Project Manager (In vitro diagnostic)

Randstad España; Barcelona; Presencial; EUR 50.000 - 70.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Stable project in leading company

Attractive compensation package

Descripción de la vacante

Randstad España is searching for a Project Manager to lead various projects aimed at enhancing quality and introducing new products within a prominent biotechnology company in Barcelona.

The successful candidate will manage project delivery, interact with suppliers, and ensure compliance with regulatory frameworks, particularly in In Vitro Diagnostics development.

The position offers an attractive compensation package and the chance to work in a stable project environment.

Formación

• Proven experience in IVD (In Vitro Diagnostics) development.
• Deep understanding of regulatory framework (IVDR and FDA).
• Familiarity with 21CFR820, GMP, ISO 13485.

Responsabilidades

• Plans and manages projects through to completion.
• Prepares reports and delivers presentations.
• Interacts with and manages suppliers.

Conocimientos

Project management

Supplier management

Advanced English

Educación

Bachelor's or Master's degree in Biotechnology or related field

Descripción del empleo

An important biotechnology company located in Barcelona is looking to recruit a Project Manager.

This role involves developing projects aimed at improving quality, introducing new products, and validating processes to ensure product quality is maintained.

Responsibilities

• Plans and manages projects through to completion, defining resource requirements, identifying key resources, and influencing others to deliver projects on time and within budget.
• Prepares reports, publishes, and delivers presentations to communicate findings.
• Interacts with and manages suppliers.

Requirements

• Bachelor’s or Master’s degree in Biotechnology, Bioengineering, or a related field.
• Advanced level of English.
• Proven experience in IVD (In Vitro Diagnostics) development, including a deep understanding of the regulatory framework (IVDR and FDA).
• Familiarity with 21CFR820, GMP, ISO 13485, ISO 9001 series, and national/international regulations and standards related to the medical device industry.

We offer

• Stable project in a leading company within its sector.
• Attractive compensation package.