Sr. Quality Control & Sample Management Specialist

Stratacuity: Proven Scientific Placement; Bedford (MA); On-site; USD 75,000 - 95,000; Full time

Job summary

A leading recruitment firm in the scientific sector is seeking a Sr. Quality Control & Sample Management Specialist to ensure high-quality data generation within the Translational DMPK and Clinical Pharmacology team. The successful candidate will perform QC reviews of bioanalytical data, manage documents, and oversee the sample lifecycle across studies. Candidates should have a Bachelor’s degree, experience in pharma or biotech, and proficiency with LIMS. This role offers the opportunity to significantly contribute to compliance and efficiency in a dynamic environment.

Qualifications

• 5+ years QC experience in pharma, biotech, or CRO environments.
• Proficiency with LIMS and electronic notebooks.
• Strong understanding of GxP regulations.

Responsibilities

• QC review of bioanalytical data and study documentation.
• Manage and review scientific documents in SharePoint.
• Contribute to drafting and editing bioanalytical lab guidelines.

Skills

QC review of bioanalytical data

Attention to detail

Communication skills

Organizational skills

Education

Bachelor’s degree in a scientific or healthcare field

Tools

LIMS (LabVantage preferred)

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Sr. Quality Control & Sample Management Specialist

Our client is looking for an experienced QC and sample management professional to support high‑quality data generation within our Translational DMPK and Clinical Pharmacology team. This role ensures accuracy, compliance, and smooth sample lifecycle management across internal and external studies.

Responsibilities

• QC review of bioanalytical data (LC‑MS/MS, ELISA, qPCR) and study documentation from internal teams and CROs
• Manage and review scientific documents in SharePoint
• Format internal reports and provide templates to CROs
• QC review of packing slips, manifests, and critical reagent documentation
• Contribute to drafting and editing bioanalytical lab guidelines
• Routine QC of Electronic Lab Notebooks
• Audit finalized reports and maintain errata
• Use LIMS (LabVantage) for sample receipt, tracking, aliquoting, storage, shipping, and disposal

Requirements

• Bachelor’s degree in a scientific or healthcare field
• 5+ years QC experience in pharma, biotech, or CRO environments
• Proficiency with LIMS (LabVantage preferred) and electronic notebooks
• Strong understanding of GxP regulations
• Excellent attention to detail, communication, and organizational skills
• Proficiency in Microsoft Word, Excel, and PowerPoint
• Familiarity with bioanalytical assays is a plus