QC Analyst

Sentior, Ltd.; Cork; Hybrid; EUR 34,000 - 55,000; Full time

Benefits offered by this job

Competitive hourly rate

Job summary

Johnson & Johnson Janssen Sciences Ireland (JSI) Cork seeks a QC Analyst to perform analytical testing in a GMP environment. You will support equipment qualification, calibration and troubleshooting, and collaborate with multiple departments to meet turnaround targets.

Required is a third level scientific qualification and at least 3 years in a QC lab, with knowledge of FDA/EMEA regulatory expectations for biologics or pharmaceuticals.

Qualifications

• Third level qualification in a scientific/technical discipline.
• Minimum 3 years of lab-testing experience in biological/pharmaceutical environments.
• Knowledge of FDA/EMEA regulatory requirements for biologics/pharma.

Responsibilities

• Carry out analytical testing activities to support GMP-related programs.
• Validate and transfer methods; write and review IQ/OQ/PQ protocols.
• Maintain equipment, calibration and troubleshooting; review data and reports.

Skills

Analytical testing

IQ/OQ/PQ protocols

GMP compliance

Education

Bachelor's degree in a scientific/technical discipline

Job description

HEALTHZZP toegestaan# QC AnalystJohnson & Johnson Cork 3 maandenGepubliceerd 1 dag geleden · Opportunity ID: 1061989Tarief indicatie —Uren 40 u/wStart 30 Nov 2026Duur 3 maandenInteresse in deze opdracht?## De opdrachtQC AnalystLocation: CorkDuration: 12 monthsHours: 39 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 mannerRoles and Responsibilities- Achieves competency in JSI laboratory methods and procedures.- Trains other QC analysts in laboratory methods and procedures when required.- Performs analytical testing activities in relation to method validation and technical transfer activities so as to ensure that all methods meet ICH, CFR USP and EP guidelines.- Executes validation, operation, maintenance, calibration and troubleshooting of equipment and its associated software.- Writes, executes, reports and reviews IQ/OQ and PQ protocols so as to ensure that all relevant equipment is qualified for cGMP use.- Performs routine and non-routine analytical testing activities.- Review and approval (where appropriate) of laboratory test results.- Ensures that testing and results approval are completed within agreed turnaround times.- Writes and reviews laboratory TMs, SOPs and WIs as directed by company policy.- Ensures QC activities are carried out in compliance with product licence commitments, cGMP and company quality standards.- Is an active member of the QC group and provide assistance with other group activities as required and communicates relevant issues to the QC Team Leader and Manager.- Anticipates and plans for future requirements in the area.- Deals with non-conformances/ deviations in an accurate and timely manner.- Deputizes for the QC Team Leader as appropriate.- Maintains and develops knowledge of analytical technology as well as cGMP standards.- Bioassay testing and Cell Culture.How to Succeed- A third level qualification in a scientific/technical discipline required. - A minimum of 3 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. BenefitsThis role offers a very competitive hourly rate. This contract will run for 12 months.about Johnson & Johnson Innovative MedicinePatients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.Janssen UK: https://www.janssen.com/uk/Janssen Ireland: https://www.janssen.com/ireland/Application ProcessWe are looking to process the first round of applications within the next 2 working days.We do not accept applications via email. The pay rate for this role will depend on how you are paid. PAYE, LTD & Umbrella options are available. Diversity, Equity & InclusionFor more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.