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Formulation Development Cmc Jobs in Kansas (NOW HIRING)

Formulation Development Cmc information

What is the role of CMC in drug development?

In formulation development, CMC (Chemistry, Manufacturing, and Controls) ensures the quality, safety, and efficacy of a drug by establishing manufacturing processes, quality standards, and regulatory documentation. Formulation scientists and CMC teams collaborate to develop stable, scalable drug products that meet regulatory requirements throughout development and commercialization.

What is the salary of formulation R&D?

The salary for a Formulation Development CMC professional typically ranges from $70,000 to $130,000 annually, depending on experience, education, and location. Entry-level roles may start lower, while senior positions with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Research and Development or Chief Scientific Officer typically have the highest salaries, often exceeding several hundred thousand dollars annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company innovation.

What is the difference between Formulation Development Cmc vs Formulation Scientist?

AspectFormulation Development CmcFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; industry certificationsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing settingsResearch labs, development facilities, pharmaceutical companies
Industry UsageRegulatory submissions, product development, manufacturing supportFormulation research, experimental design, product optimization

Formulation Development Cmc focuses on developing formulations suitable for regulatory approval and manufacturing, often involving documentation and compliance. Formulation Scientists primarily conduct research and experiments to create and optimize formulations. While both roles require similar educational backgrounds and work in related environments, Cmc roles emphasize regulatory and manufacturing aspects, whereas Scientists focus on experimental research and innovation.

Is formulation part of CMC?

In formulation development roles within CMC (Chemistry, Manufacturing, and Controls), formulation is a core component, involving the design and optimization of drug formulations to ensure stability, efficacy, and manufacturability. These professionals work with analytical tools, quality standards, and regulatory requirements to develop suitable formulations for clinical and commercial products.

What is Formulation Development CMC?

Formulation Development CMC (Chemistry, Manufacturing, and Controls) refers to the process of designing and optimizing the composition of a drug product, ensuring it is safe, effective, and stable for patient use. This role involves selecting appropriate excipients, developing the manufacturing process, and generating the data required to support regulatory submissions. CMC professionals collaborate with research, quality, and regulatory teams to ensure that the drug product meets all necessary standards throughout its lifecycle.

What are the key skills and qualifications needed to thrive as a Formulation Development CMC specialist, and why are they important?

To thrive as a Formulation Development CMC specialist, you need expertise in pharmaceutical sciences, chemistry, and regulatory guidelines, often supported by an advanced degree in a relevant field. Familiarity with analytical techniques, formulation equipment, and regulatory submission systems like eCTD is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the successful development, optimization, and regulatory approval of safe and effective pharmaceutical products.

What are some typical challenges faced by professionals in Formulation Development CMC, and how are they addressed?

Professionals in Formulation Development CMC often encounter challenges such as ensuring formulation stability, meeting regulatory requirements, and scaling up from laboratory to manufacturing. Addressing these challenges requires close collaboration with analytical, regulatory, and manufacturing teams, as well as staying current with evolving guidelines. Effective project management, rigorous experimental design, and proactive risk assessment are key strategies to successfully navigate these complexities and ensure timely progress of drug development projects.
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Infographic showing various Formulation Development Cmc job openings in Kansas as of July 2026, with employment types broken down into 46% Internship, 1% As Needed, 46% Full Time, 4% Part Time, 1% Contract, and 2% Summer. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.
Scientist I/Analytical Chemist

Full-time

Posted 18 days ago


Job description

SUMMARY

This position is responsible for support of CMC activities as well as working with Scientists and management for specific compound development at CritiTech in support of CritiTech product development and associated affiliates/partners for the global development and regulatory approval of New Chemical Entities (NCE’s), Active Pharmaceutical Ingredients (APIs) and support of research and development of any/all product activities.

RESPONSIBILITIES

  • Participates in lab development in support of Chemistry, Manufacturing and Controls (CMC) section of NDA or SNDA by direction and interaction with Quality Operations/Regulatory Affairs and CritiTech.
  • Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech’s Supercritical Precipitation equipment.
  • Provides analytical support for proof of concept studies, feasibility studies, routine manufacturing, and troubleshooting using CritiTech’s spray drying equipment.
  • Perform production activities in support of clinical trials, including filling, environmental monitoring, visual inspection, and packaging of vials for further processing.
  • Suggest changes and improvements to CritiTech’s analytical services and product characterization, facilities, utilities, and other systems.
  • Performs preventative maintenance and calibration checks on analytical equipment.
  • Participates in the qualification of new equipment and facilities.
  • Generates support data for CritiTech to be used in 3rd party development activities.
  • Generates data in support of CMC documents, including out-of-specification (OOS) or deviation investigations, and helps execute action plans to meet sound scientific practices.
  • Provides technical support for QO on complaint samples and manufacturing/packaging problems.
  • Performs and assists in CritiTech compatibility and feasibility assessments for compounds being considered for development.
  • Participate in the onsite review of data, facilities and laboratory operations of contract manufacturing and analytical laboratory.
  • Suggests changes or edits to appropriate SOP’s for CritiTech.
  • Performs release and stability analytical testing with QO in the coordination and management of retest/expiration dating.
  • Executes testing and lab work in support of technology transfer and stability protocols, stability packaging and manufacturing jobs for CritiTech activities.
  • Other duties as assigned.

EDUCATION, EXPERIENCE AND SKILLS

Required

  • BS in chemistry, biology, engineering or related pharmaceutical field with 3+ years industry background in pharmaceutical product development – or –
  • MS in chemistry, biology, engineering or related pharmaceutical field with 2+ years industry background in pharmaceutical product development.
  • 2+ years preparing and supporting CMC documentation for IND’s and NDA’s.
  • Experience in working with people in a multi-disciplinary team environment.

Preferred

  • Advanced degree in chemistry or pharmacy or equivalent experience.
  • Experience in pharmaceutics, analytical and organic chemistry.
  • Experience in technology transfers to contract facilities.
  • Experience with interactions with regulatory agencies.
  • Experience in preparing and supporting Chemistry, Manufacturing and Control (CMC) documentation regulatory filings.

KNOWLEDGE AND SKILLS

  • Knowledgeable (including hands-on experience) in the use of analytical methods for active pharmaceutical ingredients and drug product (i.e. HPLC, GC, IR, etc.) and formulation development/manufacturing and the relation of these to overall pharmaceutical development.
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) as well as other pertinent national regulations.
  • Current knowledge of CMC regulatory and ICH guidelines.
  • Knowledgeable in the overall drug development process.
  • Knowledgeable in the application of compendia requirements and procedures to testing and developing pharmaceutical products.
  • Leadership Skills - knowledge and interpersonal skills to help others towards the accomplishment of CritiTech’s goals and objectives.
  • Analytical and Problem-Solving Skills - ability to identify problems or opportunities using appropriate information; determines the causes and possible solutions to the problem.
  • Teamwork - the ability to work well and manage personnel in a highly cross-functional team environment.
  • Communication Skills – ability to express one’s self clearly and concisely to CritiTech personnel over the phone or with others within the team; documents issues and/or concerns concisely and comprehensively; adjusts language and/or terminology appropriate for the audience.
  • Interpersonal Flexibility – ability to adapt to other personalities in a respectful manner that is conducive to goal achievement.
  • Knowledge Sharing – ability to capture knowledge within the organization; improves solutions, processes, an deliverables through the use of information; improves information capital by contributing experience, theories, deliverables, and models for others to use.
  • Resource Management – ability to work with internal and external resources and to coordinate individual goals and objectives to align with business imperatives.