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Quality Assurance Manager

📍 Groton, CT 🕒
Work Model
📍 Groton, CT
Employment
💼 Full-Time Direct
Recruitment Type
🛡️ Direct to HR Pipeline
🛡️
Human-Verified Opening: Inspected by Sarah Jenkins, CIPD • RemoteVault Editorial Team. Authenticated directly from Integrated Resources, Inc ( IRI )'s hiring pipeline • Zero recruiter markups or candidate fees. Verification Standards →

📋 Role Overview & Responsibilities

Title: Quality Assurance Manager

Location: Groton, CT (Hybrid: Required Onsite 2-3 days per weeks) Support US and UK time zones

Duration: 18+ months

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 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 various roles or assignments to 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.

Hard Skills: 1. Vendor Quality Management Exp. in Pharma industry 2. CGMP, not GCP 3. Project management 4. MS Office Plus Skill: 1. Relationship building 2. Negotiation 3. Auditing 4. SAP

BS Preferred (open to 5 + years' experience in lieu of degree)

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This position is located in Groton, CT with potential relocation and sponsorship assistance depending on candidate qualifications.

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