Artificial Intelligence (AI), Communication Skills, Consulting, Corrective and Preventative Action (CAPA) Systems, Data Entry, Detail Oriented, Documentation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Healthcare, High School Diploma, Housekeeping/Cleaning, Laboratory, Laboratory Information Management System (LIMS), Laboratory Operations, Microsoft Excel, Microsoft Office, Microsoft Visio, Organizational Skills, Presentation/Verbal Skills, Quality Control, Regulatory Requirements, Safety Compliance, Short Messaging Service (SMS), Specimens/Samples, Test Lab, Writing Skills
Immediate need for a talented Quality Control Technician I – QC Lab Support | GMP | Sample Management. This is a 06+months contract opportunity with long-term potential and is located in Frederick, MD(Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID: 26-19172
Pay Range: $20/hr - $21/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment).
Key Responsibilities:
- Receive incoming samples, verify documentation, and enter sample data into LIMS
- Process, label, store, and organize samples according to established procedures
- Support sample aliquoting, receipt, retention, release, and stability activities
- Coordinate sample transfers to internal and external testing laboratories
- Manage QC shipping activities and maintain chain-of-custody records
- Perform routine cleaning, maintenance, and restocking of sample storage areas
- Review sample chain-of-custody forms, processing logs, logbooks, and related QC records
- Assist with deviations, investigations, and CAPA activities as needed
- Provide updates during daily and weekly team meetings
- Participate in Lean Lab and Operational Excellence initiatives
- Comply with all safety, quality, GMP, and regulatory requirements
- Perform other duties as assigned
Key Requirements and Technology Experience:
- Bachelor’s Degree
- Associate Degree with 2+ years of experience in Quality Control or biopharma laboratory work, preferably in an FDA-regulated environment, or
- High School Diploma with 3+ years of experience in Quality Control or biopharma laboratory work, preferably in an FDA-regulated environment
- Strong knowledge of GMP in a QC laboratory setting
- Experience with sample management, sample tracking, and sample shipment
- Working knowledge of LIMS
- Strong attention to detail and organizational skills
- Proficiency with Microsoft Office, Excel, Visio, and related applications
- Strong verbal and written communication skills
- Ability to work in a fast-paced, changing environment
- Flexibility to work overtime as needed
Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
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