Senior Quality Assurance Specialist
3 weeks ago
- Perform adherence checks as applicable
- Facilitate and/or Lead product complaint/inquiry requests, investigations and trending as per client or Kuehne+Nagel requirements
- Monitor temperature conditions of the facilities if applicable review inbound product temperature conditions;
- Maintain site documentation control and records retention for all local forms, WIs, SOP's, and client specific documentation
- Review, sign off, and oversee QA records such as certificates of destruction, calibration records, sanitation, etc.
- Facilitate deployment and development of training strategies
- Train and oversee Level I and II staff as assigned
- Support Operations in the maintenance of the site training program and applicable documentation;
- Oversee and/or execute development and implementation of change controls, WI’s, and SOP’s using working knowledge of GMP’s and industry standards
- Support the development of pro-active strategies as preventive measures against potential future issues within the QMS
- Assist QA Manager with new client / product onboarding / setup preparation
- Oversee day to day activities of QA Specialists, monitoring of work quality and productivity as assigned by the QA Manager
If you require an accommodation for the recruitment /interview process (including alternate formats of materials, or accessible meeting rooms or other accommodation), please let us know and we will work with you to meet your needs.
Your Skills and Experiences- Bachelor in Sciences (e.g. Pharmacy, Chemistry, Biology or a related discipline) is required
- 5+ years industry experience in Medical Device/Pharmaceutical industry in QA
- 3+ years industry experience in Medical Device/Pharmaceutical distribution site is preferred
- Meet Health Canada's requirements to perform RPIC and QPIC responsibilities
- Strong knowledge of Quality Management systems and standards (i.e: GMP, ISO 13485, ISO 9001)
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