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QC Specialist – Chemistry; Sample Management

Job in Norwood, Norfolk County, Massachusetts, 02062, USA
Listing for: JMD Technologies Inc.
Full Time position
Listed on 2026-01-11
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 40 - 45 USD Hourly USD 40.00 45.00 HOUR
Job Description & How to Apply Below
Position: QC Specialist – Chemistry (Sample Management)

QC Specialist – Chemistry (Sample Management)

Base pay range: $40.00/hr - $45.00/hr

Title:

QC Specialist – Chemistry (Sample Management)

Location:

Greater Norwood Area, MA (Onsite – Wednesday to Saturday, 6:00 AM–4:00 PM)

Status:
Accepting Candidates

About the role:

Join a growing Quality Control organization supporting Chemistry, Microbiology, Bioassay, and Raw Materials operations in a cGMP‑regulated environment. This role focuses on QC Sample Management leadership, daily operational coordination, and audit readiness in a fast‑paced life sciences setting.

Responsibilities:

  • Lead and coordinate QC Sample Management activities across Chemistry, Microbiology, Bioassay, and Raw Materials workflows.
  • Oversee daily sample schedules to ensure timely processing, compliant documentation, and completion of lab records.
  • Create weekly schedules and lead team meetings to align operational priorities and resolve issues.
  • Partner with Digital and IT teams to optimize LIMS (Lab Vantage) usage and expand QC data capabilities.
  • Support internal and external audits and maintain inspection readiness.
  • Author and revise SOPs, deviations, CAPAs, and change controls.
  • Lead investigations related to sample handling and compliance events.
  • Manage controlled temperature unit (CTU) systems, including monitoring and troubleshooting.
  • Support onboarding, training, and performance oversight of Sample Management staff.
  • Promote a strong culture of safety, quality, and compliance in the laboratory environment.

Qualifications:

  • BA/BS in a scientific discipline with 3–5 years of cGMP Quality Control experience, or MS with 1–3 years of cGMP QC experience.
  • Hands‑on experience in QC Sample Management within a regulated laboratory environment.
  • Strong working knowledge of LIMS (Lab Vantage preferred) and quality document systems (Veeva).
  • Solid understanding of FDA, EU, and ICH guidelines and regulations.
  • Experience with gowning, aseptic techniques, and general lab safety practices.
  • Ability to independently prioritize and manage multiple tasks in a fast‑paced environment.
  • Strong communication and people coordination skills.
  • Flexibility to support occasional on‑call, weekend, or holiday coverage as needed.

Compensation (MA Pay Transparency):

  • $40–$45/hr (W-2)
  • Final rate within the posted range depends on qualifications and interview outcomes.
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