Head of Analytical & Manufacturing Science

Job Grade: TEC13 

Hiring Manager: Hedinn Valthorsson 

​Empleado  |  Permanente  |  A tiempo completo  |  In situ​

Nuestro personal de Manufacturing & Global Operations comparte dos prioridades: lograr que las cosas pasen y hacer que cada vez sean mejores. Si eres una persona dinámica y con una mentalidad positiva, encajarás muy bien aquí. Somos un equipo multicultural con un gran espíritu de colaboración. Juntos, nos aseguramos de que nuestros productos cumplan con los más altos estándares de calidad mediante la búsqueda constante de formas de mejorar en cada etapa de nuestra cadena de valor, desde las materias primas que compramos hasta la red logística que lleva nuestros medicamentos a los pacientes. Únete a nuestro equipo y ayúdanos a hacer una contribución aún mayor al futuro de Grünenthal.

What is the job like

Every day you will enjoy different challenges such as:

•Directing and executing the program for the development and validation of analytical methods and manufacturing processes for products made by Tecnandina and/or third parties.

•Communicating and reporting to headquarters on implementation strategies for development projects, formulation processes, and pharmaceutical product transfers.

•Applying QBD, troubleshooting, and GMP tools in the development and transfer of pharmaceutical products.

•Organizing, planning, and reviewing the processes and documents for the different analytical activities.

•Monitor and evaluate the performance of the analysts under your supervision and the completion of tasks to ensure that objectives are met.

•Plan and coordinate with the relevant departments the instrumental requirements for the daily execution of validation, approval, and development analyses.

•Develop the master plan for transfer, development, and approval projects, their maintenance, and compliance.

Your contribution

To make the most for this role, you must have:

•5-8years of experience in pharmaceutical industry laboratories (or similar) and various analytical processes, development of analytical methodologies, stability studies, manufacturing process validations, and analytical methods.

•At least 1 year of experience in leadership

•Experience in improvement and optimization processes.

•Experience in experimental design and statistics.

•Experience working under quality, QBD, GMP, GLD, GDP, and safety standards.

•Higher education in Biochemistry and Pharmacy, Chemical Engineering, Biotechnology, and/or related fields.

•Advanced level of English.

•Experience in planning, executing, and supervising activities related to development projects.

•Ability to organize activities and work teams.