Systems GxP, data integrity, quality, validation

Computer systems validation consultant, LYON

Reference : JL 10/001

We are a fast growing engineering / consulting company, carrying out flat-rate validation projects for computerized systems in the pharmaceutical industry.

To support our strong development, we are looking for two high-potential collaborators who can take charge of the validation of computerized systems.

As part of several large-scale projects that our clients have entrusted to us (new installations, equipment, information systems, etc.), you intervene to pilot validation projects for computerized systems (ERP, LIMS, MES, GED, etc.): finalization. user needs, follow-up of supplier consultation files, development of the validation strategy, design qualification, interface with user and project services, risk analysis, review and coordination of supplier tests, management of qualifications, writing of SOP. You are the guarantor of our know-how, respect for quality, cost and deadlines (lump sum projects).

With a higher education (Engineer, experienced technician, etc.), you have first experience in conducting validation projects or implementing computerized systems in a pharmaceutical context (GAMP, cGMP’s, BPF, GLP, Part11 standards, etc.).

Your organizational skills, your respect for quality requirements, your commitment capacity, your autonomy, your conviviality and your quality of communication will allow you to succeed in this position.

Your leadership and management potential will allow you to evolve very quickly towards positions of responsibility within a structure with little hierarchy, on a human scale, in full development and with recognized expertise.

We offer you a permanent contract, motivating projects, very attractive remuneration, responsibilities and immediate development opportunities.

This position is based in LYON.

If you are interested in this position, send your application under the reference JL 10/001 at : PHARMASYS


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