Project Manager

AmbioPharm - A Global Peptide CDMO · Rovigo, Italia ·


Descrizione dell'offerta

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.


Primary 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

Candidatura e Ritorno (in fondo)