What are the responsibilities and job description for the QC Analyst II position at Zachary Piper Solutions, LLC?
Job Description
Piper Life Sciences has several active openings for a QC Analyst I with a large biopharma company in Baltimore, MD. This role follows a 4-day, 20 hour work week model: Wednesday - Saturday, 2nd shift hours .
Responsibilities for the QC Analyst I include:
• Perform environmental monitoring (EM) testing of water, compressed air, and gas, and perform WFI sampling.
• Perform incoming inspection of raw materials and components and the sampling of raw materials.
• Perform TOC testing to support release of production equipment.
• Perform daily laboratory tasks, such as balance calibration checks, temperature chart monitoring, lab cleaning and maintenance, CSR duties, etc.
• Assist with trending, archiving, and maintaining water data.
• Perform various analytical testing procedures as per manufacturing/quality control batch records, stability protocols, raw material requests for testing, etc.
• Write, revise, and review SOP's and Testing Standards as necessary.
• Review, analyze, interpret and report data to enter results in LIMS
• Participate in investigations, CAPA, change control activities and other related studies.
Qualifications for the QC Analyst I include:
• 0-2 years of industry experience within a biotechnology, pharmaceutical, or life sciences organization
• Bachelor of Science in Biology, Life Sciences, or related degree is required
• General knowledge of aseptic technique and following SOPs within a GMP/clean room environment
Compensation of the QC Analyst I includes:
• Salary Range: $32 - $37 hourly, commensurate with experience
• Full Benefits: Medical, Dental, Vision, 401k, Shift Differential Pay
Responsibilities for the QC Analyst I include:
• Perform environmental monitoring (EM) testing of water, compressed air, and gas, and perform WFI sampling.
• Perform incoming inspection of raw materials and components and the sampling of raw materials.
• Perform TOC testing to support release of production equipment.
• Perform daily laboratory tasks, such as balance calibration checks, temperature chart monitoring, lab cleaning and maintenance, CSR duties, etc.
• Assist with trending, archiving, and maintaining water data.
• Perform various analytical testing procedures as per manufacturing/quality control batch records, stability protocols, raw material requests for testing, etc.
• Write, revise, and review SOP's and Testing Standards as necessary.
• Review, analyze, interpret and report data to enter results in LIMS
• Participate in investigations, CAPA, change control activities and other related studies.
Qualifications for the QC Analyst I include:
• 0-2 years of industry experience within a biotechnology, pharmaceutical, or life sciences organization
• Bachelor of Science in Biology, Life Sciences, or related degree is required
• General knowledge of aseptic technique and following SOPs within a GMP/clean room environment
Compensation of the QC Analyst I includes:
• Salary Range: $32 - $37 hourly, commensurate with experience
• Full Benefits: Medical, Dental, Vision, 401k, Shift Differential Pay
Salary : $32 - $37
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