Qa Rep

LSC have a great contract opportunity for QA Representative to join a leading Cork based pharmaceutical company.
ABOUT THE PROJECT - KEY RESPONSIBILITIES: Provide Quality leadership, direction, and governance for the specific areas of responsibility.
Manage quality-related matters specific to area of responsibility.
Responsible for approving appropriate quality-related documents.
Review and approval of other key GMP documents such as GMP standard operating procedures, raw material specifications, sampling protocols, master formulas, process flow documents Review and approval of GMP documents associated with qualification and validation including IQ/OQ/PQ & validation documents for facility, equipment, computer systems, GMP utilities, analytical methods, and processes, stability data, sampling protocols and Annual Product Reviews.
ABOUT YOU - ARE YOUR SKILLS A MATCH? Hons BSc, MSc, or Ph D in Pharmacy, Chemistry, Engineering, Quality, or related discipline, with a minimum of 2 years relevant experience.
Excellent attention to detail.
Experience working in cross functional teams and proven ability in decision making.
Demonstrates ability in critical thinking, data analysis, problem solving and experience in root cause analysis.
Understanding of Data Integrity and its applications Demonstrates a continuous improvement mind-set.
Demonstrated initiative - able to work proactively without direct supervision, continuous improvement mind-set.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1 G/Stamp 4 visa to apply Apply via this advert or contact Cian Marnane at if you have any more questions about this opportunity Skills: Documentation Validation Quality Assurance

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