Site Quality & Compliance Specialist

Regeneron Ireland

Limerick

On-site

EUR 52,000 - 70,000

Full time

7 days ago
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Benefits offered by this job

Annual bonuses
Equity awards
Pension benefits
401k match
Health & wellness programs
Fitness centers
Insurance benefits
Paid time off
Family support

Job summary

Regeneron Ireland seeks a Temporary Quality Compliance Specialist to join the Quality Assurance Raw Materials team at the Raheen site in Limerick. You will ensure compliance across all quality aspects, oversee quality systems, and participate in audits and improvement initiatives.

The role requires a BSc/BEng in a scientific field and 3+ years of relevant pharmaceutical experience. Competitive benefits and a dynamic, fast-paced environment are offered.

Qualifications

  • Requires a quality mindset with meticulous attention to detail and adherence to quality systems.
  • Experience working in pharmaceutical or related industry is preferred.
  • Demonstrates strong communication and collaboration across functions.

Responsibilities

  • Ensure compliance with all aspects of Quality for the Raheen site and oversee site quality systems.
  • Review and approve failure investigations, change controls, CAPA and deviations.
  • Maintain electronic systems used for Change Control and Deviation Management.
  • Review procedures and policies to ensure compliance with regulatory requirements.
  • Monitor and trend metrics related to site quality systems.
  • Participate in regulatory and customer audits and quality risk assessments.
  • Collaborate with departments to resolve issues and maintain compliance.

Skills

Quality mindset
Attention to detail
Interpersonal skills

Education

BSc/BEng in scientific discipline or related field

Job description

Regeneron Ireland seeks a Temporary Quality Compliance Specialist to join the Quality Assurance Raw Materials team at the Raheen site in Limerick. You will ensure compliance across all quality aspects, oversee quality systems, and participate in audits and improvement initiatives.

The role requires a BSc/BEng in a scientific field and 3+ years of relevant pharmaceutical experience. Competitive benefits and a dynamic, fast-paced environment are offered.

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