Procurement Operations Specialist, Corporate Functions (Contractor)
PharmaBiotechQuality Assuranceemacroinformsapaws
Job description
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.Legend Biotech is seeking a Procurement Operations Specialist, Corporate Functions (Contractor) as part of the Procurement team based in Bridgewater, NJ. Role Overview
The Procurement Operations Specialist (Pipeline) role serves as first-line “procure-to-pay” (P2P) support for her/his supported business function, supporting and escalating Procurement-related payment, contracting, policy and approval-related issues to Functions/Stakeholders as appropriate. Key Responsibilities Receive/validate order information from Procurement/business function in order to facilitate creation of purchase requisitions PR When applicable, notify Procurement of planned contracts (for example, work orders or change orders) Confirm following: Budget availability; contract status (if applicable); applicable cost center; GL account; other relevant information Create (or revise, as applicable) PR, confirm PR creation with Procurement and stakeholder
Track PR approval flow
Relay PO# to Procurement and stakeholder once created
Coordinate with Accounts Payable invoices; create/distribute service entry sheets (SES)
Confirm services satisfactorily completed with stakeholder in writing
PR/PO/invoice/SES troubleshooting & dispute resolution
Confirm new suppliers created in S4
Identify recurring errors and process bottlenecks, recommend improvements, and support maintenance of procedures and P2P training modules.
Maintain transaction records and supporting documentation and support audit information requests.
Prepare monthly tracking reports covering PR/PO status, balances, aging items, and outstanding issues.
Identify potential duplicate requests or POs and escalate for review.
The role makes routine transactional decisions within approved procedures, assigned system access, and delegated authority. It identifies missing information, follows up on requests, and escalates exceptions to the appropriate process owner. Budget approvals, contractual commitments, policy exceptions, and payment authorization remain with the designated authorized owners. Requirements Bachelor’s degree from an accredited university.
1 – 3 years related Procurement or Supply chain experience in a similar role
Pharmaceutical industry experience
Ability to manage multiple requests, prioritize competing deadlines, maintain accurate records, and collaborate across business functions.
Extensive experience using SAP and Ariba modules
Advanced Proficiency of Excel- Pivot tables, macros, etc. #Li-MP1
#Li-ContractPlease 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.
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Associate Director, Strategic Planning
Eversana — Chicago, us
Associate Manager, Market Access & Pricing
Eversana — Toronto, ca
Medical Science Liaison/Senior Medical Science Liaison - Immunology and Gene Therapy - West
Eversana — Sacramento, us
Specialty Pharmaceutical Representative - Women's Health - Upper Manhattan Territory
Eversana — New York, us
Diagnostic Specialist - Appalachia
Eversana — Nashville, us
Shipping Associate - 3:30pm -12:00am
Eurofins — Louisville, us