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Salary
≈ $41k – $72k per year (Estimated)
Location
In office (United States)
Seniority
Junior
Employment
Contractor

Confirmed on the employer's own hiring board on Oct 26, 2026. First seen by Alion on Oct 12, 2026. Dawar Consulting scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Dawar Consulting is a staffing and professional services firm headquartered in Newark, California, in Silicon Valley, that provides contract, direct-hire and managed-services staffing alongside Workday HCM and ServiceNow implementation and support. Besides its California head office it has offices in Noida in India, Utrecht in the Netherlands and Mexico City, and its life science practice places scientists and lab staff with biotechnology and pharmaceutical clients on long-term contracts. Its openings are mostly client placements such as research associates, scientists, QC chemists, lab technicians and bioprocess engineers, plus SAP consultants and technical recruiters.

Our client, a world

leader in life sciences and biotechnology, is looking for a “Quality

Control Technician I” based out of Frederick, MD.

Job Duration: Long

Term Contract (Possibility Of Extension)

Company

Benefits: 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

    retains.

  • 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.

If interested, please

send us your updated resume at

[email protected] / [email protected]

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