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Transforming into digital technology for data management to bring our regulatory compliance into a higher standard of data use and protection, Global Regulatory Affairs CMC & Devices is being ...
Lake county site is preferred but the Hiring manager can consider remote candidates if they’re a good match..Role Name BTS SMO Contract ...
Leads the overall scheduling effort to develop and update schedules for projects under the Technology Transfer Program for active transfers associated with sterile drug product solutions. Ensures ...
Bachelor's Degree or OUR equivalent is required, typically in nursing or scientific field; or R. N. by Associate's Degree with relevant experience is acceptable.Note: These could be LC based ...
Responsible for editing and formatting documents (for example, protocols, investigator brochures, clinical study reports, narratives, etc.) pertaining to medical research to comply with AMA style ...
Perform tasks under the guidance of project lead or CMS departmental principals on analytic design and statistical analytic planning, coordinate real world database management, and data warehouse ...
JOB DESCRIPTION:Medical device experience ideal looking for senior level. Day to day is cyber security procedures and updates on existing SOP DOP procedures. Technically - take care of assessments. ...
As Client is transforming into digital technology for data management to bring our regulatory compliance into a higher standard of data use and protection, Global Regulatory Affairs CMC & Devices ...
We’re looking for an experienced security professional who can apply their experience toward medical device cyber security. Key qualifications: Need someone with experience ...
The resource will primarily be remote however candidate may have to go onsite in Wilmington DE to attend team/dept meetings.Regional Deployment Coordinator for a global manufacturing accounting ...
Candidates will be working remote foreseeable future. Person could remain remote for the duration of the assignment. Running remediation activities in a regulatory affairs Working with 15-20 ...
Remote for now. The overall scope of this position is the Project Management of CMC development, Package development and Pharmaceutical Technical activities in support of new R&D compounds, Life ...
The Automation Engineering (AE) Group is responsible for design, implementation, support, and maintenance of automated engineering solutions in support of site goals and objectives. In such, AE is ...
Years’ Experience: 7+ Skills: Experience with Software as a Medical Device (SaMD). Builds strategic partnerships to further departmental and organizational objectives. Demonstrates ...
The resource will primarily be remote however candidate may have to go onsite in Wilmington DE to attend team/dept meetings.Regional Project Lead for a global manufacturing accounting project, where ...
Can be remote however local to Gaithersburg/ DC area is preferable.The ideal candidate would have strong Project management experience, Procurement experience including but not limited to price/cost ...
Navigational support for developing and driving the GRO TSA exit strategy TSA support for cross functional TSA exit planning, execution and oversight Assist with developing Viatris governance ...
Qualifications Required: Capable of exchanging straightforward information, ask questions, and check for understanding. Must be proficient in Microsoft Office Suite and relevant clinical ...
The incumbent’s primary responsibilities will be the evaluation, coordination, preparation and implementation of pre-market Regulatory Affairs activities. Responsibilities may ...
Job Requirements Basic understanding of MS Windows, Exchange, Windows Client Operating Systems, Group Policy, Active Directory, SMS and group policy based management Evaluate Office 365 ...
