Quality Control Scientist II — Genomics & Microbiology

LGC

Town of Middleton (WI)

On-site

USD 65,000 - 90,000

Full time

9 days ago
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Job summary

LGC Biosearch Technologies is seeking an Associate Scientist II, Quality Control to support and execute QC activities for microbiological and molecular workflows. The role interfaces with Manufacturing, Process Development, QA, and Operations to ensure product quality and compliance.

You'll perform routine QC testing, document results, and contribute to investigations and process improvements while adhering to ISO 13485 and quality system requirements.

Qualifications

  • Bachelor's degree in a relevant life sciences field with lab experience.
  • Experience executing laboratory workflows in regulated environments such as biotechnology or pharma.
  • Experience with microbiology, molecular biology techniques and aseptic technique.
  • Ability to interpret data and document results with good documentation practices.
  • Effective written and verbal communication and cross-functional teamwork.
  • Proficiency with Microsoft Office applications (Outlook, Word, Excel).

Responsibilities

  • Independently execute routine and moderately complex QC testing to support production schedules and product release.
  • Identify assay, documentation, and process improvement opportunities and contribute to change activities.
  • Perform tactical lab work, plan daily activities, and complete tasks with limited supervision.
  • Collaborate with QC, Manufacturing, Process Development, QA and Operations partners.
  • Document activities and summarize results, risks, and next steps to staff and leadership.

Skills

Attention to detail
Analytical mindset
Cross-functional collaboration

Education

Bachelor's degree in life sciences

Tools

Microsoft Office (Outlook Word Excel)

Job description

LGC Biosearch Technologies is seeking an Associate Scientist II, Quality Control to support and execute QC activities for microbiological and molecular workflows. The role interfaces with Manufacturing, Process Development, QA, and Operations to ensure product quality and compliance.

You'll perform routine QC testing, document results, and contribute to investigations and process improvements while adhering to ISO 13485 and quality system requirements.

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