Full-Time

Quality Compliance Manager

Confirmed live in the last 24 hours

Legend Biotech

Legend Biotech

1,001-5,000 employees

Develops and commercializes cell therapies

Biotechnology
Healthcare

Senior

Bridgewater Township, NJ, USA

Category
Public Health
Biology Lab & Research
Biology & Biotech
Required Skills
Data Analysis
Requirements
  • A minimum of a Bachelor’s Degree in Engineering, Science or equivalent technical discipline is required
  • A minimum of six (6) years of experience in Quality Assurance/ Quality Systems or Compliance
  • Experience conducting internal audits (self-inspection), including writing audit reports, writing observations, and follow-through of observation resolution
  • Experience in front room/ back room roles for external audits
  • Experience working with quality systems is required
  • People leader experience preferred
Responsibilities
  • Successfully support the implementation, execution, and improvement of the internal audit process.
  • Support the planning and execution of internal audits for all quality system areas for the manufacturing site; write audit reports, issue audit observations and follow-through to ensure satisfactory resolution and closure of each internal audit.
  • Coordinate front room/ back room activities for health authority audits and independent audits; manage audit responses and observation resolution.
  • Drive site compliance to regulatory, enterprise, and global requirements through building positive relationships across functions, to meet unified business objectives.
  • As required, run reports and conduct data analysis to support monitoring of key performance indicators; support the preparation of compliance data for the monthly CRB & quarterly QSMR presentations.
  • Fulfills the Quality System audit module site key user responsibilities - represent the Raritan site in global forums/ team meetings, mentor site users for audit process, and control access to any systems used to support audits/inspections.
  • Provide support to quality systems team, ad hoc, for activities such as annual product review, site risk register, or internal quality agreements.
  • Develops and delivers training for specific quality system topics, in both classroom setting and individual interactions
  • Support the creation, assessment and closure as needed of corrective actions, change controls, or audit actions related to the site
  • Ensures and maintains a state of inspection readiness.
  • Perform compliance walkthroughs as part of audit/inspection readiness activities to ensure that the site is an inspection ready state.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.

Legend Biotech develops and commercializes cell therapies aimed at treating serious diseases, particularly cancers like hematological malignancies and solid tumors. Their approach is technology agnostic, allowing them to explore various methods to find effective treatments. The company operates in the personalized medicine sector, focusing on discovering, developing, and bringing new therapies to market. They generate revenue through licensing and selling their therapies, including CAR-T therapies, which involve modifying a patient's own cells to combat cancer. Legend Biotech emphasizes transparency with investors, regularly updating them on financial results and business developments.

Company Stage

IPO

Total Funding

$146.4M

Headquarters

Franklin Township, New Jersey

Founded

2014

Growth & Insights
Headcount

6 month growth

15%

1 year growth

40%

2 year growth

102%
Simplify Jobs

Simplify's Take

What believers are saying

  • CARVYKTI® received FDA and European Commission approval for expanded use in multiple myeloma.
  • Legend Biotech is expanding R&D with a new facility in Philadelphia.
  • Collaboration with Multiply Labs aims to automate and improve cell therapy manufacturing.

What critics are saying

  • Increased competition from Amgen's Imdelltra could impact Legend's market share.
  • Expansion into new R&D facilities may strain financial resources.
  • Dependency on external technology through partnerships like MaxCyte could pose risks.

What makes Legend Biotech unique

  • Legend Biotech focuses on personalized cell therapies for hard-to-treat cancers.
  • The company is technology agnostic, exploring multiple platforms for effective treatments.
  • Legend Biotech's CARVYKTI® is the first BCMA-targeted CAR-T therapy approved for second-line treatment.

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