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Salary
≈ $54k – $117k per year (Estimated)
Location
In office (Rockville)
Seniority
Junior · 1+ year exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 17, 2026. First seen by Alion on Aug 20, 2026. Samsung Biologics scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Samsung Biologics is a leading global CDMO providing end-to-end biologics development, CGMP manufacturing, and aseptic fill/finish services for biopharma partners worldwide.

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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