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Lab Quality Control Inspector (R1065598) in Marietta, GA at IQVIA™

Date Posted: 4/13/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Marietta, GA
  • Experience:
    Not Specified
  • Date Posted:
    4/13/2019
  • Job ID:
    R1065598

Job Description

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health.  A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.



PURPOSE

The Lab QC Inspector applies quality control experience and knowledge of process review into practical quality solutions for the company.  The Lab QC Inspector evaluates, monitors, and systematically recommends corrective actions of procedures and processes.  Professionally conducts reviews with a high level of communication that yields quality results.



RESPONSIBILITIES

  • Provide Quality Control (QC) documentation support to operations.
  • Perform QC review of run binders, paperwork, report tables, data tables, and cut point determinations.
  • Actively participate in QC educational programs: in-house workshops, presentations on current QC issues and trainings.
  • Participate in QC and company staff meetings and discuss findings and recommendations for resolving non-compliance.
  • Work in conjunction with Q² Solutions operations and individuals to improve quality systems.
  • Manage all assigned quality control projects with minor assistance from coworkers and manager.
  • May track and report deviation trends to management.
  • Evaluate all systems for gaps, recommend actions, and professionally communicate to management the analysis to continually improve quality.
  • Demonstrate continuous self-motivated quality development
  • Complies with Company SOPs and participates in the implementation of new SOPs.


REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Knowledge of word-processing, spreadsheet, and database applications.
  • Knowledge of GLP regulations and guidelines and basic quality review techniques.
  • Strong interpersonal skills.
  • Excellent problem-solving skills.
  • Effective organization, communication, and team orientation skills.
  • Ability to initiate assigned tasks and to work independently.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  • Familiarity with common inferential and descriptive statistical methods and the interpretation of their results is preferred.
  • Ability to work on several projects at once while balancing multiple and overlapping timelines.
  • Ability to assess workload and suggest prioritization to senior staff.
  • Careful attention to detail and accuracy.
  • Must be computer literate.


MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelor’s Degree and 1 year of relevant experience in a quality / laboratory environment, including GLP and/or Quality Assurance experience; or equivalent combination of education, training and experience.

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PHYSICAL REQUIREMENTS

  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Regular sitting for extended periods of time.


Job ID: R1065598