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Full-Time

QC Specialist

Equipment Management I

Posted on 6/18/2024

Legend Biotech

Legend Biotech

1,001-5,000 employees

Develops and commercializes cell therapies

Biotechnology
Healthcare

Mid

Bridgewater Township, NJ, USA

Onsite position.

Category
Lab & Research
Medical Research
Required Skills
Communications
Management
Requirements
  • Minimum of Bachelor's or equivalent University degree required
  • Minimum three (3) years of relevant work experience
  • Experience in a Regulated Quality environment and/or Engineering Equipment Development environment
  • Experience with IQ, OQ, and PQ
  • Capability to creatively problem-solve and troubleshoot, develop improvement ideas, and independently implement associated solutions with minimal guidance as a proactive change agent.
  • Excellent written and verbal communication skills with the ability to communicate clearly and concisely with all levels.
  • Experience with equipment purchase, CSV, metrology, calibration, and/or maintenance
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory.
  • Experience developing content for Validation Life Cycle documents (e.g., Master Validation Plan, User Requirements, Design Specification, Test Protocols (IQ/OQ/PQ), Test Summary Reports, Data Integrity Assessments, and/or Traceability Matrix)
Responsibilities
  • Develop User Requirement Specifications (URS) and oversee the management of equipment qualifications.
  • Provide support for data integrity assessments within the laboratory.
  • Take the lead in managing Equipment Lifecycle Management processes, including overseeing change control procedures.
  • Document and manage records for corrective and preventative actions, ensuring compliance with regulatory standards.
  • Draft, review, and approve Standard Operating Procedures (SOPs) for equipment operation.
  • Conduct regular reviews of system audit trails / periodic review to ensure data integrity and compliance.
  • Manage equipment access rights and perform periodic reviews to maintain security protocols.
  • Maintain high level of familiarity with GMPs, CFR Part 11, and current regulatory guidelines related to instrument calibration and CSV (e.g., GAMP 5, USP <1058>, 21 CFR Part 210/211, etc.)
  • Utilize troubleshooting skills to address and resolve issues related to analytical equipment functionality.
  • Provide support during both internal and regulatory audits, ensuring adherence to established procedures and guidelines.
  • Collaborate with Quality Systems, IT, and site facilities to support ongoing instrument and applications troubleshooting, maintenance, retirement, and change management.
  • Interact with QC Analysts to nurture open dialogue regarding equipment metrology, maintenance, calibration, and repairs.

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

97%
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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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