Analyst Quality Control

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for the best talent for a an Analyst Quality Control to be in Cork.

This position is responsible for carrying out tasks and projects related to equipment lab utilities and testing procedures at Janssen Sciences Ireland (JSI) as required by Good Manufacturing Practice (GMP). Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner.

Your responsibilities:

• Perform and review analytical testing (routine non-routine method validation and technical transfer) ensuring compliance with ICH CFR USP and EP guidelines.
• Validate and maintain laboratory equipment including calibration troubleshooting and qualification (IQ/OQ/PQ) for cGMP use.
• Prepare and review documentation such as SOPs work instructions test methods and validation protocols in line with company policies and regulatory standards.
• Train and support QC analysts deputize for the QC Team Leader and actively contribute to QC group activities.
• Ensure timely review and approval of test results manage deviations/non-conformances and maintain compliance with product license commitments and cGMP.
• Stay updated on analytical technologies and regulatory standards anticipating future requirements for continuous improvement

Qualifications and requirements:

• A third level qualification in a scientific/technical discipline required.
• A minimum of 2 years experience in a laboratory-testing environment within the biological and/or pharmaceutical industry.
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
• Demonstrated knowledge and testing experience in an FDA/IMB approved QC laboratory.

At Johnson & Johnson we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear fair and respectful of your time.

Heres what you can expect:

• Application review: Well carefully review your CV to see how your skills and experience align with the role.
• Getting to know you: If theres a good match youll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
• Staying informed: We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
• Final steps: For successful candidates you will need to complete country-specific checks before starting your new role. We will help guide you through these.

Required Skills:

Preferred Skills: