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Quality Control Sample Coordinator
Job in
Durham, Durham County, North Carolina, 27703, USA
Listed on 2026-09-15
Listing for:
Merck & Co.
Full Time
position Listed on 2026-09-15
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
Job Title:
Quality Control Sample Coordinator
Location:
Onsite, Durham, NC
Shift: Monday - Friday (7 AM - 4 PM or 8 AM - 5 PM)
Duration: 7 months
Pay Rate: ***/hr - ***/hr
Responsibilities:- Oversight of QC in-process, release, raw material, and stability, and development samples, associated document management, and collection of data.
- Adherence to all GMP requirements, a proficiency in understanding of FDA/EMEA regulations, effective interactions/communication with Quality management, personal development, and support of investigations and inspections/audits.
- Manage sample tracking and the inventory system to track commercial and development samples.
- Generate sample submission forms for various testing facilities and process returned results.
- Collect sample forecasts to ensure lead time notice.
- Confirm testing was complete when sample invoices arrive.
- Follow/track international shipments, and alert logistics group of any customs clearance issues.
- Inspect incoming sample shipments and take necessary actions if samples do not comply with SOPs.
- Review and evaluate temperature data reports from temperature monitoring devices included with sample shipments.
- Execute protocols to support network stability, qualified material programs and pipeline product studies.
- Create and continuously improve sample management procedures and processes.
- Communicate with other departments and sites including Quality Assurance, Manufacturing and Facilities to address compliance issues and to implement corrective actions and to improve programs.
- Write and revise documents such as SOPs and technical reports.
- May support the Manager for activities related to training of employees, coordination of tasks, compliance with GMP, and identifying and implementing corrective and preventive actions.
- Support Stability sets and pulls including aliquoting and shipping during the study.
- Other related job duties as assigned.
- High School degree with 6 years related experience in a GMP Quality Control Laboratory or Associate's degree with 4 years related experience in a GMP Quality Control Laboratory or Preferred, Bachelors' degree in a relevant scientific concentration plus 2 years related experience in a GMP Quality Control Laboratory.
- Possess a strong understanding of the requirements of sample receipt and inventory management in a GMP laboratory.
- Excellent oral and written communication skills with strong technical writing experience required.
- Able to work independently and effectively within the group, within Quality, and across the site.
- Ability to work in both paper based and electronic laboratory information management systems.
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