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Quality Assurance Specialist
Quality Assurance SpecialistRTD Biosciences • North Charleston, SC, United States
Quality Assurance Specialist

Quality Assurance Specialist

RTD Biosciences • North Charleston, SC, United States
7 days ago
Job type
  • Full-time
Job description

Company Description

RTD Biosciences LLC is a leading peptide manufacturing company focused on producing and distributing high-quality research peptides. Our mission is to deliver consistent and scientifically validated products that support innovation and research across various industries. Based in Charleston, South Carolina, we operate efficient fulfillment centers designed for timely delivery and exceptional client service. Through precision manufacturing and a customer-centric approach, we aim to empower groundbreaking discoveries and advancements.

Role Description

This is a full-time, on-site role located in North Charleston, SC. The Quality Assurance Specialist will be responsible for overseeing quality processes to ensure compliance with regulatory standards and company protocols. Daily tasks include performing quality audits, maintaining Good Manufacturing Practice (GMP) compliance, collaborating with the Quality Control team, and ensuring implementation of quality management systems. The specialist will also play an integral role in identifying, documenting, and resolving quality-related issues to maintain the highest levels of product integrity.

Qualifications

  • Proficiency in Quality Control and Quality Assurance practices
  • Knowledge of Quality Management systems and processes
  • Experience with Good Manufacturing Practice (GMP) guidelines
  • Ability to conduct Quality Auditing effectively and efficiently
  • Strong organizational, analytical, and problem-solving skills
  • Excellent attention to detail and commitment to accuracy
  • Bachelor's degree in Chemistry, Biology, or a related scientific field is preferred
  • Previous experience in the pharmaceutical or manufacturing industry is a plus
  • Proven experience in FDA and pharmaceutical regulatory environments.
  • Ability to train and coach staff effectively on new or revised SOPs and processes.
  • Certified Green Belt or Black Belt (Lean Six Sigma).
  • Experience working in an Aseptic Cleanroom environment.
  • CQA (Certified Quality Auditor) or CQE (Certified Quality Engineer) certification is preferred.
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Quality Assurance Specialist • North Charleston, SC, United States

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