QC Analyst

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.
 

We are currently recruiting a QC Analyst - (Bioassay) to join our contingent workforce on a growing team in Janssen Pharmaceuticals in Cork for an initial 12 month contract. 

About Janssen Pharmaceuticals:

Janssen Sciences Ireland UC, (previously Janssen Biologics), is part of the Johnson & Johnson family of companies, the world’s most comprehensive and broadly-based manufacturer of healthcare products and related services.  Our site in Ringaskiddy was established in 2005 on a 100-acre site with an investment of €500 million. We manufacture a range of biopharmaceutical products indicated for the treatment of conditions that include rheumatoid arthritis, psoriasis and cancer.  

We are expanding our site to allow us to meet the critical needs of patients around the world.  The expansion plans involve an investment of more than €300 million that will increase the existing manufacturing space by an additional 19,100m2, provide employment for up to 450 people during construction and an extra 200 people once completed.

Key Responsibilities:

• Performs advanced tests and analyses to assure that products align with established specifications. 
• Carries out complex calculations and documents test results. 
• Compiles and analyzes data on reoccurring product defects to determine root cause. 
• Documents analysis results. 
• Analyzes raw material inspection logs for consistent failures. 
• Notifies purchasing and quality departments about suppliers that have provided inferior products. 
• Studies work processes, measurements and performance metrics to identify improvement areas.
•  Recommends new or modified procedures based on findings. 
• Collaborates with customers, suppliers and associates to define and improve quality standards and expectations. 
• Participates on process improvement teams. 
• Monitors and scrutinizes internal and external complaints and compiles data to be used in reports. 
• Performs analyses in order to achieve compliance with specifications using a wide variety of chemical, biological and physical standard procedures
   

Candidate Requirements:

• A Bachelor's Degree in the relevant technical field.
• 12 - 18 months  industry experience in a QC Analyst role.
• Proven ability of working with teams, to quickly learn and understand complex topics
• Strong written and verbal communication skills, with a keen eye for detail
• Cell culture experience necessary
• Cell bioassay and Process impurity testing experience required such as DNA, ELISA and HCP.
• Proficient in Lab report writing.
   

If you meet our requirements and are interested in hearing more about our QC Analyst (Bioassay), please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!