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Careers

We acknowledge the importance of people. Only by developping and selecting the human potential of the organization we can undertake the challenges that the future reserves us. 

The growing of a company feeds of everybody's effort, of the continued training of our professionals and of the support of its personal needs. For this reason, we make the staff's wellness our fundamental pillar of our entrepreneurial approach.  

All of this makes Progenie Molecular a company with scarce staff rotation, with a pleasant working environment and integrated by great professionals and people.

Biomedicine Commercial Engineer (MADRID)

Profile:

- Postgraduate in Health Sciences
- Commercial experience in medical visit or similar
-Resident in Madrid or in the surrounding area

Responsabilities:

- Marketing of diagnostic services and products of the company
- Technical assistance and maintenance of the current customers' portfolio
- Budget preparation
- Collaboration and elaboration of the marketing plan

Additional requirements:

- Knowledge of the diagnostic field
- Flexiblility to travel frequently
- Intermediate-advanced English profiency  
Biomedicine Commercial Engineer (MALAGA)

Profile:

- Postgraduate in Health Sciences
- Commercial experience in medical visit or similar
-Resident in Malaga or in the surrounding area

Responsabilities:

- Marketing of diagnostic services and products of the company
- Technical assistance and maintenance of the current customers' portfolio
- Budget preparation
- Collaboration and elaboration of the marketing plan

Additional requirements:

- Knowledge of the diagnostic field
- Flexiblility to travel frequently
- Intermediate-advanced English profiency  
Quality Engineer

Profile:

- Grade in Health Sciences (preferable)
- Experience in implementation and management of quality systems (essential)

Responsabilities:

- Be integrated into the quality and documentation department
- Tasks related to the transiction from ISO 9001:2008 to ISO 9001:2015
- Preparation of the technical documentation (manuals, safety sheets, etc)

Additional requirements:

- Previous experience in ISO 13485:2003 e ISO 15189:2013
- Previous experience in GLPs in clinical laboratories
- Intermediate-advanced English profiency