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Wireless Cellular Standards Engineer

Apple, Inc.

•

No location provided

Full-time

At Apple, we work every single day to craft products that enrich people's lives. Do you love working on challenges that no one has solved yet? As a member of our cellular standards group, you will have the unique and rewarding opportunity to shape the global wireless industry and contribute to upcoming products that will delight and encourage millions of Apple's customers every single day! In this technical role, you will be at the center of our cellular standards group responsible for promoting
Posted 60+ days ago | Updated 1 day ago

Engineering Technician

Flextronics

•

Buffalo Grove, Illinois, USA

Full-time

Job Posting Start Date 07-09-2025 Job Posting End Date 08-09-2025 Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraord
Posted 23 days ago | Updated 6 hours ago

Manufacturing Coordinator - SAP

Select Source International

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Madison, Wisconsin, USA

Contract

Manufacturing Coordinator 6+ months extendable contract Description: The Manufacturing Coordinator position is responsible for supporting daily production operations. This position is responsible for issuing and tracking production orders, coordinating material and resource needs, maintaining accurate documentation, and facilitating communication between cross-functional teams to ensure smooth workflow and on-time delivery of products. This role assists the Production Leadership team and coor
Easy Apply
Posted 15 days ago | Updated 20 hours ago

Engineer III, Systems Engineer

Katalyst Healthcares and Lifesciences

•

San Diego, California, USA

Full-time

Responsibilities: Verification & validation Engineer will have the following responsibilities: A strong technical background and experience g in the medical device industry (Translation of User/Business Needs to System Requirements, Requirements Management, System Architectural Development, Functional Modeling, Systems Integration, Statistical Test Design, Verification and Validation, Hazards Analysis, and Failure Modes Effects Analysis), and/or other engineering disciplines within the medical
Posted 32 days ago | Updated 6 hours ago

Technical Training Program Specialist

B. BRAUN MEDICAL (US) INC

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Irvine, California, USA

Full-time

B. Braun Medical, Inc. Company: B. BRAUN MEDICAL (US) INC Job Posting Location: Irvine, California, United States Functional Area: Human Resources Working Model: Onsite Days of Work: Thursday, Wednesday, Tuesday, Friday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 4306 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nut
Posted 3 days ago | Updated 17 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

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Princeton, New Jersey, USA

Full-time

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases.
Posted 24 days ago | Updated 6 hours ago

Clinical SAS Programmer

Katalyst Healthcares and Lifesciences

•

Minneapolis, Minnesota, USA

Full-time

Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables, figures, and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements. Provides input in the design and development of case report forms and clinical databases.
Posted 12 days ago | Updated 6 hours ago

Quality Assurance Specialist-Core Laboratory

Johns Hopkins Medicine

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Baltimore, Maryland, USA

Full-time

The Johns Hopkins Hospital is a world-renowned leader in patient care, serving the greater Baltimore community and patients from all across the globe. Our friendly and knowledgeable staff teams provide support throughout our many specialty departments and centers, from primary visits to emergency care. What Awaits You? Career growth and development Tuition Assistance Diverse and collaborative working environment Affordable and comprehensive benefits package Location: Johns Hopkins Hospital, B
Posted 23 hours ago

Wireless Cellular Standards Engineer

Apple, Inc.

•

No location provided

Full-time

At Apple, we work every single day to craft products that enrich people's lives. Do you love working on challenges that no one has solved yet? As a member of our cellular standards group, you will have the unique and rewarding opportunity to shape the global wireless industry and contribute to upcoming products that will delight and encourage millions of Apple's customers every single day! In this technical role, you will be at the center of our cellular standards group responsible for promoting
Posted 60+ days ago | Updated 5 hours ago

Controls Validation Engineer

BEPC, Inc.

•

Irvine, California, USA

Contract

Summary Join our team as an Electrical/Controls Engineer specializing in IT and equipment validation for cutting-edge medical device manufacturing. In this role, you will support Lifesciences Plant Operations Engineering by leading and executing validations for PLCs, SCADA systems, and other manufacturing equipment. You ll work cross-functionally with engineering, quality, validation, and regulatory teams to ensure compliance with FDA, ISO 13485, and 21 CFR Part 11 standards. This position blen
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Posted 1 day ago

Manufacturing Supervisor - 3rd Shift

BAXTER

•

Round Lake, Illinois, USA

Full-time

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform h
Posted 1 day ago | Updated moments ago

Manufacturing Supervisor - 3rd Shift

BAXTER

•

Island Lake, Illinois, USA

Full-time

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform h
Posted 1 day ago | Updated moments ago

Manufacturing Supervisor - 3rd Shift

BAXTER

•

Harvard, Illinois, USA

Full-time

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform h
Posted 1 day ago | Updated moments ago

Manufacturing Supervisor - 3rd Shift

BAXTER

•

Salem Lakes, Wisconsin, USA

Full-time

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform h
Posted 1 day ago | Updated moments ago

Manufacturing Supervisor - 3rd Shift

BAXTER

•

Northbrook, Illinois, USA

Full-time

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform h
Posted 1 day ago | Updated moments ago

Sanitation Manager

Saicon Consultants Inc.

•

Toledo, Ohio, USA

Full-time

Job Title: Sanitation Manager Location: Toledo, OH 43613 Position Type: Full-Time / Permanent Shift: 3rd Shift Industry: Food Manufacturing Facility Type: Unionized About the Role: One of our clients is seeking a strong, hands-on Sanitation Manager to lead and elevate sanitation efforts in their food manufacturing facility in Toledo, OH. The ideal candidate brings CIP expertise, food safety knowledge, and people-first leadership, with a strong track record of training, coaching, and change mana
Easy Apply
Posted 22 days ago | Updated 4 days ago

Engineer Disposables and Sustaining

Katalyst Healthcares and Lifesciences

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Plymouth, Minnesota, USA

Full-time

Responsibilities: Create new 3rd party supplier documentation including design specifications, labelling, design drawings, etc. for peritoneal dialysis disposable sets. Create, modify, and maintain design history files. Perform change control assessments. Work closely with project manager and technical lead to achieve project commitments. Adhere to design control procedures, general safety rules, company policies and procedures, FDA and international regulations and guidance. Requirements:
Posted 18 days ago | Updated 6 hours ago

Software Engineer - Embedded C, C#, C++ | Marlborough, MA

Michael Page International

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Marlborough, Massachusetts, USA

Full-time

Join a revolutionary medical device manufacturing organizationWork with a team making a difference to patients all over the world About Our Client The company is a medical device organization that design and develop cutting-edge software for complex medical devices. They have an FDA approved device that is live in the US, Europe & Asia and they're looking to further grow their R&D team with this hire, and plan to continue their growth for the remainder of 2025 and into 2026! Job Description
Posted 15 days ago | Updated 2 hours ago

MES Engineer with Werum PAS-X

PDDN Inc

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New York, New York, USA

Contract, Third Party

Role: MES Engineer Location: New York, NY / Raritan, NJ Interview: Phone/Skype Job Type: Contract JOB DESCRIPTION: PAS-X Senior Engineer Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes. Key Responsibilities: Development\Modification\Upgrade\Enhancement of MBR s and GMBR
Easy Apply
Posted 11 days ago | Updated moments ago

Validation Engineer

Katalyst Healthcares and Lifesciences

•

North Haven, Connecticut, USA

Full-time

Responsibilities: As a Validation Engineer within the Mold & Capital Tooling Organization, you'll play a pivotal role on a global enterprise team, collaborating with various sites around the world. In this role, you'll facilitate or perform critical validation & qualification activities, ensuring the seamless release of high-quality injection molded components that drive our mission forward. Ensure proper qualification and validation of suppliers and their processes, ensuring supplier meets th
Posted 7 days ago | Updated 6 hours ago