An exciting opportunity has arisen for a Senior QC Analyst within the Global Quality Large Molecule Analytical Sciences QC team. As a Senior Analyst, your primary duties will involve being part of the Quality Control Testing Hub at the state-of-the-art single-use multi-product biologics facility in Dunboyne, County Meath, Ireland.
The QC Senior Analyst will support new product introductions and conduct biological, chemical, and physical analyses using state-of-the-art laboratory instrumentation and computer systems at the new biotech facility.
The main responsibility is to support the Quality Control testing function, ensuring compliance with cGMP and corporate regulations. This role is critical within the Quality organization to establish the Laboratories as a hub for specialized analytical testing and to create value for patients.
Key Responsibilities
* Deliver results within tight timelines
* Collaborate effectively with team members and influence stakeholders
* Troubleshoot and resolve issues efficiently
* Promote continuous improvement and challenge the status quo
* Think proactively and logically under pressure
* Utilize lean tools to build team capabilities
* Support change management initiatives
* Coach team members to foster a continuous improvement mindset
* Communicate effectively and develop team capabilities
* Provide and receive constructive feedback
* Work independently and as part of a team
* Maintain flexibility and self-motivation
* Support diversity and inclusion initiatives
* Set and pursue stretch goals
* Identify and communicate risks
* Collaborate across networks and improvement teams
* Coordinate with Process Development and Manufacturing for product quality information
* Drive a safety culture of 'everyone owns safety'
Required Skills and Qualifications
* Degree in Science, Technical, Quality, or related field
* 1-2 years’ experience in biotech or pharmaceutical industry
* Excellent communication skills
* Understanding of cGMP requirements
* Ability to work independently and in teams
* Strong organizational and time management skills
* Knowledge of analytical methodologies
* Understanding of GMP, ICH, USP regulations
* Familiarity with continuous quality and process improvement tools (e.g., Lean, 5S)
* Ability to work cross-functionally and manage priorities
We operate at the forefront of science and technology in Ireland, committed to making a difference globally. Our Dunboyne site is a key biologics manufacturing facility, accelerating the development and delivery of medicines.
We value diversity and are an equal opportunity employer. Please contact our Talent Acquisition Advisor for support during the recruitment process. We offer flexible working options and encourage discussions about flexibility during your application.
If you are ready to innovate and meet unmet healthcare needs, please apply today.
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