1,000+ matching jobs for “Material Program Manager”

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Rockwell Automation

MATERIAL HANDLER - 4

Cambridge, Ontario, Canada

Full time

Pay posted by employer$56,400–$70,500

As a Material Handler 4, you will support the flow of materials throughout the facility by receiving, storing, picking, …

Added Oct 29, 2026

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RTX

Program Operations Manager (Onsite)

Largo, Florida, United States

… market. Join us and help shape the future of aerospace and defense. This position will directly support a Program Management Office (PMO) in leading manufacturing strategy for programs in development. This role is …

Added Oct 27, 2026

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Conagra Brands

Associate Material Planner

Archbold, Ohio

Full time

Pay posted by employer$59,000–$79,000

… the handoff window and ensure constraints are visible to centralized planning teams. Translate approved Material Resource Planning and supply plans into daily and weekly call-off and delivery schedules for raw and …

Added Nov 3, 2026

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Conagra Brands

Material Operations Specialist

Omaha, Nebraska, United States

Full time

Pay posted by employer$64,000–$95,000

… and translate raw and pack (R&P) needs across execution and operational horizons to ensure uninterrupted material availability at supply points. • Execute automated MRP runs, analyze outputs, and manage Purchase …

Added Nov 3, 2026

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Conagra Brands

Material Operations Specialist

Omaha, Nebraska, United States

Hybrid
Full time

Pay posted by employer$64,000–$95,000

Added Nov 3, 2026

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KLA

Staff Material Scientist

Singapore, Singapore

Full time
Regular

… developed. The Office of the CTO also provides technical input into KLA’s strategic planning process, program reviews and Product Life Cycle (PLC) phases. We provide our broad technology expertise and cross-division …

Added Oct 15, 2026

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Design & Material Intern

EMEA > CHE > Stabio > Stabio - VF Campus VF1

… and support the creation of future-focused product. In this role, you will work alongside Designers and the Material specialist to explore new concepts, explore materials and trims and elevate existing product ranges. The …

Added Oct 27, 2026

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Northern Trust

AI Program Manager (Product Development)

Chicago, Illinois, United States

Regular

Pay posted by employer$114,700–$194,900 USD

… clear oversight of outcomes, dependencies, risks, resources, costs and decisions. This is a generalist Program Manager position. The successful candidate may subsequently lead other strategic, regulatory, product, …

Added Oct 16, 2026

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Northern Trust

AI Program Manager (Product Development)

London, England, United Kingdom

Regular

Added Oct 16, 2026

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Northern Trust

AI Program Manager (Product Development)

Limerick, Munster, Ireland

Regular

Added Oct 16, 2026

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RTX

Manager, Program Management - ISS (Onsite)

US-CT-WINDSOR LOCKS-B1A ~ 1 Hamilton Rd ~ BLDG 1A

… U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.

 Security Clearance Type: None/Not Required

 Security Clearance Status: Not …

Added Oct 30, 2026

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Intel

Supply Chain Program Manager (Contract)

Albuquerque, New Mexico, United States +2 locations

Pay posted by employer$52,000–$200,000 per year

… on the planet. Life at Intel: https://jobs.intel.com/en/life-at-intel The Role and Impact As a Supply Chain Program Manager, you will play a pivotal role in orchestrating the seamless flow of materials to support New …

Added Oct 27, 2026

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GE Vernova

Sr Manufacturing Manager 3 - Uranium Material Accounting & Management

Wilmington NC USA

Pay posted by employer$104,600–$174,400 USD

… accounting, and compliance for our nuclear fuel operations. In this role, you will develop integrated material plans, maintain rigorous book-to-physical inventory controls, and ensure full compliance with NRC and …

Added Oct 30, 2026

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IQVIA Holdings

Program Delivery Manager IP Administration

Durham, North Carolina, United States

Pay posted by employer$68,400–$171,000

… ancillary supply related questions in close collaboration with the Ancillary Support Associate (ASA)/ Site Manager (SM). Develop IP administration training materials. Set up and attend mock runs on IPPI administration …

Added Oct 15, 2026

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Stanley Black & Decker

Program Manager (m/w/d)

Rheingau-Taunus-Kreis, Idstein, Deutschland

Full time
Regular

Position: Program Manager (M/W/D) Standort: Idstein Arbeitsmodell: hybrid (2 Tage onsite / 3 Tage remote) Beschäftigung: …

Added Oct 27, 2026

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Rockwell Automation

MATERIAL HANDLER - Level 2

Cambridge, Ontario, Canada

Full time

Pay posted by employer$43,200–$54,000

As a Material Handler Level 2, you will support manufacturing and distribution operations by receiving, storing, picking, …

Added Oct 27, 2026

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Caterpillar

Technology Program Manager-Business Operations

Irving, Texas, United States

Pay posted by employer$128,470–$192,710

… era of construction autonomy at Caterpillar. Job Summary: Cat Technology is seeking a Lead Digital Project Manager to lead portfolio operations, financial planning, workforce coordination, and business execution for a …

Added Oct 27, 2026

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IQVIA Holdings

Gestionnaire de programme / Program Manager

Mississauga, Canada

Pay posted by employer$64,100–$106,900

… manière constructive et à adapter son approche de leadership en conséquence. Job Overview Responsible for program management including set up, implementation, and monitoring of client-specific patient support programs. …

Added Oct 15, 2026

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Conagra Brands

Production and Material Planner

Henning, Illinois

Full time

Pay posted by employer$64,000–$95,000

Develop and manage production and material plans, including detailed schedules, sequencing, and escalation of short-term material issues to align with …

Added Nov 3, 2026

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Applied Materials

System Project Manager, Non-Technical Program Manager

Kalispell, Montana, United States +1 location

Pay posted by employer$68,000–$93,500

Support specific project and program objectives as defined in the areas of responsibility, and that necessary preliminary activities (e.g., …

Added Oct 27, 2026

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IQVIA Holdings

Program Delivery Manager IP Administration

Durham, North Carolina, United States

Pay posted by employer$68,400–$171,000

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About this opportunity

Original employer description

External Job Description

Overview:

The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and procedure of the IPPI (Investigational Product Preparation and Administration Instructions), specific to drug administration in the area of clinical research. The SIPS will play a lead role in the development of safe, efficient, and effective IP administration in clinical trials. The SIPS will be the key internal and external interface to ensure overall IPPI ad ministration adherence. The SIPS will be co-author of the IPPI, and will be responsible for training slide development, training level assessment evaluation, and internal staff training. The SIPS will give input in ancillary supply selection and ancillary supply related questions, study feasibility, site assessment and mentoring for IPPI. He/she will contribute to continuous IPPI process improvement. The SIPS will mainly focus on SIPS tasks for trials with an IPPI.

Deliverables:

Services rendered will adhere to applicable Johnson & Johnson SOPs, Wis, policies, local regulatory requirements, etc.
Co-author of the IPPI and review/provide input on all specific forms related to IP administration and dosing for all types of trials with an IPPI such as:
- Administration routes (IV/SC/IM/intravesical/intraperitoneal/blood and cell products, etc.)
- IV access devices (central vs peripheral, Hickman, PICC, Port, PIV, midline, etc.)
- Priming and flushing procedures
- Filters
- Hygienic standards
- Medical devices (IV pumps, syringe pumps, plasma therm, etc.)
Support IPPI related initiatives and working groups. Actively participate in IPPI and all other nursing practice and scientific discussions. Track and integrate evolving trends in nursing practice into current and future IPPIs.
Provide input in ancillary supply selection, Ancillary Supply Questionnaire and coordinate ancillary supply related questions in close collaboration with the Ancillary Support Associate (ASA)/ Site Manager (SM).
Develop IP administration training materials.
Set up and attend mock runs on IPPI administration before first formal IP administration at the investigational site if deemed necessary.
Support SM/IDM with resolving site IPPI related issues and site training (if applicable) according to local guidelines and blinding requirements.
Assist in site assessments/pre-trial assessment activities and study feasibility, providing
recommendation from local area about site/investigator selection in collaboration with the trial team and develop IP related questions for site feasibility questionnaire.
Attend site initiation visit to support SM if deemed necessary.
Responsible for internal team training of administration process for all versions of the IPPI according to internal Standard Operating Procedures (SOPs)/Work Instructions (Wls)/Instructions for Use (IFUs) and policies for internal staff.
Point of contact for the internal study team (LTM/SM/IDM) for questions and issue resolution related to the IP administration.
Conduct ongoing dialogue with customers to understand site perspectives and enhance educational efforts as it relates to study drug administration.
Present data and information in a manner appropriate to the audience, identifying groups that would benefit from presentations and information.
Perform all administrative requirements in a timely, accurate and compliant manner (e.g. expense reports, documentation of activities, vTMF filing, CTMS).

Metrics/KPIs:

Metrics/KPIs governing these services are outlined in the QOP document.

Interfaces - Primary/Other:

Primary interfaces: Provider Functional Manager, Global Trial Leader, Country Trial Manager, Local Trial Manager, Site Manager, Pharmacy Investigational Product Specialist, Site Investigational Product Specialist, Ancillary Support Associate, Independent Drug Monitor Manager, Independ ent Drug Monitor, DPDS-team, Clinical Supply Integrator, CMC Leader, Study Responsible Physician, Study Responsible Scientist, Global Clinical Research Associate, CTL&D Specialist
Other Interfaces: Quality and Compliance Manager/Specialist, R&D/Local Operating Company staff (including Medical Affairs), Bioresearch Quality and Compliance (BRQC), Investigators and their delegates at site (trial site personnel).

Education and Experience Requirements:

A degree in general nursing is required.
3- 4 years of recent clinical/hospital experience is required; however, other relevant experience may be considered by the hiring manager when considering the candidate's eligibility.
Experience in antibody treatment, (Oncology (hematology and solid tumor) and / or Immunology
Therapeutic Area
Clinical trial research experience.
Knowledge of the drug development process and on International Council on Harmonization (ICH)/Good Clinical Practices (GCP) is an asset.
Strong leadership, process initiative, influencing and mentoring skills.
Experience working with virtual meeting software, Microsoft suite, including word, power point and excel and clinical systems.
Innovative and creative mindset with strong attention to details.
Strong written, oral, and interpersonal communication skills.
The ability to multi-task, work on multiple trials in parallel in different disease areas.
The ability to collaborate with all levels of management across a matrix organization.
Problem solving skills with ability to make decisions. to manage difficult clinical scenarios
Must be proficient in speaking and writing in the country language and English.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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