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Process Development Scientist Jobs in Saint Louis, MO

Irca Group

R&D Scientist

Affton, MO

The R&D Scientist will prepare formulations, execute experiments, analyze results, and document ... Demonstrated initiative, adaptability, and a willingness to learn new products, processes, and ...

Irca Group

R&D Scientist

Affton, MO

The R&D Scientist will prepare formulations, execute experiments, analyze results, and document ... Demonstrated initiative, adaptability, and a willingness to learn new products, processes, and ...

Irca Group

R&D Scientist

Affton, MO · On-site

The R&D Scientist will prepare formulations, execute experiments, analyze results, and document ... Demonstrated initiative, adaptability, and a willingness to learn new products, processes, and ...

Kindeva

Analytical Development Scientist II

Bridgeton, MO · On-site

$85 - $120/hr

The Impact You Will Make As an Analytical Development Scientist II, you will play a critical role ... Perform routine and non-routine analytical testing of raw materials, in-process samples, finished ...

Nestle

Scientist Product Development

Saint Louis, MO · On-site

$73K - $103K/yr

As a Scientist, you'll be responsible for supporting the development of new products and processes from concept through commercialization by planning and executing trials, experiments, and technical ...

Eurofins

HPLC Scientist - EMPOWER

Chesterfield, MO · On-site

We are seeking a highly motivated Analytical Scientist to support biotherapeutic process development programs, with a primary focus on large molecule characterization (proteins, polysaccharides ...

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How much do process development scientist jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for process development scientist in Saint Louis, MO is $37.59, according to ZipRecruiter salary data. Most workers in this role earn between $27.60 and $44.86 per hour, depending on experience, location, and employer.

What is a process development scientist?

A Process Development Scientist is a professional who designs, develops, and optimizes processes for manufacturing products, typically in industries like pharmaceuticals, biotechnology, or chemicals. Their work involves scaling up laboratory procedures to full production, improving efficiency, ensuring quality, and meeting regulatory standards. They collaborate with research, engineering, and manufacturing teams to implement new processes or refine existing ones. Process Development Scientists play a critical role in bringing new products from the research phase to commercial production while maintaining safety and compliance.

What are the key skills and qualifications needed to thrive as a process development scientist?

To thrive as a Process Development Scientist, you need a background in chemistry, biochemistry, or chemical engineering, supported by at least a bachelor’s (often master’s or PhD) degree and experience in laboratory research. Familiarity with analytical instrumentation (such as HPLC, GC, and mass spectrometry), process modeling software, and relevant regulatory standards is crucial. Strong problem-solving, collaboration, and communication skills help drive innovation and coordinate with cross-functional teams. These skills ensure the efficient development and scale-up of robust, safe, and cost-effective processes in pharmaceutical, biotech, or chemical manufacturing environments.

What are some typical challenges faced by process development scientists when scaling up from lab experiments to full production?

Process Development Scientists often encounter challenges when transitioning processes from the laboratory to large-scale production. These can include maintaining product quality and consistency, optimizing yields, and ensuring that processes are cost-effective at scale. Addressing equipment differences, process variability, and regulatory compliance are also common hurdles. Collaboration with engineers, manufacturing teams, and quality assurance professionals is essential to successfully navigate these challenges and achieve scalable, robust processes.

What does a process development scientist do?

A process development scientist designs, optimizes, and scales up manufacturing processes for products such as pharmaceuticals or chemicals. They analyze data, troubleshoot issues, and collaborate with cross-functional teams to ensure processes meet quality and regulatory standards, often using tools like statistical analysis and laboratory equipment. Their work supports efficient, reliable production and continuous process improvement.

What are popular job titles related to Process Development Scientist jobs in Saint Louis, MO?

For Process Development Scientist jobs in Saint Louis, MO, the most frequently searched job titles are:

What job categories do people searching Process Development Scientist jobs in Saint Louis, MO look for?

The top searched job categories for Process Development Scientist jobs in Saint Louis, MO are:

Process Development Scientist jobs near you
Infographic showing various Process Development Scientist job openings in Saint Louis, MO as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $78,175 per year, or $37.6 per hour.

Formulation & Process Development Scientist

Bridgeton, MO • On-site

Virbac
See more jobs at Virbacexternal

Full-time

Retirement, PTO

Re-posted 13 days ago

Job description

Experiencing together a unique human adventure
Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business.
Formulation & Process Development Scientist
Virbac Animal Health is seeking a Formulation & Process Scientist to join our team. Virbac is an animal health pharmaceutical company that specializes in dental, medicine, and supplements for dogs, cats, and ferrets in the United States.
The Formulation & Process Development Scientist develops new and optimizes existing Pharmaceutical products for the animal health market and evaluate technologies and/or formulation processes. Provide technical expertise in collaboration with other functional groups to develop and/or optimize products, test new ingredients, and issue material and product specifications.
Experience: BS in Chemistry, Pharmaceutical Science, Chemical Process Engineer or higher degree. 2 to 5 years of experience in a pharmaceutical-related field is desired.
Benefits: 13 Company paid Holidays; 5 personal days (prorated); 15 vacation days (prorated); 5 floating holidays (prorated); 6% 401k match; competitive pay and bonus opportunity; growth opportunities and hybrid schedules based on department and role within the department and much more!
Area of responsibility 1: Development of new pharmaceutical products or optimization of existing pharmaceutical products (R&D roadmap).
Main activities :
  • Lead and manage the development of new drug delivery methods for animals, including creating novel dosage forms and manufacturing processes for both internal and outsourced projects.
  • Create detailed formulation development plans to help establish and meet project timelines.
  • Spearhead the use of Quality by Design (QbD) and Design of Experiments (DOE) to develop products and processes, ensuring product quality by controlling critical factors.
  • Collaborate with the global product development team to prepare, execute, and evaluate the stability of various dosage forms, more specifically solids like tablets and chews, as well as powders and liquids, at lab, pilot, and industrial scales.
  • Identify and resolve issues in manufacturing processes and recommend improvements.
  • Write and approve key documentation, including manufacturing protocols, Master Batch Records, change controls, deviations, and technology transfer reports, for all scale-up or production batches.
  • Mentor and guide product development technicians in data collection and analysis.
  • Compile and analyze stability data.
  • Draft product specifications and organize documentation for the Dossier, collaborating with the analytical and CMC teams.
  • Collaborate closely with manufacturing and operations to monitor production and transfer new products to industrial production.
  • Ensure timely communication about project status, results, and formula/process development to all relevant technical and project teams i.e. Analytical, tech. Reg., QA, API, MSAT, IO.
  • Engage in continuous learning by attending industry expos and conferences, applying acquired knowledg.
  • Maintain compliance with cGMP, GLP, GCP, FDA, and EMA guidelines whenever applicable.
  • Address questions from regulatory authorities and support quality audits.

Expected results:
Ensure products are developed in a timely manner, in agreement with the development plan, and in adherence to applicable regulation requirements.
Ensure the manufacturing process is mastered toward an accurate, robust, and repeatable industrial process.
Area of responsibility 2:
Ensure (maintain/improve) laboratory compliance to GMP/GDP/GCP practices, internal SOPs and safety
Main activities :
  • Ensure data integrity and compliance to company SOPs/policies and specifications, FDA and EMA cGMP regulations, and Virbac safety policy.
  • Maintain a working knowledge of appropriate scientific instrumentation, equipment, and methodologies in manufacturing, packaging and physico-chemical characterization. A
  • Adhere to overall good documentation practices (GDP).
  • Identify and support initiation of Deviations, CAPAs and Investigations.

Expected results: Compliance of the R&D formulation lab to GMP/GDP practices, internal SOPs and safety policy.
Profile
Requirements (Diploma and experience)
BS Chemistry, Pharmaceutical Science, Chemical Process Engineer or higher degree
3+ years of experience in the pharmaceutical-related field.
Skills
This individual has previously demonstrated a high level of Mastery of skills in formulation science and/or process development, project management, in a GMP/GLP environment, either within Virbac or at a previous employer.
Virbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.
Joining Virbac means joining dynamic teams ambitious for success.
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