Medical and safety monitoring of clinical trials to current scientific, ethical, and regulatory standards. Work with the clinical investigators and site staff……
Working cross functionally with clinical, quality and engineering during the design process and throughout the device lifecycle, RA are involved in a broad……
This will require a systems mindset incorporating a cross technology understanding, in addition to a core appreciation of risk and regulatory requirements.…
Lead Auditor qualification desirable but not required. Ensure adequate training is developed and provided to all users on the CAPA/NCEP system and relevant……
The completion and recording of functional and safety checks on plant and manufacturing equipment and correction of any deviations from specification, e.g. air……
Third level qualification in Science, Engineering, a relevant technical discipline or relevant experience. Work as part of the Quality Engineering to provide an……
Co-ordinate and assign daily tasks with Technicians, Inspectors, Operators, etc. Ensuring that process controls are clearly documented and adhered to in……
Lead coordination within artwork production in artwork management system to ensure on time completion. Minimum of 4 - 6 years combined experience from the……
Manage Supplier Change Notifications through to completion. Appropriate qualification in either Purchasing/Productions Planning e.g. Diploma in Purchasing or……
Participate in the OEM/CM material related processes which include: Material Review Board to ensure Coordination of MRB activities with the business unit to……
Reporting to the supervisor (and co-supervisors as applicable), the candidate will work as part of a collaborative research group, but take a hands-on role,……
In addition you will support the overall EHS management system and OHSAS 18001 / ISO 45001 standards which will involve close liaison with EHS engineers.…
Uses current available tools to provide a total solution to the Customer. The ISR will work with the Marketing, AM and/or Regional Manager to formulate hunt……
Assisting in the project definition portion of A3 projects (baseline data gathering). The ability to communicate clearly is imperative, as is the ability to……
Development and implementation of appropriate supporting documentation, and process work instructions compliant with current Good Manufacturing Practices (GMP).…
Working cross functionally with clinical, quality and engineering during the design process and throughout the device lifecycle, RA are involved in a broad……
Comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of……
This will include overseeing scope, schedule and budget including the timely completion of all design and construction activity and the ultimate commissioning……
Demonstrate effective communication skills including: the ability to present information in a clear and concise manner; the ability to facilitate and manage……
Bachelor of Science degree, advanced qualifications such as Masters or PhD is preferred. Work with various in-house functional groups with regards to……
Furthermore, you are taking full ownership of multiple, larger-scale projects, potentially spanning multiple client accounts, in addition to beginning to……
Provide technical support during the NPI process in ensuring that from a Healthcare/Medical device perspective that all FDA, QSR, & MDD standards are achieved……
Furthermore, you are taking full ownership of multiple, larger-scale projects, potentially spanning multiple client accounts, in addition to beginning to……
Collects and documents data acquired during the simulation procedure and accurately inputs this data into ARIA. Responds effectively to patient concerns.…
Acts as the internal liaison between engineering, marketing, manufacturing, RA/QA and sales management for the purpose of scheduling projects, driving the……
Support capacity planning and inventory management strategies to ensure alignment with current and future demand. Provides leadership example to employees.…