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The Sr. Manager, Facilities Compliance will be responsible for site compliance for the Facilities Department. Responsibilities include ensuring completeness of documentation and support to the identification and management of deviations, CAPA, and other quality events associated with Facilities, as required. Reporting to Sr. Director, MSAT & External Manufacturing Locatio
Posted 4 days ago
The Professional Aesthetic Consultant (PAC) promotes the product portfolio to targeted aesthetic customers within a designated geographical area. This role will create product acceptance and enhance portfolio growth through various business development activities. The PAC provides technical product and procedure expertise. Reporting to Regional Sales Manager Location/Terr
Posted 4 days ago
The Lead, Regulatory Operations is responsible for managing Regulatory Affairs activities (nonclinical, clinical and CMC) for assigned investigational development products from preclinical candidate designation through product approval, including regulatory submissions. This individual is responsible for maintaining an in depth awareness of relevant federal and internatio
Posted 4 days ago
The QC Analyst II Cell Based Potency Assay will support finished product testing with focus on laboratory organization, testing coordination, and execution of a cell based potency assay for Botulinum toxin within a Quality Control environment. Reviews laboratory documentation for accuracy and perform routine laboratory duties. Supports team members to meet group goals. Pa
Posted 9 days ago
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