Quality Control Chemist
Job in
New Market, Frederick County, Maryland, 21774, USA
Listed on 2026-08-11
Listing for:
The Planet Group
Full Time
position Listed on 2026-08-11
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Quality Control Chemist
12 Month Contract
Location:
Frederick, MD Onsite - Shift flexibility preferred
• Wed-Saturday, 40 hours/week
• Time:
Day 3PM - 1:30AM EST
Requirements:
- Bachelor's Degree OR AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience
- OR High School Degree and 3+ years' experience in biotechnology or related field and Quality Control experience
- 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
- 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:
Experience in the biotech and/or pharmaceutical industry
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
- 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
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