20 Katalyst Jobs Hiring in Georgia

RESPONSIBILITIES * The following duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all-inclusive. * The omission of ...

The role of the Senior Quality Control Specialist is to provide technical expertise and support for the Operational Support functions of the QC Laboratory. Responsibilities: * Perform compendial ...

Responsibilities: * This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product ...

Responsibilities: * Support the Senior Director in developing and executing regional regulatory strategies for QOL * initiatives within specific regions. * Contribute to providing strategic oversight ...

Requirements: * B.Sc., M.Sc., or equivalent education in Biostatistics/Statistics, Bioinformatics, Life Sciences, Mathematics, Physical Sciences, or related fields * Advanced SAS macro programming ...

Responsibilities: * This position is responsible for developing and implementing global CMC regulatory strategies. * The role involves coordinating CMC regulatory activities to support the clinical ...

Responsibilities: * Maintain and update EDC user access across multiple clinical studies * Track and manage user access requests in coordination with CRAs and EDC vendors * Curate and maintain ...

Responsibilities: * In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ...

* This position is Non-exempt. Hours over 40 will be paid at Time and a Half. * The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product ...

Roles & Responsibilities: * Independently draft and execute complex validation plans, protocols, and test strategies to ensure compliance and expedited release of critical site equipment. * Balance ...

* The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. * Responsible for maintaining a strong collaborative ...

Responsibilities: * Lead the preparation, review, and submission of CMC sections of regulatory filings (e.g., INDs, NDAs, BLAs, MAAs, variations, renewals) to global health authorities, ensuring ...

Responsibilities: * This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product ...

* The Sr. Product Quality Engineer will serve as a technical representative providing design quality expertise to a product development team. * Responsible for maintaining a strong collaborative ...

Responsibilities: * Lead CDM activities for assigned clinical studies, ensuring data quality and compliance with study timelines. * Design and/or support the design of clinical databases in alignment ...

Responsibilities: * Lead clinical data management activities for pivotal trials in a dynamic environment. * Collaborate with cross-functional teams to ensure high-quality data deliverables. * Drive ...

Responsibilities: * Develop accurate, professional engineering drawings from redlines and design schematics. * Coordinate CAD work with engineers, designers, and CAD drafters to meet project ...

Responsibilities: * In this critical role, you will lead regulatory strategies, product submissions, and a team of talented regulatory affairs professionals to drive timely product approvals and ...

Job Summary: We are seeking a highly experienced Staff Process Development Engineer to lead manufacturing process development activities supporting new product development (NPD), product design ...

Responsibilities: * This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product ...