The Company A leading global biotechnology organization, dedicated to developing and delivering innovative medicines to improve patient outcomes. Operating worldwide, the company combines science, technology, and quality-driven processes to ensure safe and effective clinical products.   Role Description As a QA Associate , you provide onsite Quality Assurance support within the production area. You act as a key point of contact for quality related matters, ensure compliance with GMP standards, and review batch documentation for products assembled, packaged, and labeled, ready to be distributed. Responsibilities – Provide daily QA guidance in production areas to ensure compliance with SOPs and work instructions – Act as first point of contact for quality related questions during packaging and labeling – Review and approve batch production record entries prior to manufacturing activities – Perform in-process and finished product checks  –  Compile, review, and prepare batch records for QP disposition – Conduct GMP compliance checks and support deviation handling – Author or review SOPs and work instructions – Support GMP training activities for QA and production teams Requirements – MBO or BSc in Life Sciences,…

Company A leading global biotechnology organization dedicated to discovering, developing, and delivering innovative medicines for patients with serious illnesses. Driven by science and powered by advanced technology, the organization focuses on areas such as oncology, cardiovascular disease, inflammation, and rare diseases. Its mission is centered on improving lives by turning cutting-edge science into meaningful therapies that address unmet medical needs.   Job Description We are seeking a detailed-oriented Quality Assurance Associate to join the team. This role is responsible for reviewing and approving critical master data and artwork related to medicinal products, maintaining QA systems, and supporting compliance with GMP standards. The ideal candidate will work closely with various departments to ensure quality integrity and support continuous improvement initiatives.   Responsibilities Review and approve SAP master data and artwork for medicinal products to ensure accuracy and compliance. Maintain and improve QA systems, monitoring their performance regularly. Collaborate with the Global Artwork Center, Master Data, SCPM, site SMEs, Regulatory Affairs, and QA management to ensure seamless processes. Author, review, and approve operational SOPs and Work Instructions related to quality assurance procedures.…

Company A leading biotechnology company dedicated to serving patients worldwide. The organization operates a global supply chain network, manufacturing and distributing medicines and clinical research products. With a diverse team of professionals from multiple countries, it focuses on innovative healthcare solutions and improving patient outcomes.   Job Description We are seeking a detail-oriented and experienced Clinical Supply Chain Associate to join the team. In this role, you will oversee the efficient and compliant distribution of investigational products to clinical sites around the world, ensuring timely delivery and adherence to regulatory standards.   Responsibilities Manage the sales order and stock transfer order processes efficiently. Review temperature data and manage temperature excursions, ensuring compliance with regulatory standards. Control and monitor the site and transit temperature excursions, as well as handle returns and reconciliations. Support expiry relabeling campaigns and manage import licenses. Process and handle distribution complaints promptly. Ensure timely and compliant shipping of investigational products to clinical sites and logistics service providers. Collaborate closely with Clinical Customer Service, Development Supply Chain stakeholders, QA, warehouse teams, clinical site monitors, and couriers to resolve…

Company A leading global biotechnology organization dedicated to discovering, developing, and delivering innovative medicines for patients with serious illnesses. Driven by science and powered by advanced technology, the organization focuses on areas such as oncology, cardiovascular disease, inflammation, and rare diseases. Its mission is centered on improving lives by turning cutting-edge science into meaningful therapies that address unmet medical needs.   Job Description As a Manufacturing Process Technician you will be support the operation of semi-automated production lines within a GMP-compliant environment, ensuring efficient and accurate delivery of production targets across various shifts.   Responsibilities Operate on packaging or assembly lines in accordance with standard operating procedures, ensuring product quality and safety (folding boxes, applying labels, etc.) Collaborate closely with colleagues and line leads to meet daily production goals Escalate issues or deviations clearly and promptly to the line lead. Take ownership of assigned tasks, follow procedures diligently, and escalate when necessary Participate actively in shift handovers, ensuring seamless communication between teams Complete all required training and certifications on time Adhere to safety, quality, and productivity standards during all shifts  …