MANAGER I+D

MCR International; Cataluña; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading chemical multinational in Cataluña seeks a Manager I+D to oversee production support activities and develop new chemical processes. The ideal candidate will have over 5 years in the GMP pharmaceutical sector, excellent leadership skills, and fluency in English and Spanish. Responsibilities include leading technical teams, ensuring quality standards, and managing resources effectively.

Formación

• 5+ years in GMP pharmaceutical and/or chemical industries.
• 1 to 3 years in a similar position.
• Fluent in English and Spanish.

Responsabilidades

• Supervise Production support while ensuring QSE standards.
• Develop and transition new chemical processes to production.
• Manage team and resources to achieve departmental goals.
• Evaluate outsourcing options and process development.

Conocimientos

Leadership

Problem-solving

Organic Chemistry

Process Chemistry

GMP Understanding

Teamwork

Task Organization

Educación

Bachelor’s degree in Chemistry, Pharmacy or Engineering

Master’s degree or PhD

Descripción del empleo

MLF-2511-371

MANAGER I+D

MARESME

Chemical Multinational company, with facilities in el Maresme, is currently looking for a Manager I+D.

Job Mission

Supervise the execution of Production support activities complying with the established planning while ensuring the requested QSE standards. Lead the development of new chemical processes and transfer them to a large-scale production, guaranteeing the highest level of quality and safety, and with a high orientation towards cost efficiency and costumer satisfaction. Define the priority of the experiments according to department and projects timelines. Mentor Development Technicians as well as Operators in their daily work and keep them motivated.

Responsibilities / functions

• Manage team members and material resources to guarantee the achievement of the department.
• Provide and evaluate options for outsourcing, troubleshooting and/or process development.
• Support all QA activities related to Process Development department.
• Lead the design of synthetic processes and purification methods to be able to elaborate active pharmaceutical ingredients or intermediates.
• Coordinate and lead technician’s activities to deliver the result in a timely manner.
• Ensure that equipment is in correct conditions for its use by managing internal and external activities to guarantee the correct calibration / verification / maintenance of the analytical instruments. Verify that available equipment is aligned with required activities or technologies.
• Lead and involve the team into the transfer activities to Production or Quality Control.

Minimum Cualifications

• Bachelor’s degree, master’s degree, or PhD in Chemistry, Pharmacy and/or Engineering.
• More than 5 years in GMP pharmaceutical and/or chemical industries. 1 to 3 years in a similar position.
• Good understanding of GMP requirements, the plant culture and business direction.
• Fluent in English and Spanish
• Must be able to work as part of a team and problem solve independently.
• Excellent knowledge of Organic and/or Process Chemistry.
• Understand the project overview.
• Good leadership capabilities.
• Capacity to organize and prioritize tasks and people considering different projects requirements.
• Mentor team members with his/her knowledge.