Project Manager

AmbioPharm - A Global Peptide CDMO; Monza; Remoto; EUR 50.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading peptide manufacturing company is seeking a Project Manager for Europe, who will handle document management and project oversight. The ideal candidate must be fully bilingual in English and either French or German, possess a degree in life sciences, and demonstrate strong analytical skills. Enjoy flexible work arrangements and be a part of an impactful team in the pharmaceutical industry.

Servizi

Flexible work arrangements

Opportunities for growth

Collaborative team environment

Competenze

• Strong analytical and organizational skills; able to manage multiple projects.
• Requires a BS/BA in chemistry or life sciences.
• Fluency in English and French or German is mandatory.

Mansioni

• Maintain files and document management systems for products.
• Monitor project progress and communicate timelines to leadership.
• Facilitate meetings and keep effective records.

Conoscenze

Strong analytical skills

Organizational skills

Bilingual in English and French or German

Interpersonal skills

Communication skills

Self-motivated

Formazione

BS/BA in chemistry or life science

Strumenti

MS Word

Excel

Access

Outlook

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.
• 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