Project Manager

AmbioPharm - A Global Peptide CDMO; Barazzetto; Remoto; EUR 55.000 - 75.000; Tempo pieno

Descrizione del lavoro

A leading global CDMO is seeking a Project Manager to oversee complex projects and maintain documentation. The ideal candidate will have a Bachelor's in chemistry or life science, strong communication skills, and be fully bilingual in English and either French or German. This role offers flexibility and growth opportunities while contributing to impactful work in the pharmaceutical industry.

Servizi

Flexible work arrangements

Opportunities for growth

Collaborative team environment

Competenze

• Ability to work on multiple projects with minimal supervision.
• Familiarity with CFR 21 and ICH guidelines regarding GMPs is desirable.
• Self-motivated and able to work in a team and independently.

Mansioni

• Maintain files and document management systems for products.
• Monitor progress of projects and communicate timelines.
• Facilitate meetings and keep them effective.
• Serve as customer liaison between internal departments and customers.

Conoscenze

Analytical skills

Organizational skills

Communication skills

Fluency in English

Fluency in French or German

Formazione

Bachelor's degree in chemistry or life science

Strumenti

MS Word

MS Excel

MS Access

MS Outlook

SQL

Descrizione del lavoro

Overview

Project Manager – Europe

Location: Europe Region (Remote). Bilingual: English & French or German.

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, 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; ability to work on multiple projects with minimal supervision and meet established timelines.
• Bachelor's degree 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; 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.