Mf01-021224 Project Manager - New Products

Veg Group; Comunidad Valenciana; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

Una empresa líder en servicios busca un individuo talentoso y dedicado para unirse a su equipo. Este puesto implica trabajar con los más altos estándares éticos en la industria farmacéutica, de dispositivos médicos y biotecnología. El candidato ideal debe tener una licenciatura en ciencias o ingeniería, así como una sólida experiencia en áreas de proceso y fabricación. La posición requiere habilidades de comunicación excepcionales en inglés y español, junto con un profundo conocimiento de las regulaciones cGxP. Si tienes pasión por la calidad y el cumplimiento, esta es una gran oportunidad para hacer una diferencia significativa en un entorno dinámico y colaborativo.

Formación

• 5+ años de experiencia en industrias farmacéuticas o de dispositivos médicos.
• Conocimiento fuerte en cGxP y regulaciones aplicables.

Responsabilidades

• Crear planes a corto y largo plazo, incluyendo objetivos y plazos.
• Delegar tareas en el proyecto a los empleados adecuados.

Conocimientos

Bilingüe (Inglés/Español)

Conocimientos en cGxP

Habilidades de redacción técnica

Gestión de riesgos

Educación

Licenciatura en Ciencias o Ingeniería

Descripción del empleo

Career Opportunities with Validation & Engineering Group

A great place to work.

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Qualifications:

• Bachelor's Degree in Science or Engineering.
• Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
• Experience in direct process/manufacturing areas.
• Must be fully bilingual (English/Spanish) with excellent oral skills.
• Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
• Strong knowledge (according to related area).
• Technical writing skills and investigations processes.
• Available to work extended hours, with the possibility of weekends and holidays.

Responsibilities:

• Creating long- and short-term plans, including setting targets for milestones, adhering to deadlines, and allocating resources.
• Delegating tasks on the project to employees best positioned to complete them.
• Identifying and managing potential risks and liabilities of multiple projects.
• Assisting in the definition of project scope and goals.
• Making effective decisions when presented with multiple options for how to progress with the project.
• Serving as a point of contact for teams when multiple units are assigned to the same project to ensure team actions remain in synergy.
• Communicating with executives or the board to keep the project aligned with their goals.
• Performing quality control on the project throughout development to maintain the standards expected.
• Adjusting schedules and targets on the project as needed.
• Motivating people involved in the project to complete tasks on time.