This page was automatically translated and may contain errors. View in English.
Morgan McKinley

Quality Assurance Specialist - Deviations

Morgan McKinley

South Dublin, Ireland · करार

अर्ज करणारे पहिले व्हा

अनुभव
५+ वर्षे
पगार
रिक्त जागा
1
पोस्ट केले
७ तासांपूर्वी
कार्य मोड
कार्यालयात
शिक्षण
पदवी
सारांश
अर्ज करणे आवश्यक आहे

तुम्ही जिथे काम कराल

नोकरीचे वर्णन

Role Summary

The Quality Assurance Specialist focusing on deviations offers expertise and supervision for handling deviations, investigations, Corrective and Preventive Actions (CAPAs), and change controls. Collaborating closely with departments such as Manufacturing, Engineering, Validation, Quality Control, and Supply Chain, this position ensures that quality investigations follow Good Manufacturing Practice (GMP) standards, regulatory directives, and organizational policies.

Key Duties

  • Oversee the management and timely execution of deviations, investigations, CAPAs, and change controls with compliance adherence.
  • Evaluate and sanction quality documentation, guaranteeing comprehensive scope, root cause identification, risk evaluation, and effective corrective measures.
  • Act as the Quality Assurance representative in forums including Deviation Review Boards and Change Control Boards.
  • Provide specialist support for complex investigations and advise on compliance and operational quality challenges.
  • Track quality system performance metrics and assist with initiatives aimed at improving processes continuously.
  • Participate in Annual Product Reviews and contribute to quality metric reporting as needed.
  • Support internal quality audits, regulatory inspections, and maintain readiness for inspections.
  • Execute all functions adhering strictly to safety protocols and Standard Operating Procedures (SOPs).
  • Be prepared to broaden responsibilities in line with evolving business requirements.

Qualifications and Experience Required

  • Bachelor's degree in Science, Engineering, Pharmacy, Biotechnology, or closely related fields.
  • At least five years of relevant experience within pharmaceutical or biotechnology sectors.
  • Proven expertise in providing QA oversight for deviations, investigations, CAPAs, and change controls under GMP conditions.
  • Comprehensive knowledge of GMP regulations, quality management systems, and risk control methodologies.
  • Strong analytical abilities paired with problem-solving skills, effective communication, and stakeholder engagement capabilities.
  • Capability to work autonomously while collaborating efficiently across multifunctional teams.
  • Excellent organizational, communication, meeting coordination, and facilitation skills.
  • Evidence of contributing to ongoing improvements in regulated quality environments.

Work styles they’re looking for

संवाद समस्या निराकरण तपशिलाकडे लक्ष संघ सहकार्य संघटनात्मक कौशल्ये

तुम्हाला उत्तर हवे असल्यास तसेच ठेवा — आम्ही त्याचा इतर कोणत्याही गोष्टीसाठी वापर करणार नाही.

ब्राउझ करण्यासाठी क्लिक कराड्रॅग अँड ड्रॉप, किंवा पेस्ट स्क्रीनशॉट

PNG, JPG, GIF, MP4, WebM, MOV · प्रत्येकी कमाल २०MB · ५ फाईल्स पर्यंत

🤖
ऑनलाइन · त्वरित एआय मदत