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Full-Time

Quality Compliance Lead

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 with a minimum of 4 of those within laboratories or laboratory oversight
  • 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
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 sells 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. Unlike many competitors, Legend Biotech emphasizes transparency with investors, regularly updating them on financial results and business developments. Their goal is to provide effective treatments for hard-to-treat diseases through innovative cell therapy solutions.

Company Stage

IPO

Total Funding

$750.5M

Headquarters

Franklin Township, New Jersey

Founded

2014

Growth & Insights
Headcount

6 month growth

20%

1 year growth

44%

2 year growth

101%
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Simplify's Take

What believers are saying

  • Legend Biotech's recent European Commission approval for CARVYKTI® positions it as a leader in the multiple myeloma treatment market.
  • Strategic partnerships, such as the one with MaxCyte, enhance Legend Biotech's capabilities in cell engineering and expand its technological reach.
  • The company's commitment to transparency and investor relations, demonstrated through regular financial updates, fosters investor confidence and long-term stability.

What critics are saying

  • The competitive landscape in cell therapy and personalized medicine is intense, requiring continuous innovation to maintain market position.
  • Regulatory hurdles and the need for extensive clinical trials can delay the commercialization of new therapies, impacting revenue streams.

What makes Legend Biotech unique

  • Legend Biotech's technology-agnostic approach allows it to explore multiple innovative therapies, unlike competitors who may focus on a single technology.
  • The company's comprehensive business model, from discovery to commercialization, ensures control over the entire treatment lifecycle, providing a competitive edge.
  • Legend Biotech's strong focus on CAR-T therapies, particularly for hematological malignancies and solid tumors, sets it apart in the personalized medicine sector.

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