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Über
Remember to check your CV before applying Also, ensure you read through all the requirements related to this role.
If you have 3 years of experience working in the pharmaceutical industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT
- KEY RESPONSIBILITIES: QC Material Release & Scheduling Activities.
QC Key Performance Indicators.
QC Training
- Personal competency & Team development.
QC Documentation Review & Approval.
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.
ABOUT YOU
- ARE YOUR SKILLS A MATCH? Third level degree in a science or pharmaceutical discipline.
3+ years experience as a Micro QC Analyst.
Builds strong productive relationships.
Demonstrates ability to work with teams and individuals.
Holds self-accountable for compliant and flawless execution.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! xcfaprz Apply via this advert or contact Caoimhe O Sullivan at LSC on if you have any more questions about this role! Skills: QC Analyst Senior Quality Lab
Sprachkenntnisse
- English
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