Project Manager

We are seeking an experienced Project Manager with a strong background in medical device standards (ISO 13485) and EU MDR compliance to join a cross‑functional engineering environment. This role demands strong leadership, communication, and problem‑solving abilities to drive quality and compliance initiatives.

Responsibilities

Lead and manage multiple projects in compliance with ISO 13485 and EUMDR standards.

Collaborate with cross‑functional teams (CFTs) across engineering, quality, and regulatory functions.

Apply strong analytical skills to interpret data and solve complex problems.

Drive technical excellence, innovation, and continuous improvement.

Communicate effectively across all levels of the organization.

Requirements

Bachelor's degree in mechanical, electronics, or related engineering field (Master's preferred).

59 years of relevant experience, ideally with EUMDR projects.

Proven leadership experience with cross‑functional teams.

Excellent written and verbal communication skills.

Strong organizational and multitasking capabilities.

PMP certification preferred.

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Project Management and Information Technology

Industries

Pharmaceutical Manufacturing

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