Description
This position is responsible for carrying out tasks and projects related to equipment, lab utilities and testing procedures as required by GMP. Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner.
Duties and Responsibilities
Is an active member of the QC group and participates in the following key activities.
QC Material Release & Scheduling Activities.
QC Key Performance Indicators.
QC Training – Personal competency & Team development
QC Documentation Review & Approval
Site Cross Functional Team’s
Comply with EHS rules and procedures.
Delivers on the department Goals & Objectives & Continuous Improvement initiatives.
Support relevant internal and external site audits as required.
Maintains and develops knowledge of analytical methods, technology, and compliance demands.
Foster a culture of quality, safety, and compliance across the Site in line with the J&J Credo
Key Skills and Competencies Required
Builds strong productive relationships.
Demonstrates ability to work with teams and individuals.
Holds self-accountable for compliant and flawless execution.
Clear communication skills.
Innovative.
Always demonstrate Integrity and Credo-based actions
Education and Experience
Third level Degree in a science or pharmaceutical discipline.
A minimum of 3 years’ experience in a quality or compliance role within the pharmaceutical industry.
Skills
Microbiology
5 years
GMP
EHS
Material Release
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