Project Manager

AmbioPharm - A Global Peptide CDMO; Giugliano in Campania; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A global leader in peptide manufacturing is seeking a Project Manager for the Europe region. In this remote role, you will manage documentation and coordinate teams to ensure timely project delivery. The ideal candidate is detail-oriented and bilingual in English and either French or German, with a strong background in chemistry or life sciences. Flexible work arrangements are offered, making this an excellent opportunity to impact the pharmaceutical industry.

Servizi

Flexible work arrangements

Opportunities for growth

Collaborative team environment

Competenze

• Work on multiple projects with minimal supervision.
• Familiarity with CFR 21 and ICH guidelines is desirable.
• Self-motivated and able to work independently.

Mansioni

• Manage complex documentation and coordinate cross-functional teams.
• Monitor project progress and communicate timelines to leadership.
• Facilitate effective meetings and summarize action items.

Conoscenze

Analytical skills

Organizational skills

Interpersonal skills

Communication skills (written and oral)

Proficiency in MS Office

Bilingual in English and French or German

Formazione

BS / BA in chemistry or life science

Strumenti

MS Word

MS Excel

MS Access

MS Outlook

SQL

Descrizione del lavoro

Overview

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

Location: Europe Region (Remote)

Role Overview: We 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.

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.
• Focuses on proactive planning to manage risk, remove barriers, and meet goals.
• Facilitates 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