Regional Scheduler/ Metrics Coordinator

Full Time, Temporary/Contract/Project Job Category: Biotech/R&D/Science Relevant Work Experience: 5+ to 7 Years Career Level: Experienced (Non-Manager) Company: Devon Consulting, Clinical Division Email: Apply by Email Reference Code: D8378 Regional Scheduler/ Metrics Coordinator Our client, a world renowned Pharmaceutical and Healthcare company located in Montgomery County, currently has an opening for a Regional Scheduler/Metrics Coordinator. Our client is a billion dollar, international company that offers the opportunity to work with some of the brightest minds in the country and multiple onsite cafeterias! This is an incredible opportunity to join a world leader that can leverage your existing portfolio.Position Summary:This position will be responsible for management of the Global Product Conformance product schedule within the region. Incumbent will work closely with central Analysis and Remediation function to coordinate regional remediation plans for products. This position will support and provide back-up services to Regional Hub Lead. Individual will coordinate key metrics for hub for reporting to GPC Program Management Office.A fluency in written and spoken Spanish is required.Job Responsibilities:- Manage and maintain product schedule within region.- Collaborate with affiliates and plants to ensure implementation and adherence to schedule timelines and adequate consideration of business requirements.- Coordinate remediation plans for region; key point of contact for hub on remediation plans; Interface with central Analysis/Remediation function.- Establish and maintain metrics coordination within regional hub; track and report metrics for all GPC workstreams using dashboards to GPC PMO.- Provide leadership support to Regional Hub Lead; Assume back-up leadership role for hub as needed.- Manage the tracking issues and feedback attained from key customers within region.- Provide updates to Regional Hub Lead and GPC PMO on progress and issues.Required Skills:- Candidates must be bilingual in English/Spanish.- A minimum of a degree level or equivalent qualifications in a life science, chemical or pharmaceutical discipline.- A minimum of five years experience in the pharmaceutical or related industry. - Strong skills in English language (written and oral).- Project planning/coordination/scheduling experience.- Regulatory affairs, GMP, Systems and Process Deployment and appropriate company QSEs.- Understanding of regulatory submission processes and CTD structure. - Attention to detail, right-first-time mentality.- Ability to operate in multi-function environment.- Ability to work effectively within a team.- Good written and verbal communication skills.- Ability to negotiate and be flexible.- Good organization and time management/project management.- Strong desire to achieve optimal results.- Ability to adapt and be flexible.- Good decision making ability.Job Breadth:- Interaction with many different departments within the plant and affiliate. Significant interaction with external customers in Global Regulatory Affairs, Affiliates, and Global Product Conformance team members. Find An IT Job Find A Clinical Job Click here to learn about the benefits provided to Devon Consultants