Spectraforce Technologies
Job Title - Quality Control Technician I (QC Lab Support)
Work Arrangement
Fredrick, MD 21704, 100% Onsite (Laboratory Environment)
Shift & Schedule
Day Shift: 4 days O 10 hours
Sunday - Wednesday | 7:00 AM - 6:00 PM
Duration 12 Months
Role Overview The Quality Control Technician I - QC Lab Support is responsible for executing activities related to
sample management, sample shipment, and laboratory support
within the QC function. This role requires close cross-functional collaboration with
Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), Corporate QC , and other QC teams to ensure compliant and efficient laboratory operations.
Key Responsibilities
Receive incoming samples, verify documentation, and log sample information into
LIMS .
Support
sample receipt, processing, and aliquoting
for release, stability testing, and retain samples.
Label, store, organize, and maintain samples according to established procedures and storage requirements.
Coordinate
sample transfers
to internal and external testing laboratories.
Perform routine
cleaning, maintenance, and restocking
of sample storage areas.
Collaborate with
MM, QA, and QC functions , including Corporate QC, to support sampling, testing, and disposition activities.
Manage and complete
shipping activities
within QC functions.
Review and complete documentation, including
chain-of-custody forms, processing logs, logbooks , and other QC records.
Assist with
deviations and investigations
as needed.
Provide updates during
daily and weekly meetings .
Participate in
Lean Lab
and other
Operational Excellence
initiatives.
Ensure compliance with all
safety, quality, and regulatory
guidelines.
Perform additional duties as assigned.
Basic Qualifications
Bachelor's Degree , OR
Associate's Degree
with
2+ years
of experience in Quality Control or biopharma laboratories (FDA-regulated preferred), OR
High School Diploma
with
3+ years
of experience in Quality Control or biopharma laboratories (FDA-regulated preferred).
Preferred Qualifications
Strong knowledge of
GMP
application in a QC laboratory environment.
Exceptional
attention to detail
and ability to manage multiple priorities.
Proficiency in
Microsoft Office ,
Excel ,
Visio , and related applications.
Excellent
interpersonal, verbal, and written communication
skills in a collaborative environment.
Comfortable working in a
fast-paced , small company environment with shifting priorities.
Flexible with schedule and willing to work
overtime as needed .
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Shift & Schedule
Day Shift: 4 days O 10 hours
Sunday - Wednesday | 7:00 AM - 6:00 PM
Duration 12 Months
Role Overview The Quality Control Technician I - QC Lab Support is responsible for executing activities related to
sample management, sample shipment, and laboratory support
within the QC function. This role requires close cross-functional collaboration with
Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), Corporate QC , and other QC teams to ensure compliant and efficient laboratory operations.
Key Responsibilities
Receive incoming samples, verify documentation, and log sample information into
LIMS .
Support
sample receipt, processing, and aliquoting
for release, stability testing, and retain samples.
Label, store, organize, and maintain samples according to established procedures and storage requirements.
Coordinate
sample transfers
to internal and external testing laboratories.
Perform routine
cleaning, maintenance, and restocking
of sample storage areas.
Collaborate with
MM, QA, and QC functions , including Corporate QC, to support sampling, testing, and disposition activities.
Manage and complete
shipping activities
within QC functions.
Review and complete documentation, including
chain-of-custody forms, processing logs, logbooks , and other QC records.
Assist with
deviations and investigations
as needed.
Provide updates during
daily and weekly meetings .
Participate in
Lean Lab
and other
Operational Excellence
initiatives.
Ensure compliance with all
safety, quality, and regulatory
guidelines.
Perform additional duties as assigned.
Basic Qualifications
Bachelor's Degree , OR
Associate's Degree
with
2+ years
of experience in Quality Control or biopharma laboratories (FDA-regulated preferred), OR
High School Diploma
with
3+ years
of experience in Quality Control or biopharma laboratories (FDA-regulated preferred).
Preferred Qualifications
Strong knowledge of
GMP
application in a QC laboratory environment.
Exceptional
attention to detail
and ability to manage multiple priorities.
Proficiency in
Microsoft Office ,
Excel ,
Visio , and related applications.
Excellent
interpersonal, verbal, and written communication
skills in a collaborative environment.
Comfortable working in a
fast-paced , small company environment with shifting priorities.
Flexible with schedule and willing to work
overtime as needed .
#J-18808-Ljbffr