Viatris Pharmaceuticals LLC is seeking a QA Technical Support/Compliance Specialist with a strong background in the pharmaceutical industry to perform quality control tasks including sampling, testing, and compliance with regulatory standards. The ideal candidate will have at least five years of relevant experience, a bachelor's degree in a related field, and be fully bilingual in English and Spanish
Job Summary
Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally.
The Technical Specialist role involves performing sampling, testing, technical support, equipment validation, and regulatory compliance to ensure quality control in pharmaceutical manufacturing.
Viatris offers competitive salaries, benefits, and an inclusive environment where employees can use their experiences, perspectives, and skills to make an impact on the lives of others.
Matching Summary
Match Score: 85
Viatris Pharmaceuticals LLC is seeking a QA Technical Support/Compliance Specialist with a strong background in the pharmaceutical industry to perform quality control tasks including sampling, testing, and compliance with regulatory standards. The ideal candidate will have at least five years of relevant experience, a bachelor's degree in a related field, and be fully bilingual in English and Spanish.
Skills & Requirements
Must-have
sampling for testing incoming materials
technical support in QC laboratories
knowledge of GMP and validation principles
regulatory documentation review and approval
equipment calibration and validation
proficient in Microsoft Office
bilingual English and Spanish
Nice-to-have
process improvement opportunities
training on new systems and techniques
liaison between technical development and QC
working weekends and after hours
Key Requirements
Bachelor’s degree in pharmacy, chemistry, natural science, engineering or related
At least five years pharmaceutical industry experience
Knowledge of NDA, CMC, DEA/FDA regulations
Familiarity with compendial methodologies USP, EP, JP, CH