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Formulation & Process Development Senior Scientist

Job in Bridgeton, St. Louis city, Missouri, 63044, USA
Listing for: Virbac Corporation
Full Time position
Listed on 2026-06-21
Job specializations:
  • Pharmaceutical
  • Healthcare
Salary/Wage Range or Industry Benchmark: 80000 - 110000 USD Yearly USD 80000.00 110000.00 YEAR
Job Description & How to Apply Below
Location: Bridgeton

Job Summary

Virbac Animal Health is seeking a Formulation & Process Senior Scientist to develop new and optimized pharmaceutical products for the animal health market.

Responsibilities
  • Lead and support development of novel dosage forms and manufacturing processes for animals, including tablets, liquids, powders, chews, and sustained‑release products.
  • Prepare formulation development plans, establish project timelines, and manage laboratory, pilot, and industrial scale batches.
  • Apply Quality by Design (QbD) and Design of Experiments (DOE) approaches to identify and control critical process factors.
  • Collaborate with global product development team and conduct stability studies across scales.
  • Prepare and authorize manufacturing protocols, master batch records, change control requests, deviations, and technology transfer reports.
  • Provide guidance to product development technicians and supervise data collection and analysis.
  • Ensure compliance with cGMP, GLP, GCP, FDA, and EMA regulations; support regulatory submissions and audits.
  • Mentor junior formulation scientists, expanding their knowledge & skills.
  • Maintain laboratory compliance with GMP/GDP practices, SOPs, and safety policies; identify and support deviations, CAPAs, and investigations.
Qualifications

Education and Experience

  • BS in Chemistry, Pharmaceutical Science, Chemical Process Engineering or higher degree.
  • 5+ years of experience in a pharmaceutical‑related field.

Skills

  • Expertise in formulation science and/or process development.
  • Strong project management in a GMP/GLP environment.
  • Experience with QbD, DOE, and technology transfer to industrial operations.
  • Knowledge of cGMP, GLP, GCP, FDA, and EMA guidelines.
  • Excellent communication and teamwork skills.
Benefits
  • 13 Company‑paid holidays; 5 personal days; 15 vacation days; 5 floating holidays; all prorated.
  • 6% 401(k) match.
  • Competitive pay and bonus opportunity.
  • Growth opportunities within the department and beyond.
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Position Requirements
10+ Years work experience
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