Quality Assurance Intern

Quality Assurance Intern JR000014824 Quality Assurance Intern (Open) Dublin, IRL The Company
Mallinckrodt is a company united around a central pursuit – improving outcomes for underserved patients with severe and critical conditions. As a purpose-driven organization with a broad network and relentless determination, we create products, delivery systems and solutions for patients whose needs have not been met.

Mallinckrodt is a global business consisting of multiple wholly owned subsidiaries that develop, manufacture, market and distribute specialty and generic pharmaceutical products and therapies. With locations in the US, Canada, Europe and Asia, culture is one of the most important aspects of our organization. Who we are at the core of our company - how we think, feel and work together means everything. We are anchored in our values of Patient Centricity, Innovation, Collaboration, and Integrity.

The Company's Specialty Brands reportable segment's areas of focus include autoimmune and rare diseases in specialty areas like neurology, rheumatology, hepatology, nephrology, pulmonology, ophthalmology, and oncology; immunotherapy and neonatal respiratory critical care therapies; analgesics; cultured skin substitutes and gastrointestinal products. Its Specialty Generics reportable segment includes specialty generic drugs and active pharmaceutical ingredients. We are focused on listening to needs and delivering solutions. We provide medicines to address unmet patient needs, stemming from 155 years of using our unique strengths, experience, and expertise to help improve people's lives.
We know that we contribute to something that matters because we make quality products that impact patient lives. We have built an inclusive community and recognize the importance of every employee as a whole person – inside and outside of work. Our dynamic work environment provides unique experiences for employees to grow and develop.

We are moving forward – come with us.

• Help perform and evaluate trending of the Quality Management Systems to support management reviews, investigations, and continuous improvement initiatives (i.e. quality management reviews, annual product quality reviews, trend analysis for quality events, etc.)
• Interpret and properly apply all applicable regulatory requirements
• Support investigations through cross functional team involvement (i.e. RCA, etc.)
• Improve existing procedures or create new procedures to align with cGMP and regulatory requirements
• Review procedures, protocols, reports, etc., as required
• Assist with continuous improvement, compliance-based, and site projects
• Support lean manufacturing initiatives both at the site level and within the greater Quality/Operations organization
• Participate in internal audits as a SME or member of the audit team
• Perform additional duties as directed by management
• Support the day to day management for QA Team and associated workload.

• Support other Quality functions at the site through cross-training opportunities
• Help drive Continuous Improvement projects on site from a Quality Perspective
• Ensure Compliance with current regulatory requirements

• Bachelor’s degree or higher in a scientific discipline (biology, chemistry or engineering)
• Effective communication and presenting skills
• Ability to manage change
• Self-motivated
• Independent and sound decision making capabilities
• Team-oriented
• Deliver on-time results / Time Management

• Proficient with the Microsoft Office Suite, especially Excel, Word, and PowerPoint