Vacancies

As a Senior QA Expert, you will hold the ultimate administrative responsibility for preparing and issuing quality-related documentation and certificates applicable to the final product. You will address quality issues and manage quality-related projects within the organization. Additionally, you will conduct internal and external (customer) audits and follow up on and qualify suppliers.

As an experienced Project Manager, you will be engaged in a variety of roles, managing large and small projects in Quality, CMC, Engineering (CQV) or Automation within the Life Sciences Industry in the Netherlands or the DACH region. You will act as a liaison between the client, stakeholders, project team members, suppliers, and installers, often managing personnel from diverse disciplines. Your responsibilities will include planning, quality assurance, and budget control for the projects. You will initiate, plan, execute, monitor, control, and complete these projects independently or with your team of professionals.

As a Project Engineer, you will leverage your strong soft skills and broad technical expertise to oversee projects from design through implementation to testing and validation. Coordination and communication are crucial, as you will collaborate with professionals from various departments to guide projects to successful completion.
Projects typically involve equipment (filling, sterilization, freeze dryers, etc.), pharmaceutical buildings, cleanrooms (building, HVAC, utilities), and more.

As a CSV Specialist, you will be responsible for testing and qualifying process installations and equipment. Additionally, you will organize and oversee testing and qualification/validation activities, acting as the point of contact for relevant departments (such as Production, QA/QC).
Do you have experience with qualification projects? Have you worked within a GMP, GLP, GDP or ISO 13485 environment? If so, please read on!

As a hands-on CQV Engineer, you will be an integral part of a project team, overseeing the commissioning, qualification, and validation of GMP facilities, process equipment, and critical building and utility systems within our client’s life sciences production facility. This role encompasses the design, implementation, and documentation of these qualifications, along with their life-cycle management, ensuring compliance with all applicable regulatory and internal quality standards (FDA and/or EU regulations).