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Quality Control Technician I - QC Lab Support

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Onsite

Quality Control Technician I - QC Lab Support

Planet Pharma

Quality Control Technician I - QC Lab Support

Skills

Testing & QA

9 days ago

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Important information


Contract type:

Freelance / Contract

Location:

Frederick, MD, USA

Work mode:

Onsite

Published on:

16 October 2026

What they need


Role Execute tasks associated with sample management, shipment of samples, and other lab support QC functions, while interacting cross-functionally with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), and Corporate teams.

Responsibilities (include But Are Not Limited To)

  • Receive incoming samples, verify documentation, and log sample information into LIMS.
  • Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
  • Label, store, and organize samples according to established procedures and storage requirements.
  • Coordinate sample transfers to internal and external testing labs.
  • Perform routine cleaning, maintenance, and restocking of sample storage areas.
  • Collaborate with MM, QA, and other QC functions-including Corporate QC-to support requirements around sampling, testing, and disposition.
  • Manage and complete all shipping activities within QC functions.
  • Complete routine review of records, such as sample chain of custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
  • Assist with deviation and investigation activities as needed.
  • Provide updates during daily and weekly meetings.
  • Participate in Lean Lab and other Operational Excellence initiatives.
  • Comply with all safety, quality, and regulatory guidelines.
  • Perform other duties as assigned.

Basic Qualifications

  • Bachelors Degree OR
  • AA Degree and 2+ years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory OR
  • High School Degree and 3+ years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.

Preferred Qualifications

  • Strong knowledge in applying GMP in QC lab.
  • Exceptional attention to detail and ability to keep track of multiple ongoing projects
  • Proficient in Microsoft Office, Excel, Visio, and other related applications
  • Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
  • Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
  • Ability to be flexible with schedule, and work overtime as needed

The team will operate 7 days a week, with an extended, overlapping shift structure.

The max pay rats is 20.40/hr for this position

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