Project Manager

AmbioPharm - A Global Peptide CDMO; Latina; Remoto; EUR 60.000 - 80.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is hiring a Project Manager to oversee projects across Europe. The role requires strong analytical and organizational skills, with a focus on managing timelines and liaising with customers. Candidates must be bilingual in English and French or German, and possess a BS/BA in chemistry or life science. Join a respected leader in peptide manufacturing and enjoy flexible work arrangements and growth opportunities.

Servizi

Flexible work arrangements

Opportunities for growth

Competenze

• Work on multiple projects with minimal supervision and meet timelines.
• Familiarity with CFR 21 and ICH guidelines regarding GMPs is desirable.
• Strong oral and written communication skills.

Mansioni

• Maintain complex files and document management systems.
• Monitor project progress and communicate timelines.
• Facilitate meetings and define clear agendas.

Conoscenze

Analytical skills

Organizational skills

Interpersonal communication

Project management

Bilingual in English and French or German

Formazione

BS/BA in chemistry or life science

Strumenti

MS Word

Excel

Access

Outlook

SQL

Descrizione del lavoro

Overview

Project Manager – Europe. Bilingual: English and 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 agendas, acting as a timekeeper, summarizing action items and maintaining records.
• Support quality and regulatory affairs when needed, including assisting 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.
• BS/BA in chemistry or life science.
• Computer skills in MS Word, Excel, Access, Outlook, SQL, etc.
• Familiarity with CFR 21 and ICH guidelines regarding GMPs is desirable.
• Strong interpersonal and communication (written and oral) skills.
• Self-motivated, able to work in a team and independently.
• Fully bilingual 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.