QC Analyst B7 II

We are a national staffing firm and are currently seeking a QC Sample Coordinator for a prominent client of ours. This position is located in Durham, NC.Details of the position are as follows:

• $27-30/hr to start!
• Monday-Friday
• This position is a 7-month assignment with the possibility of extension or conversion.

• Oversee QC in-process, release, raw material, stability, and development samples, including documentation and data collection.
• Manage sample receipt, tracking, inventory, submissions, and shipment activities in accordance with GMP requirements.
• Generate sample submission forms, process testing results, and confirm testing completion.
• Support stability studies, including sample sets, pulls, aliquoting, shipping, and temperature monitoring.
• Execute protocols supporting stability programs, qualified material programs, and pipeline product studies.
• Review incoming samples and temperature data to ensure compliance with SOPs and laboratory requirements.
• Maintain accurate records in paper-based and electronic laboratory information management systems.
• Write and revise SOPs, technical reports, and sample management procedures.
• Support investigations, audits, inspections, and corrective and preventive actions.
• Collaborate with Quality Assurance, Manufacturing, Facilities, Logistics, and other sites to address compliance issues and improve processes.
• Support employee training, task coordination, and continuous improvement activities.
• Follow all GMP, safety, quality, and regulatory requirements.

• Bachelor’s degree in a relevant scientific field with 2+ years of GMP Quality Control Laboratory experience preferred.
• Associate’s degree with 4+ years of relevant GMP QC Laboratory experience, or High School diploma with 6+ years of related experience, may be considered.
• Strong understanding of sample receipt, inventory management, and sample tracking in a GMP laboratory.
• Experience with stability programs, QC testing, and laboratory documentation preferred.
• Experience working with paper-based and electronic laboratory information management systems.
• Strong technical writing, documentation, and communication skills.
• Ability to work independently and effectively within a team and across departments.
• Knowledge of GMP requirements and FDA/EMEA regulations.