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Analytical Development Jobs in Missouri (NOW HIRING)

Kindeva Drug Delivery

Scientist II

Saint Louis, MO · On-site

The Impact You Will Make As an Analytical Development Scientist II, you will play a critical role in supporting analytical method transfer, verification, and validation activities for both small ...

kindeva

Scientist III

Bridgeton, MO · On-site

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

kindeva

Scientist III

Bridgeton, MO · On-site

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

kindeva

Scientist III

Bridgeton, MO · On-site

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

kindeva

Scientist III

Bridgeton, MO · On-site

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

TekWissen LLC

Analytical Chemist

Chesterfield, MO · On-site

$32/hr

Communicates effectively with diverse customers/stakeholders across R&D, manufacturing, and product supply. POSITION SUMMARY: * We seek an enthusiastic team member with a strong Analytical Chemistry ...

Doe Run

Analytical Chemist

Viburnum, MO · On-site

Conduct method development or test work to improve the accuracy, efficiency, and safety of ... Basic knowledge of analytical lab analysis best practices and processes. * Basic understanding of ...

the Doe Run company

Analytical Chemist

Viburnum, MO · On-site

Conduct method development or test work to improve the accuracy, efficiency, and safety of ... Basic knowledge of analytical lab analysis best practices and processes. * Basic understanding of ...

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Analytical Development information

What are the key skills and qualifications needed to thrive in Analytical Development?

To thrive in Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a relevant degree and experience in analytical methodologies. Familiarity with laboratory instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory guidelines like ICH and GMP, is essential. Strong problem-solving skills, attention to detail, and effective communication set standout professionals apart in this role. These skills ensure the accurate development, validation, and transfer of analytical methods critical for product quality and regulatory compliance.

What is analytical development?

Analytical development is a field within pharmaceutical and biotech industries focused on creating and validating methods to analyze the quality, purity, and potency of drug substances and products. It involves developing techniques such as chromatography and spectroscopy, often requiring knowledge of regulatory standards like GMP and validation processes. Professionals in this area support drug development by ensuring analytical methods are reliable and compliant with industry regulations.

What is the job description of analytical development?

Analytical development involves designing, optimizing, and validating analytical methods to measure the quality and stability of pharmaceutical products. Professionals in this field use techniques such as chromatography and spectroscopy, often working in laboratories under Good Laboratory Practice (GLP) standards. The role requires strong attention to detail, scientific knowledge, and proficiency with laboratory instruments and regulatory guidelines.

What are some common challenges faced in an Analytical Development role, and how can job seekers prepare for them?

Professionals in Analytical Development often encounter challenges such as developing robust methods for complex samples, meeting tight project deadlines, and ensuring regulatory compliance. To prepare, job seekers should build strong problem-solving skills, gain familiarity with a range of analytical techniques (such as HPLC, GC, and spectroscopy), and stay current with industry regulations like ICH guidelines. Collaborating effectively with cross-functional teams, such as Quality Control and Research & Development, is also essential for success in this role.

What is the difference between Analytical Development vs Quality Control Analyst?

AspectAnalytical DevelopmentQuality Control Analyst
Primary FocusDeveloping and optimizing analytical methods for new productsPerforming routine testing to ensure product quality
Work EnvironmentLaboratories involved in method development and validationQuality control labs conducting batch testing and release
Required CredentialsBachelor's or higher in Chemistry, Biochemistry, or related fields; experience in method developmentBachelor's in Chemistry, Biology, or related fields; experience in testing procedures

Analytical Development professionals focus on creating and refining analytical methods for new products, while Quality Control Analysts perform routine testing to verify product quality. Both roles require similar educational backgrounds and work in laboratory settings, but their responsibilities differ in scope and purpose.

What are the most commonly searched types of Analytical Development jobs in Missouri?

The most popular types of Analytical Development jobs in Missouri are:

What are popular job titles related to Analytical Development jobs in Missouri?

For Analytical Development jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Analytical Development jobs in Missouri look for?

The top searched job categories for Analytical Development jobs in Missouri are:

Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Missouri as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Scientist II

Kindeva Drug Delivery

Saint Louis, MO • On-site

Full-time

Posted 13 days ago

Job description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
As an Analytical Development Scientist II, you will play a critical role in supporting analytical method transfer, verification, and validation activities for both small molecule and biologic products within a Contract Development and Manufacturing Organization (CDMO) environment. This position contributes to the development and implementation of analytical capabilities while supporting quality control testing, technical investigations, process transfers, and validation activities. You will collaborate closely with the Manufacturing, Quality, Validation, and Technical Operations teams to ensure analytical activities are executed efficiently and in compliance, in support of bringing life-changing therapies to patients around the world.
Responsibilities
Analytical Method Development, Transfer & Validation
  • Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products.
  • Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, stability samples, and validation studies.
  • Support technical investigations, specification development, regulatory submissions, and analytical activities associated with cleaning validation and manufacturing support.

Laboratory Operations & Continuous Improvement
  • Support the implementation, qualification, and maintenance of analytical instrumentation and laboratory systems.
  • Identify and implement opportunities to improve analytical methods, laboratory processes, efficiency, compliance, and overall testing capabilities.
  • Maintain technical expertise across a variety of analytical and biochemical techniques while supporting laboratory best practices and data integrity requirements.

Cross-Functional Collaboration & Technical Support
  • Collaborate with Quality Control, Manufacturing, Quality Assurance, Validation, and Technical Operations teams to support routine operations and project activities.
  • Provide technical guidance and training to laboratory personnel as needed.
  • Author and revise analytical methods, protocols, reports, Standard Operating Procedures (SOPs), and other technical documentation while maintaining compliance with current Good Manufacturing Practices (cGMPs) and Good Documentation Practices (GDPs).
  • Support occasional off-shift, weekend, or manufacturing-related activities as business needs require.

Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, or a related scientific field with 5+ years of relevant industry experience; Master's degree with 3+ years of relevant industry experience; or Ph.D. with 2+ years of relevant industry experience. Equivalent combinations of education, training, and experience may be considered.
  • Experience supporting Quality Control or Analytical Development activities within GMP-regulated pharmaceutical, biotechnology, or CDMO environments, including biologics (proteins, peptides, monoclonal antibodies) and small molecule pharmaceutical products.
  • Hands-on experience performing analytical method transfer, method validation, compendial verification, troubleshooting, and analytical testing using techniques such as HPLC, UPLC, LC-MS, GC-MS, FTIR, SDS-PAGE, ELISA, Western Blot, protein concentration assays, Karl Fischer titration, pH analysis, and general wet chemistry methods.
  • Proficiency with chromatography data systems and laboratory software platforms, including Empower and Chromeleon, along with a strong understanding of cGMP regulations, FDA and ICH guidance, method validation principles, data integrity requirements, and laboratory safety standards.
  • Demonstrated ability to troubleshoot analytical issues, critically evaluate data, perform statistical calculations, generate technical reports, protocols, SOPs, and other scientific documentation while providing scientifically sound recommendations and conclusions.
  • Strong verbal and written communication skills with the ability to collaborate effectively across cross-functional teams, manage multiple priorities, and meet deadlines in a fast-paced pharmaceutical manufacturing environment.

California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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