Requirements: English, French
Company: PQE Group
Region: Nord-Pas-de-Calais , Hauts-de-France
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia, and the Americas. Due to our constant growth, we are looking for a full-time Process Engineer with expertise in Commissioning, Qualification, and Validation (C&Q) to join our team. The ideal candidate will have over 3 years of experience in C&Q, SAT (Site Acceptance Testing) for assembly and packaging processes in the Pharmaceutical or Medical Device industry. SAT Testing: Plan, execute, and document Site Acceptance Testing (SAT) for assembling and packaging equipment, ensuring compliance with regulatory and quality standards C&Q Activities: Lead Commissioning, Qualification, and Validation (C&Q) activities, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) for new or modified equipment Stakeholder Collaboration: Work closely with internal stakeholders, vendors, and contractors to ensure successful project execution and alignment with business goals Training: Provide training and support to operations and maintenance teams on new equipment and processes Bachelors degree in Engineering (Mechanical, Chemical, or related field) Experience: 3+ years of experience in the Pharmaceutical or Medical Device industries in C&Q , SAT testing , and process engineering, preferably in assembly and packaging operations Language: Fluency in French (written and spoken) is required. Proficiency in English is a plus PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.