L

LGC Group

Sells oligos, probes, primers, viral materials

Quality Assurance Associate

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Part-timeAlexandria, MN, USAIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • Strong organizational skills and attention to detail are required.
  • Effective written and verbal communication skills are required.
  • Ability to manage multiple assigned tasks and meet established due dates is required.
  • Ability to work independently on routine activities while recognizing when assistance or escalation is required is required.
  • Working knowledge and proficiency with Microsoft Office, particularly Outlook, Word, and Excel, is required.

Responsibilities

  • Assist with maintaining accurate and complete electronic and hard-copy quality files.
  • Support routing of documents for review, approval, revision, and archival.
  • Assist with formatting quality documents using approved templates.
  • Support periodic file reviews to identify missing, incomplete, or outdated records.
  • Escalate documentation discrepancies to the appropriate Quality Assurance team member.
  • Enter and update information in approved quality systems, spreadsheets, and databases.
  • Assist with maintaining administrative trackers for deviations, certificates of analysis (COAs), nonconformances, rework, corrective actions, training, document changes, and other quality activities.
  • Assist with compiling supporting documentation for quality events and investigations.
  • Support follow-up and closure activities by collecting records and maintaining action-item trackers.
  • Assist with production record organization and administrative review in accordance with established instructions.
  • Review entered information for accuracy and completeness.
  • Assist with maintaining organized electronic folders for metrics, reports, and supporting records.
  • Support temporary projects and other administrative quality activities as assigned.
  • Perform other duties as required or assigned by management to meet business needs.

Desired Qualifications

  • Previous experience in a regulated manufacturing, laboratory, medical device, biotechnology, or quality environment is desired.
  • Familiarity with quality records, document control, production records, technical writing of CAD design, and electronic quality systems is desired.
  • Experience maintaining spreadsheets, logs, databases, or administrative trackers is desired.
  • Familiarity with data integrity and good documentation practices is desired.

About the Company

LGC Group

Sells oligos, probes, primers, viral materials

LGC Group provides life sciences tools and solutions, including oligo components, probes, primers, and recombinant viral materials, plus proficiency-testing schemes for areas like food safety. Its products support detection and development in healthcare through mass spectrometry, immunoassays, and nucleic acid chemistry for vaccines, diagnostics, and therapies. The company differentiates itself with a broad portfolio and global testing services that help customers from diagnostics to vaccine development. Its goal is to improve healthcare outcomes and public safety by enabling accurate testing and high-quality scientific tools.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
London, United Kingdom
Founded
1841

Recently Posted Jobs

Explore more opportunities at LGC Group

See more jobs