AdresseWondering what’s within Beckman Coulter Diagnostics? Take a closer look.
At first glance, you’ll see that for more than 80 years we’ve been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We’re building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you’ll see 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.
Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges.
TheQuality Control Supervisor for Beckman Coulter Diagnostics is responsible for the QC department as per the responsibilities listed in the job description.
This position is part of the Quality Control (QC) department located in Lismeehan, O'Callaghan's Mills, Co. Clare and will be an on-site role. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.
You will be a part of the QC Team and report to the Senior QC Manager. If you thrive in a multifunctional, leadership, fast paced role and want to work to build a world-class Quality Control organization—read on.
In this role, you will have the opportunity to conduct:
Deputy for QC Manager/Senior QC Manager, as required.
Supervise QC Biochemists and test schedule to support supply chain and real-time program requirements and manage out of specification issues to ensure timely disposition of product. Train QC team on procedures, test methods, cGMP and BHR compliance, performance management of team, coach & mentor team to include support of team Developmental Objectives.
Complete approval of OOS reports, Trending and Reporting of OOSs, Progression of corrective action and review and disposition of test results, as required.
Generate and/or approve change controls and deviation records and ERP system disposition of in-process tested batches; ensure laboratory analytical method meet FDA QSR requirements and guidance documents, ensure accuracy/currency of QC processes and procedures and co-ordinate of departmental metrics.
Management of departmental CAPAs and PARs/CIs and supervise departmental stock control and purchasing activities.
Departmental representative on company projects to include new product/analyser introductions and participation in departmental and cross functional events and Kaizens.
The essential requirements of the job include:
Bachelor’s degree in Chemistry, Biochemistry, Microbiology or other relevant technical field
5+ years’ experience in the field, ideally in a Laboratory role, within an FDA regulated industry
Strong verbal and written communication skills.
Strong people skills with the ability to motivate a team and achieve results through influencing others.
Demonstrated, disciplined, problem solving skills.
When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
If you’ve ever wondered what’s within you, there’s no better time to find out.
