Senior Quality Assurance Advisor Jobs in British Columbia

Extensive knowledge of Quality System regulatory requirements, including 21 CFR 820, 21 CFR 210 and 211

Minimum 10 years’ experience combined in quality unit and manufacturing in the biotech regulated industry or equivalent

GMP experience in biotechnology, pharmaceutical, or life science field is required

Experience building teams and managing people leaders

Establish and maintain Quality systems required for new product introduction, technology transfer, manufacture and distribution of new and regulated STEMCELL products

Leads QA evaluations, and creation and execution of quality strategic planning to ensure compliance and business needs

Experience in MS Office, Excel, and database management

Business / Project management skills (e.g. schedule, cost, resource planning, etc.)

Collaborate with multidisciplinary engineering and project management teams to mitigate the risk associated with quality system implementation and safety in design

Familiarity, understanding, knowledge, and previous experience of the following:

Free access to our Aspire Academy for continuing professional education

Medical and dental benefits once qualified

Excellent project management skills, advanced written and verbal communication skills

Direct fieldwork daily, inform supervisors of the engagement status, and manage staff performance.

Use technology to continually learn, share knowledge with team members, and enhance service delivery.

Learning opportunities to develop new skills and progress your career

Develop and maintain productive working relationships with client personnel and assess clients' satisfaction.

Proactively maintain contact with the client throughout the year.