Project Manager

AmbioPharm - A Global Peptide CDMO; Umbria; Remoto; EUR 45.000 - 65.000; Tempo pieno

Descrizione del lavoro

A global leader in peptide manufacturing is seeking a Project Manager for Europe who is bilingual in English and French or German. The role involves maintaining project files, communicating timelines, and facilitating meetings. Candidates should hold a BS/BA in chemistry or life science, and possess strong analytical and interpersonal skills. Flexible work arrangements are offered, providing opportunities for growth.

Servizi

Flexible work arrangements

Opportunities for growth

Competenze

• Strong analytical and organizational skills.
• Must be fully bilingual in English and French or German.
• Computer skills in MS Word, Excel, Access, Outlook, SQL are required.

Mansioni

• Maintain complex files and document management systems.
• Monitor progress of assigned projects and communicate timelines.
• Facilitate meetings and summarize action items.

Conoscenze

Analytical skills

Organizational skills

Interpersonal skills

Communication skills

Self-motivation

Formazione

BS/BA in chemistry or life science

Strumenti

MS Word

MS Excel

SQL

Descrizione del lavoro

Overview

Project Manager – Europe (Bilingual : English & French or German)

Location: Europe Region (Remote)

Responsibilities

• Maintain complex files and document management systems, and work with project teams to release for company products (drug substance and drug product)
• Maintain organized and accurate record of all product’s specific documents and correspondence with partners, vendors, customers, contract labs, etc.
• Continuously monitor the progress of assigned projects and communicate timelines to senior leadership and executive staff.
• Create and use Gantt charts, spreadsheets, or other appropriate tools to manage projects.
• Focus on proactive planning to manage risk, remove barriers, and meet goals.
• Facilitate meetings and keep them effective by defining concise agenda, acting as a timekeeper, summarizing action items and maintaining records
• Support quality and regulatory affairs when needed. To include, assist in the preparation of the site for customer and agency inspections.
• Facilitate resolution of issues / concerns / problems with internal and external partners.
• Serve as customer liaison between internal departments and customers

Qualifications

• Strong analytical and organizational skills. The successful candidate must be able to work on multiple projects with a minimum of supervision and meet established timelines.
• Qualified candidate should have a BS / BA in chemistry or life science.
• Computer skills in MS Word, Excel, Access, Outlook, SQL, etc. are required.
• Familiarity with both CFR 21 and ICH guidelines in regards to GMPs’ is desirable.
• Must possess strong interpersonal and communication (written and oral) skills.
• Self-motivated, able to work in a team and independently.
• You must be fully bilingual. Fully fluent in English and French or German.

Why Join Us?

• Be part of a globally respected leader in peptide manufacturing
• Work with a passionate and collaborative team
• Make a meaningful impact in the pharmaceutical industry
• Enjoy flexible work arrangements and opportunities for growth