Validation Specialist

Legendcareers
Raritan, NJ
On-site

Who this role is best for

Candidates with validation or manufacturing experience in biopharma with technical expertise in aseptic processing and equipment qualification will find this role in a regulated environment.

Best fit for

  • Candidates with validation or manufacturing experience in biopharma and technical expertise in aseptic processing and equipment qualification
    — “2 years of experience in validation or manufacturing/process/production engineer within the pharmaceutical/biopharma industry.”
  • Individuals who have executed process validation and addressed deviations in regulated settings
    — “Execute site validation activities to the current regulatory and site requirements and address deviations associated with those activities”

Things to consider

  • This role is based in Raritan, New Jersey, with no mention of remote flexibility
    — “JOB SITE: 1000 US-202, Raritan, NJ 08869.”
  • The position is likely full-time, as contractors are excluded from benefits
    — “These benefits are offered exclusively to permanent full-time employees.”

How to stand out

  • Emphasize prior experience with protocol generation and aseptic process validation in your resume
    — “Control Aseptic process validation and particle runs from protocol generation, training execution oversight and reporting.”
  • Highlight your ability to perform Quality Risk Assessments and support change control processes
    — “writing or supporting Quality Risk Assessments.”
  • Demonstrate your track record in managing cross-functional teams and vendor relationships
    — “Work cross-functionally across Technical Operations and interface with external vendors”
  • Showcase your experience with data analysis and evaluation in validation or process qualification reporting
    — “Support APQ/APQR site reporting with data analysis and evaluation”
  • Include examples of implementing raw material or packaging changes with process impact studies
    — “Implement packaging and labeling changes including related studies and validation activities.”
Pace · SteadyCollaboration · HighAutonomy · MediumDecision Impact · Team

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • executing site validation activities
  • supporting equipment process qualification
  • overseeing manufacturing visual inspection program
Typical background
Bachelor’s degree in Industrial Engineering, Manufacturing Engineering, Mechanical Engineering or a related field2 years of experience in validation or manufacturing/process/production engineering within the pharmaceutical/biopharma industry

Skills & requirements

Required

Process ValidationEquipment QualificationAseptic ProcessingWriting Or Supporting Quality Risk Assessments

Preferred

Data AnalysisProject Management

Stack & domain

Process ValidationEquipment QualificationAseptic ProcessingWriting Or Supporting Quality Risk AssessmentsCell TherapyCar-tTcr-tNK Cell-based TherapiesEmerging PlatformsMultiple Myeloma

About the role

Original posting from Legendcareers via Greenhouse

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

COMPANY: Legend Biotech USA, Inc

JOB TITLE:  Validation Specialist

JOB DUTIES: 

Execute site validation activities to the current regulatory and site requirements and address deviations associated with those activities including oversite of pre-validation and validation activities resulting from technical changes. Control Aseptic process validation and particle runs from protocol generation, training execution oversite and reporting. Support equipment process qualification and ensure consistency with process needs defined by Manufacturing or Tech Support. Support the investigation of validation/PQ/study challenges at Site. Support the establishment of KPI and own execution of routing CPV/OPV reporting. Support APQ/APQR site reporting with data analysis and evaluation. Provide technical assessments, rationales, and approval for engineering and process changes to meet regulatory requirements. Implement and evaluate raw material and consumable changes for process impact including but not limited to leachable/extractable studies and perform associated implementation studies. Implement packaging and labeling changes including related studies and validation activities. Oversee the manufacturing visual inspection program. Control the manufacturing control strategy and microbial control strategy. Assess change controls for validation impact. Establish key stakeholder relationships with internal and external stakeholders. Identify and escalate potential risk areas/shortfalls to ensure the process remains in a validated state. Work cross-functionally across Technical Operations and interface with external vendors to drive the design and implementation of automation platforms for cell therapy development and manufacturing.

MINIMUM JOB REQUIREMENTS:

Education Required: Bachelor’s degree in Industrial Engineering, Manufacturing Engineering, Mechanical Engineering or a related field.

Experience Required: 2 years of experience in validation or manufacturing/process/production engineer within the pharmaceutical/biopharma industry. 

Special Skills Required: process validation, equipment qualification, or aseptic processing; writing or supporting Quality Risk Assessments. 

JOB SITE: 1000 US-202, Raritan, NJ 08869. 

WORK HOURS: 9:00 a.m. to 5:00 p.m. 5 days 40 hr/wk

SALARY: $120,000 per year

TO APPLY: E-mail CV to: Attn. E McShane: talent.acquisition@legendbiotech.com.

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): $120,000—$120,000 USDPlease note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

Work Authorization & Employment Eligibility

Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.

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.

Source: Legendcareers careers (Greenhouse)

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