Scientist I - Troubleshooting at QuidelOrtho
Pencoed, Wales, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

26 Aug, 25

Salary

0.0

Posted On

27 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

THE OPPORTUNITY

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic.
Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

SCIENTIST I

As QuidelOrtho continues to grow, we are seeking to appoint a Scientist I to join our Troubleshooting department in Pencoed on a permanent basis.

Responsibilities

YOUR NEW ROLE:

Reporting to the Technical Lead, the Scientist I role provides the opportunity to understand and develop skills in all aspects of the Product Support technical roles as part of a troubleshooting team. The successful candidate will be reporting into the Technical Lead and receive training in our investigation processes and gain an understanding of the nature of the work that the Tech Support Team are tasked with. We would also welcome new ideas, based on previous experience, to enable the team to be more effective and efficient. This role will work on a day’s basis Monday to Friday, with some weekend days’ work required which will be on a rotation basis between the team (Currently one weekend out of every four – days only).
Individuals will perform interpretation and analysis of scientific data and on occasion may take the opportunity to present data to an audience. They will ensure that investigations and projects are conducted in accordance with all relevant quality, compliance and safety systems and all quality documentation practises are followed.
As a Scientist I, you will work as part of a cross functional team, on a combination of short and long-term projects. Short term projects will revolve around reactive investigations, where you may work closely with R&D, Operations or Quality functions. Furthermore, you will lead longer term projects such as Cost Improvements and First Pass Approval Improvements which may arise from the reactive projects as CAPA investigations and implementations.
The role requires the ability to work well in a team and an individual contributor. The successful candidate will work independently to organise and plan their work but will also work closely with peers and Technical Leads. This is a great opportunity to apply your Product/ Process knowledge and further develop skills in teamwork, communication and working to fixed timelines.

WHAT YOU’LL BE DOING:

  • Day-to-day involvement with technical projects/investigations, which can include non-conformances, root cause investigations or projects which are necessary to support uninterrupted production in Operations or smooth transitions for new product introductions.
  • Responsible for all day-to-day ownership activities, including owning actions in cross-functional meetings, ownership/oversight of change notices and other quality documentation, where necessary conducting scientific (IA/IH) lab operations
  • Performing the interpretation, analysis, and documentation of scientific data
  • Providing conclusions and recommendations to the business, based on data extracted from the investigation/project/restock work and documenting according to QuidelOrtho record keeping practises.
  • Specialising in manufacturing processes such as wells, conjugate concentrates, buffers and in-house reference and selling material, will enable you to develop your knowledge further.
  • Complying to all GLP, GDP and EHS standards
  • Contributing to and coordinating continuous improvement of processes that operate within the group to provide consistently high levels of customer service.
  • Conducting the implementation of improvements as directed and remain open minded to innovative concepts and ideas.
  • This role will work in a lab environment 5-10% of the time only.
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