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Laboratory Corporation of America Quality Control Technician (1st Shift) in Englewood, Colorado

Are you an experienced Medical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our Esoterix lab team as a Quality Control Technician in Englewood, Colorado. In this position you will work in a fast paced, customer focused, and challenging environment. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives".

Provides support in the secondary review of core and clinical trials project related assay documentation and raw data for accuracy, completeness and compliance with internal processes and procedures.

Job Duties/Responsibilities:

  • Reviews checklists for clinical trials data generated by technical staff for accuracy and completion of documentation, including review of supportive documentation as needed to ensure compliance with internal processes.

  • Provides review of QC change documentation generated by the QC lead.

  • Reviews data generated in study specific templates or spreadsheets used by technical staff to include check of manual calculations if applicable.

  • Assists in study test set up in LIS/Centerlinx: test code submission, sample requirements and/or review of data elements for submission.

  • Reviews study documentation binders to ensure proper documentation is in place during feasibility, validation and phase 1-111 studies (checklists, etc).

  • Notifies management of discrepant data or deviations observed in data review for clinical trials documents and assists with investigation and assigning root cause for deviations from internal procedures.

  • Communicates with laboratory technical staff to ensure data review findings are concurrent with established SOPs and proper documentation procedures.

  • Adheres to the standard operating procedures and safety requirements of Esoterix, CUA, CAP and other regulatory bodies.

  • Documents all activities as necessary including preventative maintenance logs, instrument function checks, troubleshooting, and quality control to ensure regulatory compliance

Requirements

  • Bachelor's Degree in a Life Science field of study or related scientific field

  • 1-2 years relevant QA/QC experience in pharmaceutical/biotech/laboratory industry or working knowledge of GLPs or FDA regulations. hghly preferred

  • Ability to work independently and within a team environment

  • Proficient with computers; Familiarity with laboratory information systems are a plus

  • High level of attention detail along with strong communication and organizational skills

  • Must be able to pass a standardized color vision screen

  • Flexibility to work overtime or other shifts depending on business needs

If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

Shift

1

Schedule

Monday-Friday 8:00a to 4:30p

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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