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Quality Assurance Manager
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Quality Assurance Manager
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The Fountain Group Groton, United StatesThe Fountain Group is currently seeking a · Supplier/Vendor Quality Assurance Manager · for a prominent client of ours. This position is located in · Groton, CT (Hybrid role) · . · Details for the position are as follows: · Payrate: $50/hr W2 · Job Title: Supplier/Vendor Q ...
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Quality Assurance Manager
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Quality Assurance Manager
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Quality Assurance Manager
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Quality Assurance Manager - Groton, United States - Integrated Resources
Description
Job Title: Quality Assurance Manager
Job Location: Groton, CT (Hybrid)
Job Duration: 18 Months +
Pay range: $48.87/Hr. on W2
Job Description:
· You will be a proactive partner with the external supply business lines, clinical product development teams, maximizing the contribution of Global Quality Operations with our external contract vendors.
· You will be the Vendor Point of Contact responsible for the quality management of approximately 25 contract manufacturers, packager, contract test laboratories, and supply partners globally.
· As a Quality Manager, you will focus on developing relationships, independently negotiating, developing, and communicating Client's quality requirements with contract vendors.
· Your expertise provides quality system leadership to operational teams, drive process improvement, advancing new concepts and methodologies that will make client ready to achieve new milestones and help patients worldwide.
· Provide guidance, lead/co-lead projects, manage own time to meet objectives, plan resource requirements for projects across the Department.
· Contribute to Quality Assurance by undertaking a variety of roles or assignments to further develop internal processes and people.
· Assess the operations executed at the supplier for their adherence to regulatory requirements, Quality Agreement requirements and client expectations.
· Conduct quality reviews and report on results or defined quality analytics to in-country Medical Management, Platform Lines and Regional Medical Quality group, as appropriate.
· Provides project support with current Good Manufacturing Practices to clinical supply packaging operations.
· Provides guidance on procedures and training necessary to be in complete compliance with current GMPs.
· BS Preferred (open to 5 + years experience in lieu of degree)
Schedule: Required Onsite 2-3 days per weeks. Support US and UK time zones.