BIOVECTRA Inc. has an opening for a Process Validation Associate. This is a full-time permanent position located in Windsor, NS.

The candidate will be responsible for:

• Assisting in the establishment of the tech transfer, scale up, and validation strategy for new processes/equipment and translates those requirements to appropriate validation protocols and standard operating procedures.
• Working with the Process Development Group to ensure appropriate critical process parameters are implemented, justified, and measured to control the process critical quality attributes.
• Identifying potential scale up obstacles and working with Engineers, Quality Assurance, Process Development and Manufacturing professionals to ensure validation risks are mitigated and controlled.
• Leading participant in conducting process risks analysis and process hazard analysis.
• Developing, maintaining, and updating the Validation Master Plan (VPM) for the overall project.
• Qualification of new equipment/processes, computer-related system qualification and calibration program management.
• Reviewing detailed plant layouts, procedures, and equipment specifications (URS) to ensure the project progress and quality / regulatory compliance.
• Conducting and/or participating in deviation investigations to identify root causes and define corrective and/or preventative actions (CA/PA), maintaining compliance within the company.
• Communicating and reporting the status of each project to the management and department that sponsors the project.
• Working as part of a multi-disciplinary team.
• Reviewing and updating Standard Operating Procedures to ensure appropriate content.
• Providing technical expertise and oversight on various technical documents (BPR's, New Product Validation Reports, etc.).
• Assisting in multiple complex technology transfer projects related to the manufacturing and testing.
• Authoring and reviewing technical documents including standard operating procedures, testing protocols, technical reports, batch files and technical transfer documents.
• Adhering to BioVectra's Health and Safety Policy as outlined in CP0010 Occupational Health and Safety Policy, Statements of Principle, and Responsibilities.
• Additional duties assigned, based on business needs and the department supervisor's request.

The successful candidate for this position should have:

• Bachelor of Science in Chemistry, Biochemistry, Bioengineering, Biology, Chemical Engineering, or related field.
• Three years GMP pharmaceutical processing experience.
• Statistical analysis tools and methods.

BIOVECTRA offers a competitive salary and benefit package. Interested candidates are asked to apply by choosing the "Apply Now" button below.

Closing Date: May 10, 2024