The role involves planning, organizing, and leading the effective operation of a production unit, including development projects, resource management, and personnel leadership.
Responsibilities
Plan, organize, and lead the effective operation of the production unit.
Lead and/or participate in development (equipment, processes, products) and efficiency improvement projects.
Ensure effective use of production resources and unit personnel management.
Participate in recruitment, organize employee training, and facilitate optimal use of staff knowledge and experience.
Prepare and submit unit budget plans to management and control expenditure.
Requirements
Augstākā izglītība
Nice to have: Experience leading a team of 50+ employees
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.
Locations (3)
Horsham, Pennsylvania, United States
Titusville, New Jersey, United States
Belgium
Compensation
The anticipated base pay range for this position is : $94,000.00 - $151,800.00
Responsibilities
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
Plans and manages day‑to‑day activities of Clinical Supplies department, including packaging, labeling, assembling and shipping of clinical supplies used in clinical trials.
Compensation
The anticipated base pay range for this position is: €61,200.00 - €98,210.00
Responsibilities
Develop E2E supply plans for clinical compounds
Identify assumptions for Kit/DP/API supply plan through cS&OP process
Develop optimal end‑to‑end drug product and drug substance supply strategies
Create drug product and drug substance supply plans by aggregating clinical demand
Provide information to Supply Network Capacity Planners and Plant Schedulers
Requirements
Bachelor's Degree in business or science
Nice to have: insight into clinical supply environment
Champion continuous improvement initiatives within manufacturing operations to enhance efficiency, quality, and productivity.
Responsibilities
Champion the development of a high-performance culture through the implementation of the Manufacturing Operating System (MOS) and continuous improvement methodologies.
Monitor and analyze plant key performance indicators (KPIs) at daily, weekly, and monthly intervals. Identify performance gaps and lead initiatives to eliminate losses and drive efficiency.
Empower and develop shop floor teams through training, coaching, and mentoring. Build internal capabilities in problem-solving, lean tools, and improvement methodologies.
Lead cross-functional improvement projects focused on reducing waste, improving productivity, and enhancing quality (e.g., SMED, material loss reduction, Kaizen events).
Drive the adoption of digital tools and systems (e.g., MES, Digital MOS) to support the journey toward a smart, data-driven factory.
Lead quality assurance and operational management for Pfizer contractors worldwide, ensuring product quality and regulatory compliance.
Compensation
The annual base salary for this position ranges from $176,600.00 to $294,300.00.* In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program.
Responsibilities
Provide Quality Leadership to support virtual site operating teams
Lead development, implementation and support of Quality Assurance/Quality Control systems
Partner with colleagues to develop and negotiate Quality Agreements
Partner with Global Logistics and Network Services to ensure GDP oversight
Drive continuous improvement of Pfizer products, processes and quality systems
Requirements
Bachelor's degree in Pharmacy, Engineering or related science
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.
Locations (2)
Horsham, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
The anticipated base pay range for this position is : $94,000.00 - $151,800.00
Responsibilities
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
E2E Supply Planner
6084-Janssen Research & Development Legal Entity · Posted Nov 5, 2026
The E2E Supply Planner is responsible for planning and managing the day-to-day activities of the Clinical Supplies department such as packaging, labeling, assembling and shipping of clinical supplies used in clinical trials.
Locations (2)
Beerse, Antwerp, Belgium
United States
Compensation
The anticipated base pay range for this position is: €61,200.00 - €98,210.00
Responsibilities
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.
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
Requirements
Bachelor’s Degree in business or science
Nice to have: Insight into a clinical supply environment in a pharmaceutical industry
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
RAŽOŠANAS NODAĻAS VADĪTĀJS/-ACV-Online Recruitment · Mārupe, Latvija
EngineerTenneco · Changzhou, China