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Compendial Scientist Jobs in Missouri (NOW HIRING)

Manager, Biochemical Analysis

Kansas City, MO · On-site

$18 - $20/hr

In this role, you will lead sub-teams of group leaders, scientists, and associate scientists ... Provide expertise in techniques such as compendial assays, Karl Fischer, UV-Vis, HPLC/UPLC methods ...

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Compendial Scientist information

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.

What cities in Missouri are hiring for Compendial Scientist jobs?

Cities in Missouri with the most Compendial Scientist job openings:

Infographic showing various Compendial Scientist job openings in Missouri as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 7% Part Time, and 5% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Manager, Biochemical Analysis

Catalent Pharma Solutions

Kansas City, MO • On-site

Full-time

Medical, Dental, Vision, Life, PTO

Posted 13 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

60th of 86 rated pharmaceutical


Job description

Manager, Biochemical Analysis Role

About Site

Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Manager, Biochemical Analysis to join our team. In this role, you will lead sub-teams of group leaders, scientists, and associate scientists, serving as a technical expert and key liaison between clients and internal teams. You will oversee analytical activities for biopharma product development under cGMP guidance, ensuring quality, compliance, and timely delivery. This position also involves mentoring, HR responsibilities, and supporting audits and client interactions.

Shift: Monday - Friday, Day Shift
Location: Kansas City, MO
100% Onsite

The Role

  • Manage technical analysis, production scheduling, and resolve operational issues, escalating critical concerns when needed.

  • Oversee people management, including coaching, performance management, and career development. Lead and develop high-performing teams, including group leaders, scientists, and associate scientists.

  • Serve as technical expert on projects and act as liaison between clients and Catalent technical teams.

  • Handle HR activities such as performance reviews, time entry approval, PTO approval, and salary adjustments.

  • Support client audits and visits, and communicate with cross-functional teams on analytical activities for biopharma product development under cGMP guidance.

  • Provide expertise in techniques such as compendial assays, Karl Fischer, UV-Vis, HPLC/UPLC methods, aggregation techniques, electrophoresis, FTIR, CD, fluorescence, DSC, and other technologies as required.

  • Supervise method development, evaluation, transfers, verifications, qualifications, validations, stability studies, and ad hoc sample testing.

  • Plan, prioritize, and execute analytical work in compliance with client contracts and technical agreements. Serve as backup or lead Project Technical Lead as needed.

  • Manage computer system validation activities and ensure equipment compliance. Ensure adherence to cGMP practices and maintain data integrity and quality.

  • Verify analytical data and ensure compliance with SOPs and safety legislation. Assist in project costing, timelines, and monitor budgets and revenue forecasts. Communicate effectively with clients, auditors, peers, and leadership to ensure smooth project execution.

  • Coordinate training needs and maintain team engagement and growth culture. Support marketing and business development activities and stay updated on modern techniques.

  • Identify and implement new technologies and model Catalent's culture of quality, safety, and ethics.

  • All other duties as assigned

The Candidate

  • Bachelor's degree with more than 5 years of relevant experience in department-specific techniques and over 2 years of management experience preferred, or based on performance at Catalent.

  • Master's degree with more than 3 years of relevant experience in department-specific techniques and over 1 year of management experience preferred, or based on performance at Catalent.

  • Doctorate degree with more than 2 years of relevant experience in department-specific techniques and over 1 year of management experience preferred, or based on performance at Catalent.

  • Demonstrable leadership experience at Catalent (including but not limited to participation in Catalentsponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

  • Strong knowledge of principles, theories, and concepts in Biology, Chemistry, or Biochemistry, and broad understanding of related disciplines.

  • In-depth expertise in instrumentation, theory, data interpretation, and applications in at least one technical area, with ability to assess new technologies and their impact on Catalent offerings.

  • Experience in drug development and lifecycle support, with ability to develop strategies to meet regulatory milestones.

  • Excellent written and verbal communication skills for internal and external stakeholders.

  • Ability to explain complex technical information to non-technical audiences.

Why You Should Join Catalent

  • Defined career path with annual performance reviews and feedback process.

  • Diverse and inclusive culture.

  • Opportunities for career growth within an organization dedicated to improving lives.

  • Competitive paid time off plus 8 paid holidays.

  • Community engagement and green initiatives.

  • Medical, dental, and vision benefits effective from day one.

  • Tuition reimbursement program.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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