The Associate Director, Quality Assurance will report to the Senior Director, Quality Assurance Drug Product and oversee the quality assurance for combination product projects from inception to commercialization. The ideal candidate will have a strong background in drug delivery systems, medical devices and combination product regulations. This role will involve collaboration with cross-functional teams and external partners to ensure that the combination product meets regulatory standards.
This position performs supervisory work in the inspection of buildings, other structures, and/or devices in the assigned discipline/s for conformity with NYC Construction Codes, Department rules, other pertinent laws and rules, and approved plans and specifications. The Supervising Inspector assists and supports the Chief and Assistant Chief with daily operations. Monitors, adjusts and approves inspectors’ routes and submitted inspection record per relevant protocols.
Interested in speaking to Auditors who would be interested in supporting RQM on various internal audits on a contract basis for our clients in the U.S. Responsible for project management, audit planning, executing the audit within the allotted time, issuing the audit report within the allotted time and the approval of the final audit report. Providing the clients with 80% auditor (hats on) and 20% mentor (hats off).
This is a unique opportunity to travel, mentor, and directly impact how our installation teams deliver craftsmanship, accuracy, and customer satisfaction across new and existing markets. You will train and coach Field Technicians on accurate window measurement, installation, service, and audit best practices and conduct on-site evaluations and feedback sessions to ensure safety, accuracy, and customer satisfaction.
As a Quality Control Inspector, you'll report to an Inspection Team Leader and work as part of the Operations team. Your role involves checking email daily, attending inspections on time, performing merchandise inspections, supervising container stuffing, and fulfilling inspection reports according to company procedures.
This role involves executing quality processes independently, including quality control, maintenance, and record-keeping, ensuring compliance and high-quality output. It requires assessing performance, developing tools, and improving processes to meet customer demands and organizational goals in a temporary, yet impactful role.
The Manager Manufacturing will be responsible for managing the manufacturing and import of medicinal products and investigational medicinal products in compliance with §12 AMWHV, GMP, and regulatory requirements. This role ensures timely batch review, product testing, documentation, and release to the Qualified Person, while helping to maintain GMP-compliant facilities, partners/suppliers and optimized processes. This person collaborates and actively works within Quality Assurance to manage deviations, CAPA, audits, and regulatory compliance.
As a Quality Inspector, you’ll report to the Inspector Team Leader or Operations Manager. You will be performing on-site quality inspections of our clients’ products and ensuring that all the work is performed to the QIMA standard of quality.
As a Performance Engineer, you will be responsible for creating and implementing performance testing. You will work on complex distributed systems, databases, and large clustered datasets, focusing on optimizing overall product performance. Collaborate with various teams to review requirements, execute tests, and troubleshoot issues to deliver high-quality initiatives.
Start in January 2026 as an Intern Quality & Food Safety at our office in Utrecht. In this internship, you will help us optimize the quality and food safety processes within the Operating, Routesales & Quality department of our Professional branch. Your most important tasks will be carrying out an independent project related to structural quality improvement, process optimization and/or food safety.