We are specifically looking for a trainee who, after completing a training program, will start working for one of our clients. You will work on projects in the pharmaceutical industry at the intersection of science and ICT.

As CSV consultant you execute computer validation projects on location at the customer or from our offices. You are involved with the analysis of user requirements, testing and implementation of new software solutions. Our customers in the pharmaceutical industry count on your expertise related to regulatory requirements and your insights to manage project risks.

We are always looking for freelance consultants to strengthen our team. We are seeking a wide range of expertise: QA, Validation, CSV, ICT, Engineering, GMP Production Support, Project and Interim Management.

As a QC Analytical Method Validation Consultant you support and execute routine and project related analytical method validation activities. You support the development, improvement and/or transfer of QC methods, including the writing and review of related documentation. You support the organization during internal and external audits.

As a quality assurance consultant you work with customers in the pharmaceutical industry to ensure quality on projects or during routine operations. You review quality critical documents and records, and you ensure the quality management system of the client is correctly followed. Depending on your background and your level of experience you also give advise on regulatory requirements, facilitate risk assessments and investigations, you assist during regulatory inspections, give training and might even be asked to conduct internal or supplier audits on behalf of our customers.

We are looking for a trainee who will work with one of our clients in the pharmaceutical industry after completing a training program. No work experience is required for this job, as we provide an appropriate training program.

As validation consultant you execute validation projects on location at clients in the pharmaceutical industry. This can be production equipment validation, lab equipment validation but it can also concern the validation of facilities and utilities, processes and computer systems. Depending on your background and interests you will be active in one or more of these areas.

Our customers count on your expertise related to regulatory requirements and your insights to manage project risks. You are responsible to write documents such as validation plans, FMEA risk assessments, URS, IQ, OQ and PQ. Also you execute or follow-up on the execution of validation test runs.