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The associate supports the supplier qualification process by conducting quality risk assessments and maintaining the Qualified Supplier List. They also coordinate with internal SMEs and the wider QA team to ensure compliance and audit readiness for clinical suppliers.
Job Overview:
The Associate plays a key role in our Supplier Qualification Office (SQO) within Global Regulatory Compliance & Quality Assurance in supporting the qualification of third-party clinical suppliers. As a member of the SQO team, this position will be responsible for supporting the quality risk assessment of third-party suppliers, who provide services/ products that directly support clinical trials.
Summary of Responsibilities:
CAPA/ audit support
Participates in and supports other initiatives as required
Experience (minimum required):
Experience working independently with minimal supervision and in a team environment under time and resource pressures
Excellent interpersonal, oral and written communication skills when dealing with both external and internal customers with an ability to prioritize and meet deadlines
Good presentation skills
Proficient with MS Office programs
Proactive self-starter
Multi-tasker
Creative problem solver (to improve processes, create new approaches)
Excellent Project Management skills to ensure proper proactive planning and follow up
Well Organized
Team player
Enthusiastic agent of change
Qualifications (minimum required):
Work environment:
Physical requirement:
Learn more about our EEO & Accommodations request here.
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