QA Lab Validation Specialist

2 weeks ago

Cork, Ireland Life Science Consultants (LSC) Full time

LSC have a great contract opportunity for a QA Lab Validation Specialist to join a Cork based Biotech Drug Substance Manufacturing Facility. This is an exciting opportunity to work with next-gen manufacturing technologies, advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction. If you have at least 5 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you ABOUT THE PROJECT - KEY RESPONSIBILITIES: Provide Quality leadership, direction, and governance for lab equipment and lab related systems. Investigate and troubleshoot issues relating to lab equipment and lab systems Manage Quality-related matters specific to area (Quality system or Quality Program) of responsibility. Approve appropriate quality-related documents. An approval signature confirms that site and GMP requirements have been met. Carry out day-to-day activities in compliance with site safety policies and procedures.? Promote and encourage safe practices and promptly report any safety concerns. Promote and encourage Quality culture and promptly report any compliance concerns. ABOUT YOU - ARE YOUR SKILLS A MATCH? May hold BSc, MSc or PhD in Chemistry, Engineering, or related discipline Experience working in cross functional teams and proven ability in decision making. Strong background in validation and compliance For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. Apply via this advert or contact Cian Marnane at if you have any more questions about this opportunity Skills: Lab Equipment Lab Systems Validation

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