Quality Engineer - GMP Operations
Job in
Frederick, Frederick County, Maryland, 21701, USA
Listed on 2026-08-07
Listing for:
Doist
Full Time
position Listed on 2026-08-07
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
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
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.
Company Benefits:- Medical, Dental, Vision, Paid Sick leave, 401K
- 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.
- 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.
- Experience with Building Management Systems (e.g., Siemens Desigo).
- Cell & Gene Therapy manufacturing experience is a plus.
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