At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
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Job Function: Quality
Job Sub Function: Quality Control
Job Category: Professional
All Job Posting Locations: Ringaskiddy, Cork, Ireland
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.
Job Description
We are searching for the best talent to join us as a Quality Control Analyst – Bioassay at Janssen Sciences Ireland (JSI) in Ringaskiddy, Cork, Ireland.
Purpose
In this role, you will be responsible for carrying out Quality Control laboratory activities related to bioassay testing, laboratory utilities, and equipment in compliance with Good Manufacturing Practice (GMP). You will partner closely with cross‑functional teams to ensure QC testing activities are executed efficiently, compliantly, and in alignment with regulatory expectations and company quality standards. Through this work, you support product quality, regulatory compliance, and continuous improvement across the site. You will need to achieve and maintain competency in JSI laboratory methods, procedures, and bioassay technologies, and training other QC analysts when required. Environmental, Health & Safety compliance is essential - you will need to comply with the company’s Environmental, Health & Safety Policy, Safety Statement, associated EHS procedures, local legislation, and duties outlined in the site EHS Manual.
You will be
Performing routine and non‑routine analytical and bioassay testing, including method validation and technical transfer activities in line with ICH, CFR, USP, and EP guidelines
Executing validation, operation, maintenance, calibration, and troubleshooting of laboratory equipment and associated software
Writing, executing, reporting, reviewing, and approving IQ/OQ/PQ protocols to ensure equipment is qualified for cGMP use
Reviewing and approving laboratory test results (where appropriate) and ensuring testing and approvals are completed within agreed turnaround times
Writing and reviewing laboratory Technical Manuals (TMs), SOPs, and Work Instructions (WIs) in accordance with company policies
Managing non‑conformances and deviations accurately and in a timely manner, ensuring compliance with product licence commitments, cGMP, and company quality standards
Acting as an active member of the QC group by supporting team activities, communicating issues to the QC Team Leader and Manager, deputising when required, and contributing to future planning and continuous improvement initiatives
Qualifications / Requirements
A third‑level qualification in a scientific or technical discipline
A minimum of 2 years’ experience in a laboratory testing environment within the biological and/or pharmaceutical industry
Demonstrated knowledge and testing experience in an FDA / IMB‑approved QC laboratory
Knowledge of FDA and EMEA regulatory requirements applicable to biologics and/or pharmaceuticals
Strong written and verbal communication skills
Strong attention to detail, problem‑solving ability, and analytical thinking
Ability to work effectively in a collaborative, cross‑functional environment
A results‑and performance‑driven, adaptable, and flexible approach
Benefits
In addition to base pay, we offer the following benefits: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well‑being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit https://www.jnj.com/.
The anticipated base pay range for this position is: €42.400,00 - €67.965,00
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