Lab Tech - I

Spectraforce Technologies

Frederick (MD)

On-site

USD 50,000 - 65,000

Full time

3 days ago
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Job summary

Spectraforce Technologies in Frederick, MD is seeking a Quality Control Technician I for QC Lab Support. The role supports sample management, logging in LIMS, and coordination with QC/QA teams. Typical shift is 4/10, Wed-Sat 3:00pm-2:00am, with a 12-month contract and potential extension. Cross-functional collaboration and adherence to GMP are essential.

Qualifications

  • Bachelor's degree in a related field or AA with 2+ years in QC/biopharma labs (FDA-regulated)
  • High School Diploma with 3+ years in QC/biopharma labs (FDA-regulated)
  • GMP knowledge and laboratory best practices preferred

Responsibilities

  • Receive and log samples in LIMS and coordinate transfers to internal/external labs
  • Process samples for release, stability testing, and retains
  • Label, store, and organize samples per procedures
  • Perform routine lab storage area cleaning and restocking
  • Support deviation/investigation activities and escalate issues
  • Provide updates during daily/weekly meetings
  • Participate in Lean Lab and Operational Excellence initiatives
  • Ensure compliance with safety, quality, and regulatory guidelines

Skills

Attention to detail
Interpersonal communication
Verbal and written communication

Education

Bachelor's Degree
Associate Degree
High School Diploma

Tools

Microsoft Office
Excel
Visio

Job description

Job Title: Quality Control Technician I - QC Lab Support

Location: Frederick, MD 21704

Duration: 12 Months (Possibility of extension depending upon business requirements and performance)

Swing Shifts: 4/10 (4 days x 10 hours/day) | Wed - Sat. 3:00pm - 2:00am

Reports to: Manager, Quality Control Lab Support

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

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:

  • 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
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