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 PhD 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 1G/Stamp 4 visa to apply!
Apply via this advert or contact Grainne Hodnett at +353 214771329 if you have any more questions about this opportunity!
