Join our Pharma Services team and be a part of a leading contract development and manufacturing organization (CDMO) offering end-to-end services for drug development, clinical trial logistics, and commercial manufacturing! Biotech and biopharma companies trust us for our speed, flexibility, and quality across every phase of drug development. With worldwide locations, we support active pharmaceutical ingredients (APIs), biologics, cell therapy, viral vectors, formulation, clinical trials, logistics, commercial manufacturing, and packaging. Help us enable many major therapies on the market today and drive the future of healthcare! DESCRIPTION: How will you make an impact By executing key deliverables for the implementation of a practical, proactive, sustainable, scalable, and effective Quality Risk Management Program within the Pharma Services Group. Must be highly organized with an ability to multi-task, work and communicate across multiple sites, different business units, and functions, encompassing the full product life cycle, from early product & process development through commercial manufacturing. Will assist in developing and deploying global processes and systems that must effectively work for multiple sites and will ensure and facilitate their adoption while using industry standard methodologies and body of knowledge and, incorporating different requirements and expectations from various regulatory bodies. The position will be in the Global Quality Systems – Quality Operations Team and will report to the Director of Quality Risk Management.
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Job Type
Full-time
Career Level
Manager
Number of Employees
5,001-10,000 employees