Sr Quality Compliance Analyst
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Westport, MO
- Operations
- On-Site
- Full-time
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
AbbVie Ireland is seeking a Senior Quality Compliance Analyst for a 12 month Fixed Term Contract at our Westport site. This role will be central to supporting QA activities relating to one of our combination products, across commercial, clinical, and development operations. The position reports to the Senior QA Manager and interacts closely with the QP and Business Unit Leader to achieve high standards in product quality and regulatory compliance as per EMA, FDA, and relevant regional Ministries of Health.
Responsibilities:
- Collaborate with the Senior Quality Manager to deliver the company's quality plan and ensure compliance with global regulatory requirements.
- Maintain strong working relationships with management, business units, support functions, and both site and global quality functions; confidently communicate quality requirements.
- Provide quality input and guidance on daily activities as a contributing member of the site quality team.
- Coordinate QMS (Quality Management System) management for assigned areas and contribute to overall site quality system overview.
- Bachelor’s degree in a science or engineering discipline.
- Minimum of 5 years’ experience in a quality discipline within the Pharmaceutical or Medical Device environment.
- Demonstrated knowledge of quality standards and regulatory requirements (EMA, FDA, etc.).
- Proven ability to work as part of internal and external teams to deliver projects.
If you are dedicated to ensuring product quality and regulatory compliance and meet these qualifications, we encourage you to apply for this FTC opportunity in Westport.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
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Pay Range: $
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Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.