quality assurance technical expert (m/f) in loures

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job details

loures, lisboa
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Biotecnologia e Farmacêutica
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job description

Randstad Professionals is specialized in Recruitment and Selection of Middle & Top Management. In partnership with Hovione - a Global Company With more than 55 years of experience in Active Pharmaceutical Ingredients (API) and Development Intermediate Products - we intend to recruit an Quality Assurance Technical Expert.

The QA Technical Expert will be responsible to guarantee cGMP compliance in all activities and systems related to the projects execution, according to Hovione Quality Policy, in quest of continuous improvement of the Quality System efficiency and effectiveness.


• Promote the importance of a continuous improvement culture, mitigating any tendency for complexity;
• Manage Quality Product key activities for the assigned products (Raw Materials, Suppliers, Specifications, Production Processes, Change Control, Deviations, Qualification and Validation, Stability Programs, Batch Release, Equipment Cleaning, Client Audits, Customer Complaints, Customer requirements, PQR) – e.g. approval of operational areas auxiliary documentation, preparation of quality related reports, reviewer of
documentation generated by the operational areas;
• Contribute to the management of the quality system, namely participating in the documentation revision and update;
• Provide training to the operational areas in applicable cGMP and internal procedures;
• Assure and promote compliance on Health, Safety and Environment in the area and activities for which is responsible or in which participates.


• Full time position;
• Social benefits and compensations;
• Excelent work environment, focused in quality and science;
• Career development on quimical, pharma and high technology sector.

If you want to apply for this position upload your CV in Randstad Website and register yourself in the link below (mandatory process).




• University degree in Chemistry, Chemical Engineering, Pharmacy or equivalent degree in a scientific area;
• 2 to 4 years’ experience in Operational areas (RD or Manufacturing);
• Availability to travel abroad to support project’s transfer or implementation;
• cGMP knowledge;
• Regulatory Affairs basic knowledge;
• English fluency (written and oral);
• Ability to stand and to discuss technical aspects with clients and suppliers.