Virbac Jobs Hiring Now
Virbac is hiring for 9 open roles on Migrate Mate as of July 16, 2026, concentrated in manufacturing operations and engineering (Non-Software). Migrate Mate updates Virbac's live openings daily. Virbac is an animal health company that develops and manufactures pharmaceutical and biological products for companion animals and livestock.
Find Virbac JobsOverview
Virbac hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 9
- Top team
- Manufacturing Operations
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Bridgeton
Open Roles at Virbac
Showing 9 of 9+ Virbac jobs
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.
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.
Job Roles at Virbac
Working at Virbac
Virbac's 9 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are manufacturing operations, engineering (Non-Software), and account management. Virbac is an animal health company focused on developing, manufacturing, and commercializing pharmaceutical and biological products for veterinary use. Its operations span production, quality assurance, scientific research, sales, and finance across U.S. facilities. Most Virbac roles are based in Bridgeton and Westlake.
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Browse jobs by roleVirbac Jobs: Frequently Asked Questions
How many jobs is Virbac hiring for right now?
Virbac is hiring for 9 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in manufacturing operations and engineering (Non-Software). Roles span pharmaceutical manufacturing, quality assurance, engineering, finance, and sales. Migrate Mate pulls Virbac's current openings continuously, so the count reflects what is actively posted.
What kinds of roles does Virbac hire for?
The most active teams are manufacturing operations, engineering (Non-Software), and account management. Virbac's postings cover pharmaceutical production, quality assurance, formulation and process development, packaging engineering, plant finance, IT systems, and territory sales. Most postings are across all levels, with a mix of hands-on manufacturing roles and professional or specialist positions in science, finance, and technology.
Are Virbac jobs remote or in-person?
Mostly on-site. About 0% of Virbac's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Bridgeton. Each Virbac listing shows its work location so you can filter before applying.
How do I apply to a job at Virbac?
Find a Virbac role on Migrate Mate and follow the listing through to Virbac's own careers page to submit your application. Virbac manages its own hiring process, including application review and interviews. Migrate Mate keeps Virbac's listings current so you can find and track openings without missing a posting.
Does Virbac hire entry-level?
Most of Virbac's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Virbac listings for stated experience requirements.
Where is Virbac hiring?
Most Virbac roles are based in Bridgeton and Westlake, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.