Formulation & Process Development Senior Scientist

Location: Bridgeton

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.

Virbac Animal Health is seeking a Formulation & Process Senior Scientist to join our team. The Formulation & Process Development Senior Scientist develops new and optimized existing pharmaceutical products for the animal health market. Identify and evaluate new technologies and/or formulation processes Provide technical expertise in collaboration with other functional groups to prepare formulations development plans, to help establish and meet project timelines, prepare laboratory, pilot, and industrial scale batches, and support technology transfer to Industrial operations, for a variety of product dosage forms including, tablets, liquids, powders, chews and others, in compliance with cGMP, FDA and EMA regulations/guidelines.

Mentor the Junior Formulation Scientists.

Experience:

BS in Chemistry, Pharmaceutical Science, Chemical Process Engineer or higher degree. 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 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 support the development of novel dosage forms and manufacturing processes for the delivery of drugs to animals, for internal and subcontracted projects i.e. CMOs.

* Prepare formulation development plans to help establish and meet project timelines.

* Lead The Quality by Design (QbD) and Design of Experiments (DOE) approach to develop products and processes that helps identify and control critical factors that affect product quality.

* Collaborate with the global product development team to prepare, execute, and evaluate the stability of laboratory-scale, pilot and industrial scale-up batches, to test a variety of product dosage forms including tablets, liquids, powders, soft chews, sustained-release products and others.

* Troubleshoot problem processes and suggest improvements to manufacturing Prepare and authorize manufacturing protocols, Master batch records, change control requests, deviations, development and technology transfer reports, for all scale-up or production batches.

* Provide guidance to the product development technicians in data collection and analysis.

* Evaluate and compile stability data.

* Prepare product specifications and assemble documentation to support the part II of the Dossier, in collaboration with the analytical and CMC teams.

* Work closely with manufacturing and operations teams, monitoring production runs, and ultimately, transfer of new products to industrial production. Communicate effectively in a timely manner and within a team setting, all information regarding formula and processes development, project status, results, across technical departments and the global project team i.e. Analytical, tech. Reg., QA, API, MSAT/IO etc.

* Engage in continuous learning by attending industry expos and conferences, applying acquired knowledge.

* Adhere to cGMP, GLP, GCP, FDA and EMA legislations and guidelines, whenever applicable.

* Ensure answers to questions from the authorities evaluating AMM files and quality/audits…