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QC Analyst

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  • IE
    Ireland
  • IE
    Ireland

About

Senior Quality Control (QC) Analyst โ€“ Microbiology


Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.

Location: Onsite 5 Days per Week


Department: Quality Control


Role Overview

  • The purpose of this role is to define the duties, responsibilities, and authority of the Quality Control Analyst within the Quality Control Department at JPS.
  • The QC Analyst is responsible for carrying out microbiological quality control testing and associated laboratory activities in compliance with GMP requirements. The role involves collaboration with cross-functional departments to ensure efficient and compliant QC operations.
  • This position operates within the Quality Control Department at JPS and applies specifically to the role of Quality Control Analyst (Microbiology).

Key Responsibilities

  • Execute tasks and projects related to equipment, laboratory utilities, and testing procedures in accordance with GMP.
  • Partner with cross-functional teams to ensure QC testing activities are completed efficiently.
  • Participate actively in QC team initiatives, including:
  • QC Material Release & Scheduling Activities
  • QC Key Performance Indicators (KPIs)
  • QC Training (Personal competency and team development)
  • QC Documentation Review & Approval
  • Site Cross-Functional Teams
  • Deliver against departmental goals, objectives, and continuous improvement initiatives.
  • Support internal and external audits as required.
  • Maintain and develop knowledge of analytical methods, technologies, and regulatory compliance requirements.
  • Comply fully with EHS rules and procedures.
  • Foster a culture of quality, safety, and compliance aligned with the J&J Credo.
  • Review and update the Job Description in collaboration with the Team Leader as required.

Minimum Requirements

  • Minimum 3 yearsโ€™ experience as a Microbiology QC Analyst within a pharmaceutical environment.
  • Ideally 5+ yearsโ€™ experience in pharmaceutical quality or compliance roles.
  • Broader industry experience is highly desirable.
  • Strong understanding of GMP requirements and regulatory expectations.

Education

  • Third-level Degree in a Science or Pharmaceutical discipline.

Key Skills & Competencies

  • Builds strong, productive working relationships.
  • Demonstrates ability to work effectively both independently and within teams.
  • Holds self-accountable for compliant and flawless execution.
  • Strong written and verbal communication skills.
  • Innovative and solution-oriented mindset. xcfaprz
  • Demonstrates integrity and Credo-based actions at all times.

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  • Ireland

Languages

  • English
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