Job Description
At Beckman Coulter Diagnostics, we are committed to advancing and optimizing the laboratory to move science and healthcare forward. Our culture celebrates backgrounds, experiences, and perspectives of all our associates.
We are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.
As a Senior Validation and Verification Engineer, you will lead and manage process validation activities in our Co. Clare facility.
Key Responsibilities:
* Develop and maintain site master validation plan, procedures, work instructions, and templates in line with corporate and regulatory requirements.
* Lead, integrate, and project manage validation tasks and develop strategies on all validation projects with multifunctional project teams.
* Provide guidance and support to all departments to ensure they understand and comply with the requirements of cGMP as applied to the validation program.
* Prepare, review, and execute site validation protocols and final reports ensuring compliance to all relevant corporate and regulatory quality and validation procedures/work instructions and standards.
Requirements:
* Bachelor's degree in chemistry, biochemistry, engineering, or other relevant technical field with a minimum 5+ years experience in a highly regulated (FDA desirable) healthcare or related environment.
* Or Master's degree with a minimum of 3+ years experience or Doctoral degree with 0-2 years experience.
* Managing change effectively to better serve customers in a busy environment, with demonstrated ability to multi-task and deliver to agreed timelines.
Preferred Qualifications:
* Analytical data analysis, e.g., Minitab.
Benefits:
* Pension Fund
* Performance Bonus
* Medical Aid / Health Care