QC Scientist - Raw Materials

Requirements

• BS in Chemistry, Biochemistry, or related scientific discipline
• Minimum 3 years of relevant pharmaceutical QC experience; wet lab experience required
• Hands-on experience with raw materials testing
• Experience with compendial and physiochemical testing (appearance, pH, wet chemistry)
• Experience with HPLC/UPLC, GC, and FTIR
• Ability to work with USP/NF, Ph. Eur., and JP general chapters and monographs
• Strong documentation skills and understanding of cGMP requirements
• Proficiency in Microsoft Outlook, Excel, and Word
• Authorization to work in the U.S. without sponsorship
• Strong organizational and time-management skills; familiarity with Lean principles
• Close attention to detail and commitment to data integrity (ALCOA)
• Strong troubleshooting and problem-solving skills
• Ability to work independently and collaboratively in a fast-paced environment
• Position is Full Time, Monday-Friday, 8am-5 pm. Candidates currently living within a commutable distance of Gaithersburg, MD, are encouraged to apply
• Excellent full-time benefits include:
• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holiday
• Yearly goal-based bonus & eligibility for merit-based increases
• Base Compensation: $31-$40 per hour based on education and experience
• Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Benefits

Additional Information

Eurofins PSS is seeking a QC Scientist to help launch and support a new raw materials testing facility. This role will perform testing in compliance with cGMP guidelines and support team leadership in a start‑up lab environment. Testing will include FTIR, HPLC, GC, and other analytical techniques. Training will take place in Gaithersburg, MD and Frederick, MD. Responsibilities include but not limited to: Perform raw materials testing per GxP, SOPs, protocols, and applicable compendial chapters/monographs Execute wet chemistry, chromatographic (HPLC/UPLC/GC), and spectroscopic (FTIR) analyses Accurately document testing activities using data capture forms, electronic notebooks, and logbooks Enter and evaluate data against specifications; identify and report abnormalities Troubleshoot instruments and perform basic equipment maintenance Own minor deviations, invalid investigations, simple change controls, and CAPAs; support major deviations Write and revise SOPs and associated documentation Perform logbook, data, and documentation review Support implementation of new methods, technologies, and processes Maintain laboratory organization using Lean / 6 Sigma principles, including inventory management, glassware washing, and sample receipt and disposal Work effectively within a team while managing multiple priorities

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