-Managing 100+ digital and non-digital promotional materials in EOS (asset management system) for the Europe, Middle East and Africa regions. -Creation and validation of trainings for new hires and re-training for existing professionals on EOS system and Copy Approval protocols-Working with and actively contributing to cross-functional collaborative groups focused on rollout of business critical projects -Subject matter expert in Copy Approval for US and EMEA regions including but not limited to Regulatory, Medical, HCC, HEMA and Legal protocols

Responsible for the management of creation, updates and changes to digital and non-digital assets, including but not limited to websites, mobile applications, social media platforms and all print materials for the Europe, Middle East and Africa regions.

Responsible for helping with the general management of the copy approval process for advertising and promotional collateral for all of Somerville-Ethicon campus. Monitored job cycles in the electronic workflow tool, EOS. Additional responsibilities included but not limited to:•Worked on multiple projects simultaneously•Established priorities based on workload and customer feedback•Worked independently and handled routine decision-making•Managed expiring items to ensure compliance with Copy Approval process •Maintained on-going partnership with cross-functional stakeholders (Marketing, Professional Education, Sales Learning, HEMA and HCC). •Gained the confidence of project owners and submitters through consistent attention to detail and people skills•Responded to internal and external customer inquiries on projects.•Supported alignment of Somerville and Cincinnati campus to a common Copy Approval Process•Maintained current regulatory and product knowledge•Provided subject matter expertise to customers on new electronic workflow•Pro-actively collaborated with the Compliant Communication technology team to identify and implement technology optimization•Took initiative to propose modifications to procedures and processes as appropriate

Prepare suture and other medical device products for testing according to appropriate protocols and test methodsOperate mechanical testing equipment and other benchtop instrumentation used in the laboratory.Prepare buffer solutions, prepare suture for in-vitro studies and monitor water baths in the in-vitro laboratory. Interface with engineers to coordinate in-vitro studies.Enter sample and test data into electronic databases.Assist with test method validation of suture and other medical devices including: revising or drafting test method procedures, conducting test method validations according to the standard procedure, completing all appropriate paperwork and assisting with approval process. Assist various projects throughout company

Assisted students in improving academic achievement by meeting with them on a regular basis to clarify learning problems and worked on study skills. This also included, reviewing class material, discussing the text, formulating ideas for papers, and working on solutions to problems.

Audit research data against Good Laboratory Practices (GLP). Inspect the facility, research equipment, Training Records. Communicate study status to study director and managementEquipment validation

Prepared laboratory equipment for studiesReviewed study plans/protocolsAdministrative assistanceArchivingStudy report preparation assistance Implant sutures in animal models Necropsy small animals Clinical observations on small animalsPreparation of animals for wet labs