Executes manufacturing operations to perform operations including but not limited to equipment cleaning and set up as well as stream specific operations like:Upstream: Vial Thaw, Inoculation, Cell Culture and RecoveryDownstream: Chromatography, Filtration, Ultrafiltration, Final FillingCentral Service: Buffer/ Media Preparation, Autoclave, Glasswash and cleaning processes, Sampling of raw materials.
Carry out daily tasks as assigned by Lead Biotechnologist or Manufacturing Supervisor
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Act as secondary contact for Pharmacovigilance activities, monitoring post‑marketing surveillance, adverse events, product complaints, recalls, and field safety corrective actions, while supporting investigations, deviations and CAPAs.
Collaborate closely with HQ, local teams and external partners, maintaining regulatory documentation and databases, supporting tender documentation, and contributing to the standardization and continuous improvement of regulatory and quality practices across the region.
Supports multi-discipline manufacturing processes with respect to the repair, maintenance, installation and/or enhancement of a select group of machinery and equipment or interrelated systems.
Provides technical support in the area of chemical, electronic or mechanical operations, tests, experiments and/or problem resolution associated with components, parts, products or processes/systems.
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Lead the planning and execution of advanced NDE jobs. Provide expert interpretation of inspection results. Provide integrated analysis support with fracture mechanics experts.
Support failure investigations and root cause analysis by providing NDE expertise.
Developing detailed technical requirements of the purchase specification. Act as Engineering interface and review Request for Quotation (RFQ) as needed by sites or projects.
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Partner with cross-functional teams to identify product risks, investigate potential failure modes, and implement effective risk control measures.
Ensure compliance with ISO 13485, FDA regulations, customer requirements, and applicable quality standards.
Develop, review, and maintain quality procedures, SOPs, and documentation to support product development and Quality Management System (QMS) requirements.
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Language requirement: Written and spoken fluency in English
Internship period : January to June 2027
Application deadline: As applications will be reviewed on a rolling basis, we recommend applying as soon as possible for your application to be considered. This vacancy will be closed once we have enough applications for consideration.
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Ensure adherence to established data governance policies and business rules, advocating for their importance among team members and business users
Guide and support business users through changes in data management processes, data policies, and/or business rules to ensure smooth transitions and minimal disruption
Request, approve and/or oversee data maintenance requests, ensuring they align with data policies and business rules
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