Quality Assurance Consultant Job Description and Duties

Job Description and Duties

To this end, you are in charge of:

Improve quality: anticipate drifts and malfunctions, implement corrective and preventive actions (CAPA);

Manage deviations: conduct investigations following deviations and ensure communication with the client;

Prepare internal and external audits, supplier audits;

Track change requests and OOS;

Participate in the monitoring of batches, in the process of resolving discrepancies following non-conformities or audits;

Track self-inspections;

Manage milestones/indicators on the Operational Quality side;

Coordinate and monitor Change Controls and approve operational documents related to processes;

Ensure the monitoring of the evolution of the Quality Assurance system of the domain entrusted in accordance with the Quality policy of the site, and the standards in force (BPF, GMP, Public Health Code, ISO standards, etc.);

Advise and propose corrective actions, support the implementation and optimization of quality management systems

Evolve within a specialized company, with collaborators passionate about innovation in biotechnology and pharmacology.

Integrate a human-sized SME (85 employees) where team spirit, local management and conviviality are experienced on a daily basis.

Have the opportunity to work on projects with high added value within large pharmaceutical and cosmetic laboratories but also SMEs and start-ups specializing in biotechnology.

The raison d’être of Pharmacos? Respond in an innovative way to the needs of life sciences companies. Created in 2007, present in France, Europe and internationally, PHARMACOS supports pharmaceutical, biotechnology, cosmetics and medical device laboratories in all of their development projects.

A true ambassador of our expertise, you are working as a consultant in the pharmaceutical industry, with the aim of supporting the management of quality assurance processes in production.

To this end, you are in charge of:

Improve quality: anticipate drifts and malfunctions, implement corrective and preventive actions (CAPA);

Manage deviations: conduct investigations following deviations and ensure communication with the client;

Prepare internal and external audits, supplier audits;

Track change requests and OOS;

Participate in the monitoring of batches, in the process of resolving discrepancies following non-conformities or audits;

Track self-inspections;

Manage milestones/indicators on the Operational Quality side;

Coordinate and monitor Change Controls and approve operational documents related to processes;

Ensure the monitoring of the evolution of the Quality Assurance system of the domain entrusted in accordance with the Quality policy of the site, and the standards in force (BPF, GMP, Public Health Code, ISO standards, etc.);

Advise and propose corrective actions, support the implementation and optimization of quality management systems