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Quality Engineer - GMP Operations

Dawar Consulting, Inc.
Posted 4 days ago, valid for 13 hours
Location

Frederick, MD 21703, US

Salary

$36 per hour

Contract type

Full Time

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Sonic Summary

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  • Our client, a leading company in biotechnology and gene therapy, is seeking a Quality Engineer - GMP Operations in Frederick, MD.
  • This long-term contract position offers a pay rate of $36 per hour on W2, along with various company benefits including medical, dental, vision, and a 401K plan.
  • The role involves providing quality engineering oversight for cGMP maintenance, validation, and equipment monitoring activities in both commercial and clinical manufacturing environments.
  • Candidates must have a Bachelor's degree and at least 2 years of experience in a pharmaceutical or FDA-regulated setting, with familiarity in cGMP maintenance and quality oversight.
  • Preferred qualifications include experience with Building Management Systems and knowledge of cell and gene therapy manufacturing.

Our client, a world leader in biotechnology and gene therapy, is looking for a “Quality Engineer - GMP Operations” based in Frederick, MD.

 

Job Duration: Long Term Contract (Possibility Of Extension)

Pay Rate : $36/hr on W2

 

Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

 

Provide Quality Engineering oversight for cGMP maintenance, validation, and equipment monitoring activities supporting commercial and clinical manufacturing. Ensure compliance with regulatory requirements by reviewing work orders, supporting qualification and validation activities, managing quality risks, and collaborating with cross-functional teams to maintain reliable facility, utility, and equipment performance.

 

Key Responsibilities:

  • Provide quality oversight for cGMP work orders related to critical equipment, facilities, and utilities.
  • Review and resolve equipment monitoring system (EMS) alarms to ensure uninterrupted manufacturing operations.
  • Support Commissioning, Qualification & Validation (CQV) and Computer System Validation (CSV) activities.
  • Collaborate with Manufacturing, Engineering, Quality Control, Supply Chain, and Product Development teams.
  • Monitor quality metrics, support investigations, and implement quality risk management activities.
  • Ensure compliance with cGMP, FDA regulations, and pharmaceutical quality standards.
  • Support validation, maintenance, calibration, and continuous improvement initiatives.

 

Qualifications:

  • Bachelor's degree with 2+ years of experience (or equivalent education/experience) in a pharmaceutical or FDA-regulated environment.
  • Experience with cGMP maintenance, calibration, and quality oversight.
  • Familiarity with CMMS systems (e.g., Maximo, BMRAM) and Equipment Monitoring Systems (EMS).
  • Knowledge of CQV, CSV, quality risk management, and GMP compliance.
  • Strong analytical, communication, troubleshooting, and problem-solving skills.

 

Preferred Qualifications:

  • Experience with Building Management Systems (e.g., Siemens Desigo).
  • Cell & Gene Therapy manufacturing experience is a plus.

 

 

If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com

 

 






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