Job Description
Quality Assurance Associate sought to support Biologics Manufacturing Facility in Limerick, Ireland, with expertise in Quality System compliance, digital technologies, and data analytics.
Lilly is a global healthcare leader headquartered in Indianapolis, Indiana, dedicated to discovering and bringing life-changing medicines to those who need them. Our employees around the world work to improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.
We are seeking a highly motivated, talented Quality Assurance Associate to support our new Biologics Manufacturing Facility. The ideal candidate is an organised and methodical professional who fosters a positive team environment.
Main Responsibilities:
- Build a state-of-the-art, digitally enabled QMS and ensure that the Quality System(s)/Program remains in a validated state and within regulatory commitments.
- Support the definition and implementation of Digital Plant systems and capabilities in the Quality Assurance, System and Compliance function.
- Assure consistent implementation of standards across the quality system.
- Manage quality-related matters specific to quality systems & compliance.
- Perform design and ongoing monitoring of relevant QA programs.
Key Skills and Experience:
- Minimum of 5 years' experience in GMP operations, IT management, or technology integration roles, preferably within the biotech or pharmaceutical industry.
- BSc (Level 8 Degree Minimum), MSc, or Ph D in Biotechnology, Chemistry, Engineering or related discipline with appropriate experience.
Additional Requirements:
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to work in a fast-paced environment and prioritize multiple tasks.