QC Analyst

QC Analyst 

Location: Cork

Duration:12 Months

Hours: Shift Cycle 

We have an exciting opportunity for a QC Analyst within Sample Management. The sample management team is dynamic, fast paced team within the QC Department, and is an area that faces continued growth year on year.  Responsible for the coordination and management of sample material from multiple sources to and from the QC department, the sample management team also have critical responsibilities in the areas of Reference Material and Customized reagent Inventory Management within QC. This is a volume driven position that that directly touches product. Handles testing samples and performs aliquoting of same. Manages inventory of all QC samples, retain and reference materials. Responds to requests from stakeholders for testing samples/reference materials. Plans and executes international shipments. Manages reference material and critical reagents. Receives raw materials into QC. Receives process gases to site. Ensures all activities follow SOP’s/WI’s and protocols where appropriate and are performed in compliance with regulatory guidelines. Studies work processes, measurements and performance metrics to identify improvement areas and recommend new or modified procedures based on findings. Collaborates with customers, suppliers and associates to define and improve quality standards and expectations. Participates in process improvement teams. Leads/take part in Quality Investigations. Completes GMP document updates.

Roles and Responsibilities

• Attending daily meetings, working on own initiative.

• Working on process improvements\

• Providing sample management and reference material handling for QC testing teams

• Training new analysts

• Always aim to meet site metrics

• Promoting 6S within the laboratories

• Use of laboratory software such as LIMS, SAP, SDMS, Trackwise, etc.

How to Succeed

• 3rd level qualification in a science related discipline. 

• Knowledge of laboratory sample management is preferred. 

• Industry experience (GMP laboratory) is essential. 

• Experience with LIMS systems is desirable.

Benefits

This role offers a very competitive hourly rate. This contract will run for 12 months 

about Johnson & Johnson Innovative Medicine

Patients 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 process

We 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 & Inclusion

For 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”.