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QC Analyst

ID
15419
Location
Cork, Cork
Role Type
Contract

QC Analyst

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Quality Control (QC) Analyst – Microbiology

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 years’ experience as a Microbiology QC Analyst within a pharmaceutical environment.
  • Ideally 5+ years’ 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.
  • Demonstrates integrity and Credo-based actions at all times.

Our Vision: To be recognised as the best STEM Contracting & Permanent Recruitment company and the Employer of Choice for top performing Recruiters.

For further information on this role please contact Geraldine Gormally on 0861071395  / recruit@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/  

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel

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