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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Quality Assurance Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLimerick, IrelandNo salary listed

About the Job

Requirements

  • The Associate Specialist level requires a BS/BA in a scientific discipline or related field, or an equivalent combination of education and experience.
  • The Specialist level requires a BS/BA in a scientific discipline or related field and at least 3 years of relevant work experience in the pharmaceutical or a related industry, or an equivalent combination of education and experience.
  • The Senior Specialist level requires a BS/BA in a scientific discipline or related field and at least 5 years of relevant work experience in the pharmaceutical or a related industry, or an equivalent combination of education and experience; alternatively, it requires an MS and at least 4 years of relevant work experience.
  • The role requires organisational skills and attention to detail.
  • The role requires the ability to learn and use computerised systems for daily tasks.
  • The role requires strong written, verbal, and interpersonal communication skills to interact cross-functionally.
  • The role requires the ability to prioritise, manage multiple tasks, and meet deadlines.

Responsibilities

  • Provide QA oversight and support for manufacturing operations, serving as the primary quality representative within production areas.
  • Partner with cross-functional teams to facilitate issue resolution, including troubleshooting equipment, process, and schedule disruptions, while ensuring appropriate documentation and quality oversight.
  • Assess and triage potential non-conformances in real time, ensuring required information and documentation are secured to support investigations.
  • Review and approve documentation associated with routine and non-routine manufacturing activities, including area clearances, incursions, changeovers, and other operational events.
  • Participate in shift meetings and operational discussions, providing quality mentorship, observations, and recommendations related to ongoing activities and containment actions.
  • Provide quality consultation and guidance in alignment with QA policies, procedures, and regulatory expectations.
  • Represent Quality Assurance in managing complex deviations, change controls, CAPAs, and other quality systems, including actively participating in investigations, root cause analysis, and corrective action implementation.
  • Support employee development through training, coaching, and mentoring on QA processes, procedures, and standards.
  • Perform activities related to product disposition and release, including reviewing manufacturing records and supporting documentation.
  • Review and approve investigations associated with product, process, and manufacturing events.
  • Identify opportunities for continuous improvement and support initiatives that improve product quality, compliance, and operational efficiency.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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