QC Specialist, Lab Services, II/III

Posted 25 Days Ago
Be an Early Applicant
Raritan, NJ, USA
In-Office
84K-110K Annually
Mid level
Biotech
The Role
The QC Specialist is responsible for sample management, documentation, and ensuring compliance with cGMP in the QC laboratory. They prepare documents, manage samples, and support audits while working independently and collaboratively as a technical specialist.
Summary Generated by Built In

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 QC Specialist, Lab Services, II/III as part of the Quality team based in Raritan, NJ. 

Role Overview

The QC Specialist, Lab Services is responsible for sample management. The QC Specialist is encouraged to work independently on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support to resolve some sophisticated issues. He/ She will serve as technical specialist within job function. Thinks logically and acts decisively.

Shift (Alternates Weekly) 

  • Wednesday-Saturday 5:00pm-4:00am 
  • Thursday-Saturday 4:00pm-4:00am

Key Responsibilities  

  • Prepares and reviews documentation independently.
  • Responsible for QC sample and retain management.
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems.
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint) and lab management software system (LIMS).
  • Prepare documents and coordinate Sample shipment (internal and external shipments).
  • Review logbooks and/ or LIMs to align physical quantities of samples in freezers/refrigerators.
  • Periodic inspection and consolidation of retains.
  • Document and perform sample management related non-conformance investigations.
  • Document and handle corrective and preventative action records.
  • Supports internal and regulatory audits.
Requirements
  • A minimum of a Bachelor’s degree or higher.
  • A minimum of two (2) years related experience in medical device, biopharmaceutical, or pharmaceutical industry.
  • A degree in Biology, Biochemistry, Microbiology, Chemistry or related field.
  • Solid understanding of regulatory requirements, policies and guidelines.
  • Experience with Quality Control document reviews and regulatory inspection processes.
  • Working knowledge of Quality systems.
  • Experience in management of retain samples using electronic systems (eLIMS).
  • Candidates must be able to accommodate shift schedule. Shifts include weekend and evening work as required by the manufacturing process.
  • This position will be located in Raritan, NJ and may require up to 5% of travel.
  • This position will occasionally require to lift up to 20 pounds.

#Li-RP1

#Li-Onsite

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):
$83,711$109,870 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.

Skills Required

  • A minimum of a Bachelor's degree or higher
  • A minimum of two (2) years related experience in medical device, biopharmaceutical, or pharmaceutical industry
  • A degree in Biology, Biochemistry, Microbiology, Chemistry or related field
  • Solid understanding of regulatory requirements, policies and guidelines
  • Experience with Quality Control document reviews and regulatory inspection processes
  • Working knowledge of Quality systems
  • Experience in management of retain samples using electronic systems (eLIMS)
  • Ability to accommodate shift schedule including weekends and evenings
  • Ability to lift up to 20 pounds

Legend Biotech Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Legend Biotech and has not been reviewed or approved by Legend Biotech.

  • Fair & Transparent Compensation Pay is considered competitive for many roles, with base rates often described as good or above local industry averages. Feedback suggests posted figures for titles like Specialist, Scientist, and certain HR roles sit above common national benchmarks.
  • Retirement Support A 401(k) company match that vests on day one is repeatedly highlighted as a standout element. Immediate vesting increases the tangible value of the retirement offering from the start of employment.
  • Leave & Time Off Breadth PTO structures commonly include vacation, personal, sick time, floating holidays, and around 11 company holidays. Several postings outline clear day allocations, signaling breadth and clarity in time-off design.

Legend Biotech Insights

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The Company
HQ: Somerset, New Jersey
1,192 Employees
Year Founded: 2014

What We Do

Legend Biotech is a global, commercial-stage biotechnology company developing and manufacturing novel therapies. We explore and apply innovative technologies to deliver cutting-edge options for patients around the world. Our corporate headquarters is located in Somerset, NJ, and our manufacturing footprint includes facilities in the United States, China and the Belgium.

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