E2E Supply Planner

Johnson & Johnson Co.; United States; On-site; USD 94,000 - 152,000; Full time

Benefits offered by this job

Vacation leave

Sick leave

Holiday pay

Parental Leave

Job summary

Johnson & Johnson is seeking an E2E Supply Planner for Clinical Supplies to lead daily activities including packaging, labeling, assembling and shipping for clinical trials in the United States, maintain the supplies database, and ensure GMP and regulatory compliance.

You will develop end-to-end supply plans, coordinate with plants and trial teams, drive process improvements, and ensure on-time delivery of trial material while managing risk.

Qualifications

• Minimum of a Bachelor’s Degree in business or science is required.
• Minimum of 3 years of related experience is required.
• Experience with supply planning processes including inventory, planning and Lean principles is required.
• Experience with GMP and quality management systems is preferred.

Responsibilities

• Develop E2E supply plans for clinical compounds across trials.
• Identify assumptions for kit/DP/API supply through the cS&OP process.
• Create drug product and drug substance supply plans by aggregating clinical and non-clinical demand.
• Provide information to capacity planners and schedulers for constrained scheduling.
• Drive improvements of functional processes in line with strategy.
• Ensure timelines and performance metrics align with GMP and compliance.

Skills

Leadership

Communication

Analytical thinking

Problem solving

Education

Bachelor's degree in business or science

Tools

SAP R/3

ERP

OMP

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through 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 humanity.Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

Belgium R-109449, United States of America R-108785

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Job Function:
R&D Operations

Job Sub Function:
Clinical Supply Operations

Job Category:
Professional

All Job Posting Locations:
Horsham, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

Job 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 https://www.jnj.com/innovative-medicine

We are searching for the best talent for E2E Supply Planner.

Candidates must already have authorization to work in the country of employment. Immigration sponsorship and relocation support are not available for this position. Candidates authorized to work pursuant to a short-term status (e.g., F-1) who require future immigration sponsorship are not eligible.

Purpose: Plans and manages the day-to-day activities of Clinical Supplies department such as packaging, labeling, assembling and shipping of clinical supplies used in clinical trials. Responsible for the department's clinical supplies database records maintenance, protocol evaluation, coding of samples, and storage of approved materials. Complies to local regulatory and good manufacturing practices guidelines.

You will be responsible for:

• Develop E2E supply plans for clinical compounds Identify the underlying assumptions for Kit/DP/API supply plan through the cS&OP process.
• Develop optimal end-to-end drug product and drug substance supply strategies for compounds that minimize waste while meeting the timelines and needs of the Clinical Trial Material supply plans.
• Create drug product and drug substance supply plans by aggregating clinical demand across different trials as well as non-clinical demands, to ensure timely delivery, testing and release of clinical batches.
• Provide information to the Supply Network Capacity Planners and Plant Schedulers to allow constrained master and/or detailed scheduling of batches in the CSC supply network in line with the trial requirements and in line with critical raw material and component availability.
• Drive structured improvements of functional processes in line with business or operational strategy.
• Ensure portfolio timelines and business performance goals, objectives and metrics are achieved, including consistency with GMP guidelines and all other compliance requirements
• Lead and/or supporting cross-functional and cross-departmental projects to improve business process/tools.

Qualifications/Requirements:

• A minimum of a Bachelor’s Degree in business or science is required.
• A minimum of 3 years of related experience is required.
• Experience with several of the following supply planning processes: inventory management, supply chain management, supply planning, production planning, Lean and 6sigma, systems (OMP, SAP R/3 or ERP), other cross-functional supply chain processes is required.
• Strong leadership skills: Managing complexity, conflict, and ability to identify process gaps based on data or root cause analysis, ability to predict risk/impact of supply related processes are required.
• Excellent communication, negotiation and influencing skills, with the ability to communicate clearly and appropriately to all levels of the organization in both written & oral forms is required.
• The ability to work independently, multi-task and manage complexity is required.
• An innate aim to make the difference and achieve results is required.
• Continuous improvement in attitude and innovative thinking that will help see opportunities and related business needs is required.
• Insight into a clinical supply environment in a pharmaceutical industry, its characteristics and constraints and Q&C requirements is preferred.
• Experience with GMP and/or Quality management systems and processes is preferred.

Other requirements

- Focus on achievement and delivery of results with high sense of urgency

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 & 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, external applicants please contact us via https://www.jnj.com/contact-us/careers , internal employees contact AskGS to be directed to your accommodation resource.

If you are under 18 years of age you (the candidate) may need to obtain the necessary working papers or other documentation required by state law to start the assignment, as well as get a parent’s consent for the background check.

The anticipated base pay range for this position is :
$94,000.00 - $151,800.00

Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:

Vacation –120 hours per calendar year

Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year

Holiday pay, including Floating Holidays –13 days per calendar year

Work, Personal and Family Time - up to 40 hours per calendar year

Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child

Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year

Caregiver Leave – 80 hours in a 52-week rolling period10 days

Volunteer Leave – 32 hours per calendar year

Military Spouse Time-Off – 80 hours per calendar year

The compensation and benefits information set forth in this posting applies to candidates hired in the United States.

Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

For additional general information on Company benefits, please go to: https://www.careers.jnj.com/employee-benefits