in Pharmacy, Chemistry, Pharmaceutical Sciences, or related scientific discipline. 5-7 years of experience in regulatory affairs...
Job description: The Biologics CMC Developability (BCD) group sits at the interface of discovery and development. The core role of BCD is to deliver meaningful and actionable data to support the selection of candidate molecules to progress...
Job Description: The Quantitative, Translational ADME Sciences (QTAS) department at client is seeking a highly...
clinical development life cycle Compile, coordinate and review applications to Regulatory Authorities including...
, and system life cycle documentation. Staying aligned with the project schedule and escalating risks or roadblocks early...
in lifesciences, health informatics, computer science, or related field. Advanced degree preferred. Strong understanding...
Responsibilities: Reporting to the Clinical Data Manager, you'll be responsible for the development of real-world data variables from structured and unstructured data sources, including designing data capture forms and supplemental proced...
Summary : The Supplier Quality engineer will work closely with our suppliers and purchasing group to resolve supplier issues and prevent their reoccurrence. Applies and maintains standards for manufacturing, quality, design, testing, and i...
Job Description: Performs physical and/or administrative tasks involved in the shipping, receiving, storing, distributing and order fulfillment of merchandise, products, materials, parts, supplies and equipment. Checks goods received and f...
Job Description: Performs both production assembly operations and complete system analysis, testing and performance optimization. Performs basic electrical, mechanical or software troubleshooting to determine problems in non-functioning te...