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Associate QC Chemist

Samsungbiologics · samsungbiologics.com
RockvilleEntry level1–3 yrs
Apply on Samsungbiologics’s site
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The job in short

An entry-level full-time Research Scientist role at Samsungbiologics in Rockville, asking for 1–3 years of experience. Skills mentioned: Audit.

Audit

Details

Found
29 d ago · posted 2026-08-20
Location
Rockville
Pay (as listed)
$67,072–$89,430 a year

Full description

Associate QC Chemist • Perform and document routine analytical, biochemical, and non-compendial testing of in-process, release, and stability samples in accordance with approved SOPs, test methods, and cGMP requirements. • Operate, calibrate, maintain, and troubleshoot QC laboratory instruments and equipment in a compliant and efficient manner. • Apply knowledge of cGMP, FDA regulations (21 CFR), ICH guidelines, and other applicable regulatory requirements to ensure laboratory compliance. • Review laboratory procedures and identify continuous improvement opportunities to enhance compliance, efficiency, and data integrity. • Author, revise, and maintain laboratory SOPs, protocols, and controlled documents as required. • Assist with laboratory investigations, deviation assessments, OOS/OOT investigations, root cause analyses, and analytical method troubleshooting. • Support critical reagent qualification and requalification activities. • Participate in analytical method qualification, validation, verification, transfer, and compendial method implementation activities. • Maintain accurate, complete, and contemporaneous documentation in accordance with ALCOA+ and data integrity principles. • Adhere to all laboratory safety requirements and actively support a safe working environment. • Serve as a trained Self-Inspection Auditor and participate in at least 25% of departmental self-inspection activities to support audit readiness and continuous compliance. Qualifications • Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline. • 1-3 years of experience in a cGMP pharmaceutical, biotechnology, or biologics laboratory environment. • Working knowledge of analytical and biochemical testing techniques and laboratory instrumentation. • Familiarity with FDA cGMP regulations, 21 CFR Part 210/211, data integrity requirements, and laboratory compliance practices. • Strong technical writing, problem-solving, and organizational skills. • Ability to work independently as well as collaboratively in a fast-paced QC laboratory environment. The anticipated salary range for this position in Maryland is $67,072 to $89,430 plus annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Benefits: · 13 paid holidays · Vacation time · 401K match · Medical, dental and vision benefits effective day one of employment

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