Biodextris
Project Coordinator
The Project Coordinator uses scientific and professional knowledge/experience in accordance with regulatory requirements to lead projects from start to completion. The Project Coordinator manages the required activities to meet client’s requirements in term of timelines, deliverables, and budget. The Project Coordinator interacts with other departments’ heads to ensure that the required resources are available for completion of the project. She/He may coordinate portions of projects managed by other project managers. She/He provides project updates to peers and clients in a timely and efficient manner.
Documentation Specialist
The Documentation Specialist is part of the QA department and is the central contact person for the management of documents related to Quality Systems. The Documentation Specialist ensures the proper operation, tracking and maintenance of these systems and serves as the main administrator of the Official Documentation list and filing systems to ensure their accuracy and continued compliance.
Analytical Scientist I
The Analytical Scientist I uses professional knowledge and company's policies and procedures to execute tasks and solve a variety of problems within the Analytical department. The Scientist I executes analytical procedures and ensures compliance with predefined assay acceptance criteria and product specification.
Bioprocess Technician
The Bioprocess Technician is part of our Bioprocessing team and provides support functions to enable process design and optimization for development, preclinical and early clinical phase programs.
Quality Assurance Associate
The Quality Assurance Associate is responsible for supporting the implementation, execution and maintenance of quality systems and programs. The QA Associate will ensure continuous compliance with Canadian, US and European quality compliance regulations and requirements.
Downstream Process Scientist
The Scientist will be responsible for the independent design, planning and execution of complete upstream processes for R&D, non-GMP or GMP projects, depending on specific project scope and client requirements.
Logistics Associate
We are currently seeking a qualified candidate for the Logistics Associate position, responsible for all shipping/receiving activities at our new CDMO facility.
Commission, Qualification and Validation (CQV) Associate
Candidates must be capable of developing a technical understanding of bioprocessing and laboratory equipment, and comfortable with working within a highly regulated environment. Experience in validation, operation or maintenance of relevant equipment, facilities or utilities is preferred.
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