LSC have a great contract opportunity for a QC Specialist to join a global Biopharmaceutical company in Carlow.
If you have relevant experience and a particular skill set in their area of expertise that adds value to the business; in a GMP setting and are ready for your next challenge, this could be the perfect project for you!
ABOUT THE PROJECT – KEY RESPONSIBILITIES:
o Work as directed by the Quality Control Manager / Associate Director, according to Company safety policies, cGMP and cGLP.
o Required to drive compliance with company Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
o Required to comply with company Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
o Develop, implement and maintain procedures that comply with appropriate regulatory requirements.
o Ensure that all Quality Systems within the department are adhered to on a daily basis.
o Operate as part of the QC team performing the allocated testing and laboratory based duties.
o Participate in method transfers and provide technical expertise and troubleshooting to support analysis.
o Ensure timely completion of all assigned data processing and reviewing.
ABOUT YOU – ARE YOUR SKILLS A MATCH?
o Bachelor’s Degree or higher preferred; ideally in a science related discipline
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!
To apply, submit your CV via this advert or contact Conor Dolan at LSC on 021-4777329 if you have anymore questions about this QC Specialist opportunity!