Senior Quality Control Scientist - United Kingdom - NeoGenomics

Description

Clinical LaboratoryBabraham Cambridge,United KingdomOnsite

Are you motivated to participate in a dynamic, multi-tasking environment? Do you want to join a company that invests in its employees? Are you seeking a position where you can use your skills while continuing to be challenged and learn? Then we encourage you to dive deeper into this opportunity.

NeoGenomics is looking for a Temporary Senior Quality Control Scientist at their Babraham, UK site. This is a temporary position for approximately three months for a Monday – Friday, day shift.

Now that you know what we're looking for in talent, let us tell you why you'd want to work at NeoGenomics:

As an employer, we promise to provide you with a purpose driven mission in which you have the opportunity to save lives by improving patient care through the exceptional work you perform. Together, we will become the world's leading cancer reference laboratory.

The Senior QC Scientist is responsible for the overall operation and administration of the reagent QC purchased and in-house manufactured reagents and consumables. The high complexity nature of the work requires knowledge about reagent QC testing, analytical NextGen Sequencing methods and technology, and regulatory requirements. This role will also contribute to the development of new products, new processes, and in ensuring the consistent quality of materials used in commercial patient sample testing within clinical laboratory.

• Establish a quality control organization within Laboratory Operations and build a team that will leverage both internal and external capabilities to enable both routine and unique QC testing needs for Inivata's IVD including continuous improvements.
• Collaborate with the Technology Transfer and Product Development team to develop Quality Control strategy and direction on new and existing analytical methods and provide support for verification, validation, and transfer activities.
• Responsible for investigation and resolution of reagent/consumable-related issue, including impact assessment, root cause analysis, and implementation of corrective and preventive actions and continual monitoring of its effectiveness.
• Troubleshoots and ensures corrective actions are taken whenever test systems deviate from the laboratory's established performance specifications.
• Responsible for ensuring reagent and consumable testing is performed and analyzed according to established manufacturing in a timely manner to support Lab Ops.

• BS, MS in Chemical, Physical or Biological Science or related filed 6 (Six) years of applied experience in demand planning, preferably in healthcare required
• Minimum of 4 years experience in an industry laboratory setting OR biochemical and molecular assays with demonstrated ability to analyse and problem solve complex issues impacting reagent performance.
• Minimum 1 year of leadership or mentorship experience in reagent manufacturing and/or quality control.
• Experience with next generation sequencing technologies (NGS) and molecular testing methods are highly desired.
• Advanced understanding of general laboratory techniques with emphasis on department specific techniques.
• Ability to make sound decisions under stressful situations.

All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status.