Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.
Johnson & Johnson
IRL - QC Analyst - Normal
Job is closed
Posted
Dec 10, 2021
Job ID:
JJJP00009208
Location
Cork, County Cork
Hours/week
39 hrs/week
Timeline
1 year
Starts: Jan 10, 2022
Ends: Jan 8, 2023
Payrate range
Unknown
Application Deadline: Jan 10, 2022 12:00 AM
QC Analyst Bioassay - Days role
Job Description
Performs advanced tests and analyses to assure that products align with established specifications. Carries out complex calculations and documents test results. This is a volume driven position that that directly touches product. 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
Key Responsibilities:
? Attending daily meetings, working on own initiative.
? Testing and reviewing daily
? Training new analysts
? Always aim to meet site metrics
? Promoting 6S within the laboratories
Qualifications
Education:
A minimum of a bachelor?s degree in a science related discipline and 3 years of experience in a pharma company.
Experience and Skills:
? Cell culture experience necessary
? Cell bioassay and Process impurity testing experience required such as DNA, ELISA and HCP.
? Proficient in Lab report writing.
Job Description
Performs advanced tests and analyses to assure that products align with established specifications. Carries out complex calculations and documents test results. This is a volume driven position that that directly touches product. 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
Key Responsibilities:
? Attending daily meetings, working on own initiative.
? Testing and reviewing daily
? Training new analysts
? Always aim to meet site metrics
? Promoting 6S within the laboratories
Qualifications
Education:
A minimum of a bachelor?s degree in a science related discipline and 3 years of experience in a pharma company.
Experience and Skills:
? Cell culture experience necessary
? Cell bioassay and Process impurity testing experience required such as DNA, ELISA and HCP.
? Proficient in Lab report writing.
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