Date Posted: 11/02/2026
Hiring Organization: Rose International
Position Number: 510137
Industry: Biotech/Healthcare
Job Title: Quality Control Microbiology Technician
Job Location: Frederick, MD, USA, 21704
Work Model: Onsite
Shift: Wednesday-Saturday day shift (7am-6pm)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 20.00
Max Hourly Rate($): 22.00
Must Have Skills/Attributes: GMP, MS Excel, MS Word
Experience Desired:
Knowledge of GMP, SOPs and quality control processes for commercial manufacturing (1-2+ yrs),
Experience in aseptic techniques and clean room operations (1-2+ yrs),
Knowledge of GMP, SOPs and quality control processes for commercial manufacturing (1-2+ yrs)
Required Minimum Education: High School Diploma or equivalent
Preferred Education: Associate’s Degree
**C2C is not available**
Job Description
Note: 4 days per week, 10 hour shifts Wednesday-Saturday day shift (7am-6pm)
Required Education:
AA Degree and 1+ years’ experience in Microbiology lab/Environmental Monitoring OR
HS Degree and 2+ years’ experience in Microbiology lab/Environmental Monitoring OR
Required Skills:
Experience in the application of microbiological techniques such as environmental air monitoring, water testing, surface monitoring
Experience in aseptic techniques and clean room operations
Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs.
Ability to pass vision exam for visual inspection
Knowledge of GMP, SOPs and quality control processes for commercial manufacturing
Proficient in MS Word, Excel, Power Point and other applications
Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
Ability to be flexible with schedule, and work overtime as needed
Summary:
We are seeking a highly motivated individual to join us as a QC Microbiology Technician in our new commercial cell therapy production center located in Frederick, MD. You will work with the Quality Control team in supporting our efforts in this exciting new area of cancer immunotherapy. This position provides Quality Control microbiological testing for clinical and commercial manufactured product, responsible for product testing, microbial growth promotion testing, utility testing and environmental monitoring.
Responsibilities:
The QC Microbiology Technician performs essential laboratory support functions to ensure the integrity of microbiological testing and environmental monitoring programs within a GMP-regulated manufacturing environment. Key responsibilities include:
Maintain laboratory areas in a clean, organized, and sanitized condition in accordance with established procedures and safety requirements.
Perform environmental monitoring and/or utility monitoring activities, including sampling of classified manufacturing areas, utilities, and support systems, as a primary job function.
Receive, inspect, quarantine, and appropriately store purchased microbiological media and supplies pending laboratory approval and release.
Monitor biohazardous waste accumulation and coordinate the safe removal and disposal of waste with qualified Environmental Health and Safety (EHS) personnel.
Support validation, qualification, development, and commercial manufacturing activities through execution of assigned microbiological and laboratory support tasks.
Maintain compliance with applicable GMP, safety, environmental, and company requirements while documenting activities accurately and contemporaneously.
Collaborate effectively with Quality Control, Manufacturing, Quality Assurance, and other site functions to support operational objectives.
Perform additional duties and special projects as assigned by management.
Ensure assigned responsibilities may be appropriately delegated to qualified and trained deputies when operational needs require. - **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
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