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QC Technician| Laboratory Technician| $21/hr

$21 per hour

Lancesoft INC

Job Description

Job Description

Title:               Quality Control Technician I

Location:        9021 Bennett Creek Blvd, Maryland ,21704

Shift:              Wed - Sat. 3:00pm-2:00am

Swing Shifts: 4/10 (4 days x 10 hours/day)

 

Job Overview:

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:

  • Bachelor’s 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

Vacancy posted 2 days ago
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