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IQVIA Senior Scientist, Biochemistry (office-based Livingston, UK) in Livingston, United Kingdom

Job Overview

We are looking for a Senior Scientist to join Q2 Solutions , IQVIA’s laboratory business in Livingston, UK. The successful candidate will be responsible for serving as a technical specialist for laboratory operations, identifying and driving continuous process improvement initiatives.

Essential Functions

• Responsible for performing and documenting all analytical procedures with accuracy, consistency and timeliness in accordance with current standard operating procedures (SOPs) and regulatory guidelines.

• Performs routine and moderately complex data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.

• Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.

• Performs and documents hands on training for other Laboratory staff in areas of proven competency as assigned.

• Leads routine quality investigations. Assigns and completes CAPAs and effectiveness verifications.

• Oversees the technology transfer of methods and SOPs from other groups within Q2 Solutions.

• Collaborates cross-functionally to ensure assays will be sustainable and scalable in laboratory operations.

• Demonstrates advance knowledge to provide input on technical inquiries and provide leadership in troubleshooting projects, including root cause analysis and advanced problem solving.

• Produces analytical documentation for laboratory assays and associated pipelines across all service areas in the business (i.e. Laboratory Ops, Quality Systems, Information Technology, and Finance).

• Identify and lead continuous process improvement initiatives for laboratory operations, including but not limited to the following responsibilities:

• Review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives.

• Work with stakeholders on process improvement initiatives to present projects and ensure that goals are met.

• Independently identifies and evaluates vendor platforms to enhance delivery.

• Responsible for documentation of all project aspects including formal validations of laboratory methods.

• May present findings to a wide variety of audiences internal and external to Q2 Solutions.

• Shares accountability for lab documentation, ensuring SOP's are accurate by conducting regular reviews, updating as needed.

• Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.

• Prepares buffers and solutions for analysis, as required.

• Performs and documents calibration and maintenance of laboratory equipment as assigned.

• Responsible for producing high quality data and documentation in adherence to timelines in accordance with regulatory requirements.

• Participates in continuing education through self-study, attending in-services and off-site lectures and meetings and prepare programs to share with coworkers.

• Attends internal design calls and analytical assay review meetings to ensure effectiveness.

• May be responsible for contributing to the design and development execution of routine assays under moderate supervision.

• May act as a back up in any area of daily laboratory operations.

• Supports safety, quality, and 6S requirements and initiatives.

• Complies with company's procedures and applicable regulatory requirements.

Qualifications

• Bachelor's Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science,

medical laboratory technology or cytotechnology.) Req

• Typically requires >5 years experience in relevant discipline. Req

• >4 years of experience in a regulated laboratory. Req

• Sound knowledge of principles, theories, and concepts in job area.

• Knowledgeable across all assays within the scope of assigned technical area/dept.

• Working knowledge of applicable governing regulatory requirements.

• Strong knowledge of applicable lab techniques.

• Proficiency with laboratory calculations regarding batches and specimens including but not limited to averages, means, standard deviations, and various quality control metrics.

• Excellent oral and written communication skills.

• Strong organizational skills, and close attention to detail are essential.

• Capable of handling multiple tasks simultaneously and independently.

• Demonstrated “everyday leadership” skills.

• Ability to maintain a minor degree of independence to complete assigned tasks and projects.

• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

• Ability to synthesize information from various topics.

• Ability to bring projects and deliverables to completion under timeline expectations.

• This role is not eligible for UK VISA Sponsorship

Q² Solutions, IQVIA’s laboratory business, creates connected intelligence by combining our expertise, technology and analytics - this fuels unparalleled research & development solutions. We uphold a deep commitment to patients, sites, customers, and each other. https://www.q2labsolutions.com/careers

IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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