PstrongProject Manager – Europe /strong (Bilingual: English French or German) /ppstrongLocation: /strong Europe Region (Remote) /ppbr/ppstrongRole Overview: /strong /ppWe are seeking a detail-oriented and proactive Project Manager to join our European team. This role is pivotal in managing complex documentation, coordinating cross-functional teams, and ensuring timely delivery of projects. You will serve as a key liaison between internal departments and external stakeholders, driving project success through strategic planning and effective communication. /ppbr/ppstrongPrimary Responsibilities: /strong /pulliMaintain complex files and document management systems, and work with project teams to release for company products (drug substance and drug product) /liliMaintain organized and accurate record of all product’s specific documents and correspondence with partners, vendors, customers, contract labs, etc. /liliContinuously monitor the progress of assigned projects and communicate timelines to senior leadership and executive staff. /liliCreate and use Gantt charts, spreadsheets, or other appropriate tools to manage projects. /liliFocuses on proactive planning to manage risk, remove barriers, and meet goals. /liliFacilitates meetings and keep them effective by defining concise agenda, acting as a timekeeper, summarizing action items and maintaining records /liliSupport quality and regulatory affairs when needed. To include, assist in the preparation of the site for customer and agency inspections. /liliFacilitate resolution of issues/concerns/problems with internal and external partners. /liliServe as customer liaison between internal departments and customers /li /ulpstrongQualifications: /strong /pulliStrong analytical and organizational skills. The successful candidate must be able to work on multiple projects with a minimum of supervision and meet established timelines. /liliQualified candidate should have a BS/BA in chemistry or life science. /liliComputer skills in MS Word, Excel, Access, Outlook, SQL, etc. are required. /liliFamiliarity with both CFR 21 and ICH guidelines in regards to GMPs’ is desirable. /liliMust possess strong interpersonal and communication (written and oral) skills. /liliSelf-motivated, able to work in a team and independently. /liliYou must be fully bilingual. Fully fluent in English and French or German. /li /ulpstrongWhy Join Us? /strong /pulliBe part of a globally respected leader in peptide manufacturing /liliWork with a passionate and collaborative team /liliMake a meaningful impact in the pharmaceutical industry /liliEnjoy flexible work arrangements and opportunities for growth /li /ul