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Job Description
- Req#: 25-52687
Supports the separation effort across businesses, with a focus on product rebranding, to ensure adherence to timelines.
Supports quality planning documentation and task closure, while ensuring compliance to process.
Assist strategies for efficiencies to minimize duplicative efforts
Support performance and/or documentation for testing protocols and reports
Perform review and update of quality-owned docunents for updates
Supports efforts of Rebranding Program Leaders to prioritize projects and tasks.
Communicates and tracks task progress and closure, escalates issues related to quality or timeline attainment using tools
Position Qualifications
Technical education in quality or related field.
5+ years of work experience in Medical Device and/or Drug Quality.
Cross Functional team experience.
Preferred
Proficiency with Microsoft Office applications including but not limited to Word, Excel, Access, PowerPoint, Project, Outlook, Power BI.
Effective team and peer collaboration skills
Ability to effectively navigate multiple systems related to inventory or document management such as SAP or ENOVIA/PLM
Demonstrated good documentation and communication skills.
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.About the company
Mindlance is one of the largest diversity-owned staffing firms in the US . As a recruitment centric talent acquisition company, Mindlance provides Technology, Engineering, Digital / Creative / Marketing, Clinical Research, Scientific, Finance, Professional and Payroll Management staffing services to Global 1000 companies across the US, Canada and India.
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