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QA Investigations Lead III

Legend Biotech CorpRaritan, NJ

$81,273 - $106,669 / year

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Overview

Schedule
Full-time
Career level
Senior-level
Remote
On-site
Compensation
$81,273-$106,669/year
Benefits
Health Insurance
Dental Insurance
Vision Insurance

Job Description

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.

Legend Biotech is seeking QA Investigations Lead III as part of the Quality team based in Raritan, NJ. 

Role Overview

 The QA Investigations Lead is responsible for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment. This includes supporting and approving manufacturing investigations, ownership of various department projects, and tracking of quality metrics while ensuring high quality and complaint product supply.

Key Responsibilities  

  • Support compliance activities for site Quality Operations in accordance with Legend standards, procedures and cGMPs.

  • Collaborate with site personnel to provide guidance and determine resolution for manufacturing issues.

  • Ensure accurate and timely maintenance and review of manufacturing investigations, CAPAs, change controls and complaints.

  • Review and approve manufacturing procedures.

  • Support regulatory inspections and audits by ensuring inspection readiness within facility.

  • Perform internal housekeeping audits.

  • Perform analysis on quality indicating data and identifying trends.

  • Provide oversight for trending of quality compliance metrics.

  • Job duties performed routinely require exposure to and handling of biological materials and hazardous chemicals.

  • Works in a collaborative team setting with quality counterparts that include Manufacturing Operations, Operations Technical Support, Maintenance, Supply Chain and Planning.

Requirements

  • A minimum of a Bachelor's Degree in Science, Engineering or equivalent technical discipline is required.

  • A minimum of 4 years relevant work experience is required. It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.

  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices.

  • Great attention to detail and ability to follow the procedures.

  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision.

  • Good written and verbal communication skills are required.

  • Ability to summarize and present results, and experience with team-based collaborations is a must.

  • Must be able to interpret problems and effectively determine appropriate resolutions that ensure compliance and minimize risk.

  • Must exhibit strong leadership skills and effectively develop others.

  • Ability to collaborate well with stakeholders, customers and peers.

  • Must exhibit strong decision-making ability and think creatively while maintaining compliance and quality.

  • Must be able to discern the criticality of issues and to communicate to management regarding complex issues.

  • Ability to manage conflict and issues that arise with internal or external customers.

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The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.

Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.

Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

Pay Range (Base Pay):

$81,273—$106,669 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

EEO Statement

It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.

Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.

For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

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FAQs About QA Investigations Lead III Jobs at Legend Biotech Corp

What is the work location for this position at Legend Biotech Corp?
This job at Legend Biotech Corp is located in Raritan, NJ, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Legend Biotech Corp?
Candidates can expect a pay range of $81,273 and $106,669 per year.
What employment applies to this position at Legend Biotech Corp?
Legend Biotech Corp lists this role as a Full-time position.
What experience level is required for this role at Legend Biotech Corp?
Legend Biotech Corp is looking for a candidate with "Senior-level" experience level.
What benefits are offered by Legend Biotech Corp for this role?
Legend Biotech Corp offers following benefits: Health Insurance, Dental Insurance, Vision Insurance, Disability Insurance, Life Insurance, Paid Holidays, Paid Vacation, Paid Sick Leave, Parental and Family Leave, 401k Matching/Retirement Savings, and Health & Wellness Programs for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at Legend Biotech Corp?
You can apply for this role at Legend Biotech Corp either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.