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QC Sample Coordinator

Medasource

Durham (NC)

On-site

USD 10,000 - 60,000

Full time

7 days ago
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Job summary

An established industry player is seeking a Quality Control Sample Management Technician to join their dynamic team in Durham. This entry-level role offers an exciting opportunity to support quality control processes, ensuring the integrity of samples in a GMP environment. You will be responsible for the movement and documentation of QC samples, collaborating with various departments to address any issues. If you have a strong work ethic and enjoy working in a lab setting, this position could be your next career step. Join a forward-thinking company that values teamwork and continuous improvement.

Benefits

Medical insurance
Vision insurance

Qualifications

  • 1+ year experience in a GMP production environment.
  • Ability to wear PPE and work in a lab setting.

Responsibilities

  • Facilitate movement of QC samples and maintain chain of custody.
  • Document sample receipt and collaborate cross-functionally.

Skills

GMP production experience
Strong communication skills
Teamwork
Ability to work in a lab environment
Strong work ethic

Tools

LabVantage LIMS

Job description

This range is provided by Medasource. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$20.00/hr - $25.00/hr

Direct message the job poster from Medasource

Schedule: 4 10 hour shifts, Wed-Saturday. ~8AM-6PM, sometimes could be 7-5 or 6-4 depending on when samples are coming into the lab.

Start: ASAP

Responsibilities

The QC Sample Management Technician facilitates the movement of QC samples from Manufacturing to the QC lab maintaining sample chain of custody and GMP documentation.

  • Support the quality control team to provide sample collection 5 days a week when in operation.
  • Receive, inspect, and inventory reference materials and samples from external sources.
  • Document sample receipt, storage, and movement by making entries into LabVantage LIMS per internal sample chain of custody process.
  • Collaborate cross-functionally to address sample issues that arise from manufacturing, laboratories and/or the warehouse.
  • Provide feedback related to SOP, protocol and report generation related to Sample Management.
  • Support continuous improvement projects and SOP revisions by providing input into the process and support associated procedural updates.
  • Assist in reagent inventory and glassware cleaning as needed.
  • Perform other duties as assigned.

Basic Qualifications

  • At least one year of demonstrated relevant experience in a GMP production environment.
  • Strong oral and written communication skills.
  • Teamwork and strong interpersonal skills.
  • Ability to work in a lab environment which may include wearing appropriate PPE and other safety related equipment.
  • Experience working in a GMP environment.

Must haves:

  • Strong work ethic
  • Ability to work 4 10s Wed-Sat

Additional Skills/ Preferences

  • Previous experience working with LabVantage LIMS.

Additional Information

  • Tasks may require repetitive motion and standing for long periods of time.
  • 4 10-hour shifts, Wed-Sat
  • Occasional shift work when required within the lab.
  • Travel may be required during project phase.
  • Light to moderate lifting and carrying of objects which may include laboratory samples, equipment, and materials.
Seniority level
  • Seniority level
    Entry level
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Health Care Provider and Manufacturing
  • Industries
    Hospitals and Health Care

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Inferred from the description for this job

Medical insurance

Vision insurance

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