Quality Control Technician I

Dawar Consulting; Frederick (MD); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Paid Sick Leave

401K

Job summary

Dawar Consulting is seeking a Quality Control Technician I in Frederick, MD, for a long-term contract in a GMP-regulated environment. The role involves managing sample receipt, processing, storage, and documentation, collaborating with various teams to ensure compliance.

Qualified candidates should have a Bachelor's degree or equivalent experience in QC or biopharma laboratories. Benefits include Medical, Dental, Vision, and 401K.

Qualifications

• Bachelor's degree OR AA degree + 2+ years OR High School diploma + 3+ years of experience in QC or biopharma laboratories.
• Knowledge of GMP and QC laboratory practices preferred.
• Strong attention to detail, organizational, and multitasking skills.

Responsibilities

• Receive, verify, log, process, and organize samples in LIMS.
• Coordinate internal/external sample shipments and manage QC shipping activities.
• Ensure compliance with GMP, safety, quality, and regulatory requirements.

Skills

Attention to detail

Organizational skills

Multitasking skills

Proficiency with Microsoft Office

Education

Bachelor’s degree or equivalent experience

Tools

LIMS

Job description

Quality Control Technician I

Frederick, United States | Posted on 05/30/2026

Our client, a worldleader in life sciences and biotechnology, is looking for a “QualityControl Technician I” based out of Frederick, MD.

Job Duration: LongTerm Contract (Possibility Of Extension)

CompanyBenefits: Medical, Dental, Vision, Paid Sick leave, 401K

Support Quality Control laboratory operations by managing sample receipt, processing, storage, shipment, and documentation in a GMP-regulated biopharma environment. Collaborate cross-functionally with QC, QA, Manufacturing, Material Management, and Corporate teams to ensure compliant sample handling and lab support activities.

Key Responsibilities:

• Receive, verify, log, process, and organize samples in LIMS for testing and retention.
• Coordinate internal/external sample shipments and manage QC shipping activities.
• Maintain sample storage areas, including cleaning, restocking, and organization.
• Review documentation such as chain of custody forms, logs, and lab records.
• Support investigations, deviations, and daily/weekly operational updates.
• Partner with QC, QA, MM, and other teams to support sampling, testing, and disposition activities.
• Participate in Lean Lab/Operational Excellence initiatives.
• Ensure compliance with GMP, safety, quality, and regulatory requirements.

Qualifications:

• Bachelor’s degree OR AA degree + 2+ years OR High School diploma + 3+ years of experience in QC or biopharma laboratories, preferably in an FDA-regulated environment.
• Knowledge of GMP and QC laboratory practices preferred.
• Experience with LIMS, sample management, and laboratory documentation.
• Strong attention to detail, organizational, and multitasking skills.
• Proficiency with Microsoft Office (Excel, Visio, etc.).
• Ability to thrive in a fast-paced environment with flexibility for changing priorities and overtime as needed.