The QC Inspector II inspects materials, parts and products at different stages of production. Performs quality control inspections, checks, and tests during the manufacture of products. Being a QC Inspector II requires a high school diploma or its equivalent. Records observations and may make recommendations for improving processes. In addition, QC Inspector II typically reports to a supervisor. Working as a QC Inspector II typically requires 1-3 years of related experience. May be entry level if some experience in the skill. Gains or has attained full proficiency in a specific area of discipline. Works under moderate supervision. (Copyright 2025 Salary.com)
Job Title: Quality Control Chemist
Location: Frederick, MD
Onsite
W2 Only (NO C2C)
Job Duration: 12 months
Job Description :
· Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
· 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.
· Asist with lab investigations regarding out of specifications (OOS) results. Participate in determination of root cause for deviations related to analytical procedures.
· 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.
Preferred Qualifications:
· 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.
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