Senior Materials Requirements Planner
Senior Materials Requirements Planner
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1 Vacancy
Job Description
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at
Job Function:
Supply Chain PlanningJob Sub Function:
Production Planning & SchedulingJob Category:
ProfessionalAll Job Posting Locations:
Malvern Pennsylvania United States of AmericaJob Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for a Senior Materials Requirements Planner to be located in Malvern PA.
Purpose: Be a part of the Clinical Supply Chan end to end (E2E) Planning organization and help us achieve our mission of delivering hope in a box to our patients. The Senior Materials Requirements Planner (MRP) is a site-based role responsible for the coordination and execution of activities related to the planning and procurement of raw materials and components to support clinical manufacturing throughout our global network of pilot plants across different modalities such as biologics advanced therapies and cell banking. Working in a dynamic environment that is a clinical supply chain the Senior Lead Materials Requirements Planner is expected to support projects that are aimed at optimizing and maturing our E2E Clinical network as well as activities within the MRP space.
You will be responsible for:
- Reviewing purchase requisitions and exception messages driven by both a system-based and manual demand intake process as a result of changes within the Clinical Master Production Schedule and/or Cell Bank development changes.
- Ensuring orders are placed in alignment with supplier lead times and maintain optimal inventory levels based on the desired level of flexibility within clinical supply chain.
- Running scenarios and providing decision matrix on order placement to E2E planning team (Supply Network Planner E2E Planner Clinical Supplier Integrator MCO and CMC Lead) when required.
- Liaising with supplier to clarify potential plan constraints and partner with Global Procurement Supply Network Planning and Malvern Clinical Operations until issues are solved.
- Ensuring material is delivered and released on time to successfully complete the production plan including additional expedition of new materials due to aggressive First In Human Trial timelines.
- Managing potential abrupt deviations to the plan by assessing with suppliers the feasibility of the changes rapidly highlighting to the affected internal partners if the changes are not possible.
- Providing material feasibility assessments as input into API Clinical Sourcing Committee indicating if request are feasible and constraints along with resolution scenarios.
- Tracking and reporting site level supplier service performance communicating the information to the relevant parties.
- Managing fast tracked introduction of new materials including activities such as master data creation planning parameters ordering of qualification sample while providing clear communication to project partners.
- Partnering with warehouse staff to understand and adhere to space constraints managing inventory levels within agreed targets and proactively communicating any planning changes that will impact future storage strategies.
- Interfacing with QA and warehouse staff regarding rejected/defective materials making necessary physical arrangements with the supplier to ensure a prompt return of goods or disposal if needed.
- Participating in initiatives to improve business processes and tools.
Qualifications / Requirements:
Education:
- A minimum of a Bachelors degree is required preferably with a focus in Science Engineering Business Supply Chain Management or a related field. An advanced degree is preferred.
Experience & Skills:
Required:
- 3 years of relevant professional work experience (including manufacturing logistics planning) is required.
- Knowledge of supply chain planning principles is required.
- Strong planning and scheduling skills are required.
- Strong operational and data analysis skills are required.
- Ability to analyze data to identify and resolve exceptions aiming to minimize supply disruptions is required.
- Results-oriented sense of urgency is required.
- Ability to work in cross-functional and cross-cultural environments considering diverse perspectives and styles is required.
- Knowledge in Office applications (MS Excel MS Word MS PowerPoint) is required.
- Experience in GMP GCP GDP and/or quality management systems or processes is required.
Preferred:
- Demonstrated knowledge and understanding of clinical trials and clinical supply chain preferred.
- Knowledge of Biologics and Advanced Therapy manufacturing processes is preferred.
- Project and change management skills are preferred.
- Experience with ERP (SAP) and Advanced Planning Systems (OMP) is preferred.
- Supply chain certification (APICS/IBF) is desirable.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation.
#LI-Hybrid
Purpose: Be a part of the Clinical Supply Chan end to end (E2E) Planning organization and help us achieve our mission of delivering hope in a box to our patients. The Senior Materials Requirements Planner (MRP) is a site-based role responsible for the coordination and execution of activities related to the planning and procurement of raw materials and components to support clinical manufacturing throughout our global network of pilot plants across different modalities such as biologics advanced therapies and cell banking. Working in a dynamic environment that is a clinical supply chain the Senior Lead Materials Requirements Planner is expected to support projects that are aimed at optimizing and maturing our E2E Clinical network as well as activities within the MRP space.
You will be responsible for:
Qualifications / Requirements:
Experience & Skills:
Required:
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation please email the Employee Health Support Center () or contact AskGS to be directed to your accommodation.
Required Experience:
Senior IC
Employment Type
Full-Time
