Senior Quality Assurance Professional
1 week ago
We are seeking a highly skilled and experienced Senior Quality Assurance Professional to join our team at Joulé. This is an excellent opportunity for a motivated individual to contribute to the success of our organization.
About the Role:The Senior Quality Assurance Professional will be responsible for ensuring the successful implementation of new quality management systems (QMS) by assisting with project-specific tasks, including project support, document management, documentation review, technical editing, meeting coordination and facilitation, training, onboarding, and other administrative tasks.
- Perform documentation review and technical editing to ensure consistency within the Redesign Team and across the Clinical Supply network.
- Serve as a communication channel between global network site personnel.
- Assist with site metrics collection/reporting and sharing of success stories/achievements.
- Support development of the learning strategy for new and revised QMS topics, including access to LMS content and generation of reports, creation of training materials and communication of training requirements.
- Support project management activities, optimization of communication strategy and change management strategy.
- Management of document lifecycle (new or existing documents) and review/approval workflows.
- Maintain electronic repository/communication mechanism (e.g. QMS SharePoint Site, Microsoft Teams).
- Serve as a change agent helping the Clinical Supply QMS Redesign Team drive culture change.
To be successful in this role, you will need:
- Bachelor's Degree in an appropriate scientific or business field of study.
- Minimum of five (5) years' experience in the Pharmaceutical or equivalent industry.
- Strong technical knowledge, skills, and experience in project and documentation management.
A strong candidate for this role will have:
- Excellent verbal and written communication skills as well as presentation skills.
- Strongly developed cross-functional teamwork and collaboration skills.
- Experience in Microsoft tools such as Outlook, Word, Excel, PowerPoint, SharePoint, Teams and Project.
- Experience directly related to the development of Quality Standards and core requirements for Market Supply and/or Clinical Supply.
- Experience directly related to Quality Assurance, Quality Control, GMP regulations or pharmaceutical regulations.
- Knowledge of process mapping and optimization.
The estimated salary for this role is $80,000 - $110,000 per year, depending on experience. We also offer a comprehensive benefits package, including health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
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