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Dawar Consulting, Inc.

Dawar Consulting, Inc.

QC Chemist I

Frederick, USNa miejscuUmowaPełny etat

Opublikowano 30 wrz 2026

To stanowisko jest opublikowane w języku EN

Our client, a world leader in life sciences and biotechnology, is looking for a “QC Chemist I” based in Frederick, MD.


Job Duration: Long Term Contract (Possibility of Conversion to FTE)

Pay Rate : $30/hr on W2


Company Benefits: Medical, Paid Sick leave, 401K


Key Responsibilities

  • Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
  • Work with internal and external resources to maintain lab in an optimal state.
  • Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. Supply information to support generation of CoAs for product release.
  • Maintains laboratory instruments for calibration and routine maintenance
  • Author or revise SOPs, qualification/validation protocols and reports.
  • Monitor the GMP systems currently in place to ensure compliance with documented policies.


Qualifications

·       Bachelor’s Degree OR AA Degree OR High School Degree


Preferred Qualifications

·       Strong knowledge of GMP, SOPs and quality control processes.

·       Identifying, writing, evaluating, and closing OOS’s and investigations.

·       Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.

·       Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).



If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com





Przegląd stanowiska

Typ stanowiska

Pełny etat

Wymagane umiejętności

Cell-based bioassaysFlow CytometryELISA (enzyme-linked immunosorbent assay)qPCR / PCR assay techniquesGood Manufacturing Practices (GMP) complianceKnowledge of 21 CFR Part 11/210/211 regulatory requirementsAuthoring and revising SOPs, qualification and validation protocols/reportsInstrument calibration and routine laboratory maintenanceAnalytical data review, monitoring and trending for QC release (CoA support)Out-of-Specification (OOS) investigations and incident documentationLaboratory operations coordination with internal and external resources

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