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Compendial Scientist Jobs in Chicago, IL (NOW HIRING)

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 ...

CYNET SYSTEMS

Scientist I (B Shift)

Melrose Park, IL · On-site

$20 - $21/hr

Bachelor of Science degree in a biological science with 1-3 years progressive laboratory experience ... Maintains knowledge of current compendial methods. * Teaches or coordinates teaching of training ...

CYNET SYSTEMS

Scientist I (B Shift)

Melrose Park, IL · On-site

$20 - $21/hr

Bachelor of Science degree in a biological science with 1-3 years progressive laboratory experience ... Maintains knowledge of cGMPs and GLPs and current compendial methods. * Teaches or coordinates ...

All JobsCompendial Scientist JobsCompendial Scientist Jobs in Chicago, IL

Compendial Scientist information

See Chicago, IL salary details

$59.2K

$70.1K

$132.9K

How much do compendial scientist jobs pay per year?

As of Aug 31, 2026, the average yearly pay for compendial scientist in Chicago, IL is $70,090.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,800.00 and $61,300.00 per year, depending on experience, location, and employer.

What is a compendial scientist?

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 are the key skills and qualifications needed to thrive as a compendial scientist?

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 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.

Compendial Scientist jobs near you
Infographic showing various Compendial Scientist job openings in Chicago, IL as of July 2026, with employment types broken down into 1% Locum Tenens, 9% Internship, 33% As Needed, 50% Full Time, 3% Part Time, and 4% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $70,090 per year, or $33.7 per hour.

Senior Scientist

MyGradJob

North Chicago, IL

$88K - $120K/yr

Full-time

Re-posted 12 days ago

Job description

Company Description

AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most complex and serious diseases. AbbVie employs approximately 28,000 people worldwide and markets medicines in more than 170 countries.

Job Description
APPLY HERE!!!!      mygradjob.com/job/senior-scientist-8/    
We are looking for a highly motivated person who drives new technologies and processes. The candidate will develop drug product formulations and scalable manufacturing processes for NBEs used in clinical trials through all phases of development. Working closely with analytical and formulation scientists in an integrated group the candidate will operate via multi-functional, global teams including API manufacturing, Process R&D, Pre-formulation and Pilot Plant Operations. 
 
Major Responsibilities
  • The incumbent will participate in the development of parenteral formulation for monoclonal antibodies and antibody drug conjugates,
  • Independently design and execute studies evaluating the stability (chemical & physical) of the monoclonal antibodies and antibody constructs/conjugates against solution conditions (pH, ionic strength, temperature, light  e.tc) and physical stresses arising from manufacturing process conditions (freeze thaw, mixing, filtration, filling, filtration and Lyophilization), and screen excipients (buffers, stabilizers, surfactants, tonicity & Tg' modifiers e.t.c) to develop robust formulations for frozen, refrigerated liquid and lyophilized dosage forms
  • Perform upfront manufacturability assessment of the formulation candidates and recommend the best and back up formulation for both FIH and commercialization
  • Make concise scientific presentations of experimental results to the management and author detailed scientific technical reports.
  • Author CMC relevant sections of INDs/CTDs, as well as response questions
  • scientific project lead, generating original technical ideas for formulation and analytical technologies of assigned NBE development projects 
  • Establishment and coordination of external development activities including supervision of technical, financial and regulatory requirements 
Qualifications

Basic:

  • BS and typically 10+ years of experience; MS or equivalent education with typically 8+ years of experience; PhD 0+ years of experience in formulation or analytical development of NBEs 
  • Scientific understanding of the structure & function of monoclonal antibodies and antibody constructs/conjugates, and their modes of degradation/stabilization
  • An understanding of scientific approach to develop biologic protein formulations
  • Strong lab skills focused on formulation development for monoclonal antibodies and antibody constructs/conjugates (standard excipient selection, functional excipients, high throughput assays)
  • Basic understanding of unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized NBEs 
  • Hands on expertise of bio analytical test methods for protein pharmaceuticals e.g. mass-spectrometry, HPLC and electrophoretic methods, particle imaging, ELISA, compendial tests
  • Broad expertise around regulatory requirements for NBEs (mAbs, bispecifics, ADCs) and parenteral products is preferred (21 CFR parts  600 & 210, FDA cGMP-, ICH-, EU GMP-guidances). 
  • Statistical knowledge and experience is preferred e.g. capability analysis, gauge R&R and design of experiments (DOE) methodologies 
Additional Information

All your information will be kept confidential according to EEO guidelines.

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