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Compendial Scientist Jobs (NOW HIRING)

Eurofins Scientific

Routine HPLC Scientist

Cambridge, MA · On-site

$26 - $38/hr

Eurofins Scientific is an international life sciences company, providing a unique range of ... Execute routine analytical assays using electrophoresis, chromatography, and compendial methods to ...

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Compendial Scientist information

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How much do compendial scientist jobs pay per year?

As of Jul 10, 2026, the average yearly pay for compendial scientist in the United States is $68,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $59,500.00 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.
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Compendial Scientist jobs near you

Senior Associate Scientist, Quality Control

WuXi Biologics

Cranbury, NJ • On-site

$54K - $87K/yr

Full-time

Re-posted 29 days ago

Job description

Job Title - Senior Associate Scientist, Quality Control - RM/Compendial Testiing and Sampling
Work Location - Cranbury NJ
Job Summary
The QC RM/Compendial Scientist is responsible for the quality and on-time completion of raw material/compendial testing and sampling. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates good oral and written communication skills and actively contributes to timely training, report generation and good GMP documentation and archival.
Job Responsibilities
  • Understand GMP and follow instructions on the documents.
  • Perform raw material/compendial testing including but not limit to FTIR, pH, Color, Clarity, visible and subvisible particles, osmolarity, etc.
  • Able to support Raw Material sample sampling and its transporting needs in/between the various building sites in Cranbury or other US sites (when needed).
  • Management of raw material samples, raw material sampling room, sample storage room and regulatory retain sample room, etc., and ensuring the sampling process and storage of raw material samples are conducted properly and within control.
  • Support reagents/consumables inventory management to ensure consistent QC RM/Compendial operation needs.
  • Record and organize experimental data in accordance with "Good Document Management Practices" to ensure data integrity.
  • Ensure compliance to training, preparation, documentation and general lab maintenance requirements for Industry Standards and/or Regulations.
  • Assist in preparing or executing validation documents to support new materials, process changes and qualifications.
  • Maintains laboratory notebooks and worksheets for QC tasks as required.
  • Able to work at weekend when needed.
  • Support shift work when needed.
  • Any other duties assigned by the supervisor (when applicable).

Qualifications
  • Full-time undergraduate degree or above, majoring in biology, chemical engineering, chemistry, pharmacy or related majors.
  • Bachelor's degree: 6+ years of experience in the professional field
  • Master's degree: 4+ years of experience in the professional field
  • PhD: no requirement
  • Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
  • Basic familiarity with analytical instruments and methodologies, such as pH, turbidity meter, HIAC, etc, is preferred.
  • Basic experience with software and information systems (eg. TrackWise, Master Control, LIMS). Ability to adapt between strategic and tactical thinking/planning and manage multiple priorities to achieve department and site objectives.
  • Ability to understand technical data
  • Experience in planning and ability to solve QC technical and operation problems.
  • Be able to raise issues immediately to supervisor and work with supervisor when in doubt.
  • Proficiency in English is required. Good communications skills (verbal, written, and presentation skills).
  • Effectively exchange information or discuss clearly framed issues or ideas with colleagues.

The anticipated pay range for this position is $54,000 - $87,000
The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.

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