.
What cities near Raleigh, NC are hiring for Compendial Scientist jobs? Cities near Raleigh, NC with the most Compendial Scientist job openings:
Analyst 1, QC Microbiology

Analyst 1, QC Microbiology

Fujifilm

Holly Springs, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

51st of 527 rated manufacturers


Job description

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


The Analyst, QC Microbiology is responsible for the key operational aspects of the QC Microbiology laboratory. This role performs microbial testing of all in-process drug substance, drug product, EM/UM, and raw materials samples under minimal supervision. The Analyst, QC Microbiology is responsible for all activities associated with testing in accordance with written procedures. This role participates in writing or assisting with document preparation and review, managing project timelines, conducting qualification and validation protocols, and assisting management with training and on-boarding of new staff, as needed and in addition to regular work duties and assignments.


What You'll Do:

  • Supports environmental and utilities monitoring sample collection
  • Provides input to define protocols for sample collection and logistics, ensuring compliance with regulatory standards
  • Coordinates testing materials and supplies
  • Plans and ensures materials are stocked. Partners with procurement, inventory management, and distribution to optimize laboratory operations
  • Performs advanced microbiology testing by generating complex test data for in-process samples, raw materials, and environmental samples, providing analysis for Bioburden, Endotoxin, and microbial findings
  • Performs Sterility testing and validation processes and participates in isolator qualification procedures and ensures effective routine operations and maintenance
  • Ensures accuracy and security of laboratory information, implementing tools and protocols for data management
  • Conducts comprehensive reviews of laboratory testing results and provides analysis and interpretation of results, identifying trends and making informed recommendations
  • Under the direction of management, troubleshoots issues with laboratory assays and identifies underlying causes of assay failures and develops strategic solutions to improve test reliability
  • Leads general laboratory support and maintenance initiatives by maintaining analytical instruments and laboratory resources, coordinating
    purchases and receipt of essential supplies
  • Supports implementation and monitoring of CAPAs
  • Partners with management to initiate and coordinate resolution for deviations and non-conformance events within quality systems
  • Participates in project developments from concept through execution, ensuring alignment with organizational goals
  • Performs additional duties, as needed

Minimum Requirements:

  • Bachelor’s degree in scientific discipline with 0-1 years of experience

Preferred Requirements:

  • BS within Microbiology, Chemistry, Biochemistry, Biology
  • 2+ years of Intermediate experience in a GMP QC Microbiology
  • Laboratory, knowledge of all compendial test methods (Bioburden, Endotoxin, sterility testing) preferred
  • Ability to troubleshoot and maintain laboratory equipment and instrumentation
  • Experience with microbial ID systems (MALDI, MicroSeq)

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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