×
Register Here to Apply for Jobs or Post Jobs. X

Quality Control Sample Coordinator

Job in Durham, Durham County, North Carolina, 27703, USA
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.
Requirements:
  • 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.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary