NEW JOB OPENING
QUALITY CONTROL TECHNICIAN - BIOPHARMA
IN Frederick, MD, USA!

 

Date Posted: 09/28/2026
Hiring Organization: Rose International
Position Number: 508286
Industry: Biotech/Healthcare
Job Title: Quality Control Technician - Biopharma
Job Location: Frederick, MD, USA, 21701
Work Model: Onsite
Shift: Wednesday to Saturday (7:00 AM-5:30 PM)
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 7
Min Hourly Rate($): 25.00
Max Hourly Rate($): 30.00
Must Have Skills/Attributes: Quality Control (QC)
Nice To Have Skills/Attributes: ELISA, Flow Cytometry, GMP, MS Excel, MS Word, SOP
Experience Desired: Working knowledge of quality systems and regulatory requirements (1+ yrs); Experience in the biotech and/or pharmaceutical industry (1+ yrs); Experience with QC, QA, Manufacturing and scientific/technical teams (1+ yrs)
Required Minimum Education: High School Diploma or equivalent
Preferred Education: Bachelor’s Degree

**C2C is not available**

 

Job Description
Shift Timings:

• For the first 7 weeks of the assignment, work Mon-Fri (07:30 AM-16:00 PM) to complete New Hire Orientation and Manufacturing On-boarding Technical Training.

• After the 7 weeks, the candidate is deployed to their agreed-upon shift. Wednesday to Saturday(7:00 AM-5:30 PM)



Required Qualification:

• High school diploma and 3+ years’ experience in biotechnology or a related field, and Quality Control experience



Preferred Qualification:

• Bachelor’s Degree OR

• Associate's Degree and 2+ years’ experience in biotechnology or a related field and Quality Control experience



Required Skills:



• 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).



Preferred Skills:

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

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

• Proficient in MS Word, Excel, Power Point and other applications.

• Strong written and verbal communication skills.

• Ability to communicate and work independently with scientific/technical personnel.

• Experience in the biotech and/or pharmaceutical industry



Responsibilities (include but are not limited to):



• 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.

• Assist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.

• Provide updates at daily and weekly meetings.

• Monitor the GMP systems currently in place to ensure compliance with documented policies.

• Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate.

• Gather metric information for use in continuous improvement of areas of responsibility.

• Perform other duties as required.

  • **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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About Rose

  • Founded in 1993
  • Office Locations Across the U.S.
  • 150+ Clients: Corporations and Government Agencies
  • Employee Oriented Company
  • Challenging Assignments Across the U.S.
  • Continuous Professional Development

Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.

David, Consultant

Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.

Diane, Consultant

Your team at Rose International is always very helpful and responsive.

Barbara, Consultant

My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.

Diana, Consultant

I believe the best thing that Rose HR has going for it is the incredible responsiveness. Everyone is very quick to reply to any concerns, and contacts the contracted employees very quickly and efficiently.

Kevin, Consultant

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