Quality Control Technician I

Frederick, MD, US • Posted 4 days ago • Updated 4 days ago
Contract W2
Contract Corp To Corp
Contract Independent
12 Months
Travel Required
Able to Sponsor
On-site
$20 - $25/yr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • LIMS
  • lab information management system

Summary

Quality Control Technician I

QC Lab Support · 100% Onsite (Lab Environment)

Role 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

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

AA Degree and 2+ years'''' experience working in Quality Control or biopharma laboratories, preferably in an FDA regulated laboratory

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-paced small company environment and able to adjust workload based on changing priorities

Ability to be flexible with schedule, and work overtime as needed

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: nexinfo
  • Position Id: JP00017124
  • Posted 4 days ago
Contact the job poster
HJ

Harsha Jakheriya

Recruiter @ NexInfo Solutions, Inc.
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