Senior Sample Management QC Specialist

QPS Holdings, LLC; Newark (DE); On-site; USD 49,000 - 57,000; Full time

Benefits offered by this job

401(k) matching

Life/AD&D Insurance

Disability Insurance

Park-like setting

Job summary

QPS Holdings, LLC in Newark, Delaware is seeking a Senior Specialist, Sample Management QC. This desk-based role focuses on document review, data verification, and system-based checks to ensure FDA and GLP compliance, without hands-on laboratory work.

The ideal candidate will have a degree in a relevant scientific discipline, experience in CRO or regulated environments, strong organizational and interpersonal skills, and proficiency with MS Office and LIMS software.

Qualifications

• Degree in a relevant scientific discipline or equivalent.
• Experience in CRO or other regulated clinical research environments preferred.
• Experience in FDA-related or regulated industry laboratory settings an advantage.
• Strong organizational skills and attention to detail.
• Proficiency with MS Office, including Excel, and basic data management tools.
• Good interpersonal skills with the ability to communicate across teams.

Responsibilities

• Create and maintain Sample Receipt notebooks from creation to archival.
• Use LIMS for tracking samples through their lifecycle at QPS.
• QC Sample Receipt records against electronic databases for FDA/GLP compliance.
• Ensure GLP paperwork accompanies sample receipt packets.
• Verify shipment receipts and reconciliations per client protocol.

Skills

Attention to detail

Organization

Multi-tasking

Interpersonal skills

Education

Degree in a relevant scientific discipline

Tools

LIMS software

MS Excel

Job description

QPS Holdings, LLC in Newark, Delaware is seeking a Senior Specialist, Sample Management QC. This desk-based role focuses on document review, data verification, and system-based checks to ensure FDA and GLP compliance, without hands-on laboratory work.

The ideal candidate will have a degree in a relevant scientific discipline, experience in CRO or regulated environments, strong organizational and interpersonal skills, and proficiency with MS Office and LIMS software.