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Compendial Scientist Jobs (NOW HIRING)

Civica Rx

Senior Scientist - Biologics

Petersburg, VA · On-site

$89K - $122K/yr

... compendial method verification (endotoxin, bioburden, sterility), and ensures methods are suitable for the product • Critically review and approve bioassay protocols; provide scientific direction ...

Civica Rx

Senior Scientist - Biologics

Petersburg, VA · On-site +1

$110K - $145K/yr

... compendial method verification (endotoxin, bioburden, sterility), and ensures methods are suitable for the product • Critically review and approve bioassay protocols; provide scientific direction ...

kindeva

Scientist III

Bridgeton, MO

The Analytical Development Scientist III functions as a senior technical expert within the QC ... Work must comply with cGMP regulations, compendial standards (USP/NF, EP), site policies, and ...

Piramal Pharma Limited

Scientist II

Lexington, MA

Be the First to Apply Scientist IIBusiness: Pharma Solutions Department: Analytical R&D (ARD ... and compendial test methods. Executes proficiency in development and transfer/verification ...

kindeva

Scientist III

Bridgeton, MO

The Analytical Development Scientist III functions as a senior technical expert within the QC ... Work must comply with cGMP regulations, compendial standards (USP/NF, EP), site policies, and ...

MyGradJob

Senior Scientist

North Chicago, IL

$88K - $120K/yr

APPLY HERE!!!! mygradjob.com/job/senior-scientist-8/ We are looking for a highly motivated person ... ELISA, compendial tests * Broad expertise around regulatory requirements for NBEs (mAbs ...

kindeva

Scientist III

Bridgeton, MO

The Analytical Development Scientist III functions as a senior technical expert within the QC ... Work must comply with cGMP regulations, compendial standards (USP/NF, EP), site policies, and ...

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Compendial Scientist information

See salary details

$57.5K

$68K

$129K

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
Associate QC Scientist

Associate QC Scientist

Artech Information System LLC

Devens, MA

Contractor

Posted 8 days ago

Job description

Company Description

Big Pharmaceutical Organisation

Job Description
  1. Support raw material qualifications, method transfers, and validation of assays such as UV-VIS Spectrometry, SDS Page, wet chemical analysis, utility testing (e.g. TOC, conductivity, and gas testing) and more complex assays including GC solvent analysis and various HPLC methodologies (e.g. peptide map and carbohydrate analysis). 
  2. Review compendial methods (USP, EP, JP) for alignment with internal raw material test procedures and specifications.
  3. Perform routine/non-routine data analysis calculations.
  4. Document analytical data under cGMP and corporate guidelines.
  5. Participate and resolve laboratory investigations of unexpected analytical results.
  6. Write/review SOPs, test methods, material specifications, validation protocols and reports.
  7. Support cGMP laboratory initiatives following laboratory SOPs.
  8. Other duties may be assigned.
Qualifications

Bachelor's degree in chemistry, biochemistry, or related scientific discipline required.
Master's degree preferred.

6 years experience with a Bachelors or 4 years with a Masters 

Additional Information

Interested candidates may contact at Praveen.arora at artechinfo.com or 973-507-7593

Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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