Fresher Quality Assurance Jobs At Curia – Life Science Grads Apply Now
Curia is hiring a Quality Assurance Specialist I in Springfield, MO. This role offers the opportunity to work on the front lines of cGMP manufacturing operations, providing on-the-floor oversight, maintaining quality systems, and ensuring compliance with FDA regulations. If you’re looking to start or grow your career in quality assurance jobs within the pharmaceutical industry, Curia provides the training, benefits, and career advancement opportunities you need to succeed.
About the Company:
Curia is a leading global contract development and manufacturing organization (CDMO) with more than 30 years of experience serving pharmaceutical and biotech partners. With expertise across drug discovery, development, and manufacturing, Curia is dedicated to helping bring new therapies to market. Its mission is to transform ideas into life-saving treatments, improving patients’ lives worldwide.
Job Details:
- Job Details: Quality Assurance Specialist I
- Location: Springfield, MO, United States
Job Description
The Quality Assurance Specialist I is responsible for maintaining Quality databases and providing on-the-floor QA oversight to manufacturing operations. Key responsibilities include identifying compliance risks, managing corrective actions, and ensuring adherence to cGMPs.
Key Responsibilities:
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Maintain Quality databases, including archival and scanning of cGMP records.
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Represent QA during issues requiring immediate corrective action, ensuring documentation and compliance.
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Support investigations, deviations, change controls, and CAPAs.
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Author, review, and approve Quality Management System documents (SOPs, change controls, etc.).
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Perform QA visual inspections on clinical and commercial drug products.
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Assist in audits (internal, external, and client-related).
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Track Quality System metrics for management review.
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Partner cross-functionally to improve operational processes.
Qualifications:
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Bachelor’s degree in Life Science or related field (or equivalent GMP experience).
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0–3 years of experience in a GMP and FDA-regulated environment.
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Prior exposure to pharmaceutical or biotech quality systems preferred.
Why Join Curia?
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Generous benefits are effective on your first day.
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Paid training, vacation, and holidays.
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Career advancement opportunities with a global CDMO.
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Tuition reimbursement and learning platforms.
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401(k) program with company match.
Keywords: Quality Assurance Specialist, Curia, Pharmaceutical, Biotech, GMP, FDA, Springfield, Fresher Quality Assurance Jobs
