Senior Scientist, Biochemistry (office-based Livingston, UK)

at  Q Solutions

Livingston, Scotland, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Nov, 2024Not Specified02 Sep, 20244 year(s) or aboveIndependence,Analytics,Technology,Communication Skills,Regulatory RequirementsNoNo
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Description:

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.

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/career

Responsibilities:

  • 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.


REQUIREMENT SUMMARY

Min:4.0Max:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

Chemical

Proficient

1

Livingston, United Kingdom