QC Data Analyst

⭐ - Featured Role | Apply direct with Data Freelance Hub
This role is a QC Data Analyst for a 12-month contract at $23.00-$25.00 per hour, requiring a BS/BA in Chemistry or Biology. Key skills include data analysis and compliance, with preferred experience in a cGMP pharmaceutical environment.
🌎 - Country
United States
πŸ’± - Currency
$ USD
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πŸ’° - Day rate
200
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πŸ—“οΈ - Date discovered
September 11, 2025
πŸ•’ - Project duration
More than 6 months
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🏝️ - Location type
Unknown
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πŸ“„ - Contract type
Unknown
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πŸ”’ - Security clearance
Unknown
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πŸ“ - Location detailed
Troy, NY 12180
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🧠 - Skills detailed
#Databases #Data Analysis #Compliance
Role description
A well-established Biotech company is looking for an entry-level QC Data Analyst to support its team! These are all 12-month temporary roles, with strong potential for permanent hire. Great opportunity for recent graduates in the life sciences! Role Details: 12-month contract (potential for permanent hire) $23.00-$25.00 per hour M-F 8am-4:30pm A typical day might include: Act as a liaison between QC, Process Analytical Sciences, and Manufacturing group to provide trending analyses to support various activities such as manufacturing investigations, and validation studies. Assist in the implementation and maintenance of product release data trending program for each product candidate Write lot specific data trending reports for each lot to be released Prepare and populate matrices (databases, spreadsheets) designed to track testing and review status of release, lot release data, etc. Compile data to support QC department metrics and performance tracking Ensures compliance with applicable cGMP regulations and SOPs Meet specified timelines to support release and regulatory filings Complies with all pertinent regulatory agency requirements. Participates in required training activities. Trend QC product release data to support lot release and regulatory filings Education and Experience: Requires BS/BA in Chemistry, Biology or related field. Experience working in a cGMP pharmaceutical Quality Control Laboratory is preferred but not required. Or equivalent combination of education and experience. Nesco Resource provides equal employment opportunities and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. PRO062