Sr Mgr, Quality Assurance
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| Job Type | Permanent |
| Area | Mayo, Ireland |
| Sector | Quality |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002663 |
| Job Views | 371 |
- Description
- Team Horizon is seeking a Sr Mgr, Quality Assurance for our client based in Mayo.Reporting to the Director of Quality, you will work with the Global Data Integrity group to develop appropriate Data Integrity programs/methodology, Standard Operating Procedures and practices and lead implementation of such in the facility.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Drive Data Integrity Quality Plans and Quality Improvement Plans based on gaps identified with short- and long-term mitigation plans defined
Report Data Integrity program status to the Global Team using appropriate tools and techniques to demonstrate progress as well as problems and solutions
Coach and mentor your team ensuring successful career development, a culture of continuous learning and encouraging an atmosphere of involvement, open communication and effective teamwork
Implement processes for monitoring systems data management and controls and maintain current data management systems (Lab Manager, iLab LIMs, MODA)
Implementing, qualifying, and maintaining data management software systems within the analytical and microbiology laboratories
Leading and supporting projects as part of Integration activities to align platforms across the Abbvie Network (Sample Manager)
What you need to apply:
Third level qualification in Engineering / Science
Minimum 3 years’ experience working in a regulated environment with people management experience.
Detailed knowledge of regulatory requirements in a pharmaceutical GxP environment
Ability to organize workload and work on own initiative.
Experience of working on a team, including strong organizational and time management skills.
Ability to learn new and different technologies.
Solution focused, with in-depth technical knowledge of both procedural controls and system controls for managing data Integrity.
Excellent documentation, organizational and prioritization skills.
Ability to effectively communicate plans, proposals, and actions at management levels.
Demonstrated problem solving skills, strategic thinking and ability to adapt to changing priorities
