fdma jobs

Forest, Mississippi

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10d ago

About Beacon Systems, Inc Beacon Systems, Inc, delivers Program Management, Science, Engineering, and Technology Solutions to Federal, Commercial, State, and Local Agencies. We are a subsidiary of Radiant Digital Solutions. Our Technology support to many DoD Agencies, NASA, Voice of America, FDA, and State Agencies such as State of FL, RI, MS, ND, VA, and WV extends our delivery of solutions worldwide. Job Title: Senior Natural Developer Location: On-site - Jackson, MS Contract Duration:3 Years

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Contract, Third Party

Depends on Experience

Project Manager – Medical Devices (Operations / Manufacturing / Supply Chain)

Santa Rosa, California

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Yesterday

Project Manager Medical Devices (Operations / Manufacturing / Supply Chain)Location: Santa Rosa, CA Onsite Minneapolis, MN Onsite Duration: ContractExperience: 5+ Years (US Project Management experience required) Job DescriptionWe are seeking an experienced Project Manager with a strong background in the medical device industry to support cross-functional initiatives across Operations, Manufacturing, and Supply Chain. The ideal candidate will have hands-on experience working in FDA-regulated

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Contract

Depends on Experience

Sr Process Engineer/Project Manager (Pharma/cGMP/FDA)

Philadelphia, Pennsylvania

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Today

Sr Process Engineer/Project Manager (Pharma/cGMP/FDA) - Remote (East Coast) This Jobot Job is hosted by: Tony Barhoum Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $115,000 - $150,000 per year A bit about us: Full-Service Engineering Consulting Firm with a broad range of projects and clients within the private and public marketplaces. Our design engineers provide cost-conscious, reliable, Design/Build Solutions to meet our Client's needs.

Full-time

USD 115,000.00 - 150,000.00 per year

CSV Engineer

Hybrid in Raritan, New Jersey

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21d ago

Job Description: Experience in validating ERP/SAP/ MES Manufacturing applications 3+ years experience with System Development Lifecyle 7+ years experience in Computer System Validation (Based on the role selected) Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation Experience in writing and executing docum

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Contract

Depends on Experience

Sr. CSV Engineer

Oregon City, California

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Today

Summary : Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies. Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems Create and modify validation documentation including but

Full-time

Clinical SAS Programmer

Edison, New Jersey

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Today

Responsibilities: Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to ensure high-quality within timeline and budget. Conduct hands-on validation/QC of CRO deliverables to ensure high-quality (SDTMs, ADaMs, TFLs) and ensure accuracy of clinical trial results for internal and external audiences. Ensure all relevant deliverables including investigator brochures, publications, all regulatory submissions (

Full-time

Staff Engineer, Process Development

Warwick, Rhode Island

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Today

Job Description Summary Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human e

Full-time

Principal Engineer, System

San Jose, California

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Today

Please Note: To provide the best candidate experience amidst our high application volumes, each candidate is limited to 10 applications across all open jobs within a 6-month period. Advancing the World's Technology Together Our technology solutions power the tools you use every day--including smartphones, electric vehicles, hyperscale data centers, IoT devices, and so much more. Here, you'll have an opportunity to be part of a global leader whose innovative designs are pushing the boundaries o

Full-time

USD 214,060.00 - 341,940.00 per year

Engineering Project Manager

Skaneateles, New York

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Today

Job Description: Lead cross-functional teams in complex engineering assignments, ensuring compliance with medical device regulations and effective project execution. This role requires a strong focus on project management, collaboration, and problem-solving across traditional product lines. Responsibilities: Independently plan, execute, and direct cross-functional engineering projects, adapting standard engineering principles to develop innovative solutions. Manage projects consisting of cross-

Full-time

Sr. Validation Engineer

Wilson, North Carolina

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Today

Summary: The Senior Validation Engineer will lead and execute commissioning and qualification (C&Q) activities for automation systems at the. This role ensures compliance with GMP regulations and internal quality standards, supporting the successful delivery of validation documentation and execution for new and existing systems. Roles & Responsibilities: Lead and manage C&Q lifecycle activities including URS, DQ, IQ, OQ, and PQ for automation and process systems. Collaborate with cross-function

Full-time

CSV Engineer

Bothell, Washington

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Today

Summary: Responsible for preparing and executing test documentation for GMP computerized systems as well as providing support in the troubleshooting of issues during test execution. You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies. Coordinate with multi-disciplinary validation team and be responsible for the validation of automated equipment and control systems Create and modify validation documentation including but

Full-time

Controls Engineer

North Haven, Connecticut

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7d ago

Role Summary: This position supports high-precision automated manufacturing lines for Class II/ medical devices. The role requires deep expertise in controls engineering, Rockwell automation platforms, and validation of regulated systems. The engineer will design, program, troubleshoot, and optimize controls architectures that drive equipment reliability, throughput, and compliance. Key Responsibilities: Develop, modify, and optimize Rockwell Automation (Allen-Bradley) PLC and Motion Control pr

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Contract

Depends on Experience

Senior Controls Engineer Medical Devices

North Haven, Connecticut

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Today

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Contract

Senior Embedded Software Engineer

Hybrid in Schaumburg, Illinois

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Today

Position Description ISCO is looking for a Senior Embedded Software Engineer to help architect, develop and implement ISCO's new telecommunications products. This role has a wide scope that may include implementation of DSP algorithms, development of drivers and APIs, design of O&M functions, and even support of automated test development efforts. This role requires a Senior level Software Engineer with a broad range of skills, innovative spirit, and desire to work in a fast-paced, entrepreneur

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Full-time

depends on experience

Hardware Application Engineer

Santa Clara, California

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Today

NVIDIA Application Engineering is a department to provide technical support to NVIDIA global customers. Our main mission is delivering NVIDIA GPU and SoC related technical information to our customers, training our customers to design NVIDIA related products, collaborate with OEM/ODM for new feature development, and supporting our customers to efficiently build NVIDIA GPU and SoC related products into the market. We are now looking for a Hardware Application Engineer in Santa Clara with the abi

Full-time

USD 136,000.00 per year

Software Engineer C++

Tewksbury, Massachusetts

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Today

Leidos is looking for a talented Software Engineer to support new product development at Security Enterprise Solutions. As a Software Engineer on our diverse and collaborative team, you will work alongside our expert Scientists and Engineers who belong to cross functional discipline, contributing to Leidos products with global impact on aviation security screening. You'll be honing your engineering skills with instrumentation domain products, real-time programming, and object-oriented design, a

Full-time

USD 87,100.00 - 157,450.00 per year

Manufacturing Electrical Engineer

Milpitas, California

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Yesterday

Job description: Manufacturing Electrical Engineer (Senior Level 7+ Years)Job Summary We are seeking a Senior Manufacturing Electrical Engineer with strong experience in medical device manufacturing and mandatory experience with the Electronic Communications Privacy Act (ECPA). This role supports electrical assembly, testing, supplier management, and product end-of-life activities while ensuring compliance with regulatory, quality, and privacy standards. The engineer will work cross-functionally

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Full-time

$40 - $45

Validation Engineer II

Greenville, North Carolina

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Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single

Full-time

Regulatory Affairs Specialist (Small Molecule IND, NDA, Module 3)

Santa Clarita, California

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6d ago

Regulatory Affairs Specialist (Small Molecule IND, NDA, Module 3) Job Summary This critical role demands extensive hands-on expertise in modifying regulatory strategies, authoring scientifically robust Chemistry, Manufacturing, and Controls (CMC) documentation within Module 3 of the eCTD, and managing submissions for Investigational New Drug (IND) and New Drug Applications (NDA) specifically for small molecule drugs. Key Responsibilities Submission Authoring & Management: Lead the planning,

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Contract

$100

Wireless Systems Engineer (Hardware)

Seattle, Washington

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Today

This Jobot Job is hosted by: Christina Finster Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $130,000 - $200,000 per year A bit about us: Our client was founded with the intention of delivering on the promise of what Internet-of-Things (IoT) was supposed to be. They're building a global Bluetooth network dedicated to machine-to-machine connectivity. Our client is an early-stage, venture-backed startup supported by some of the best investor

Full-time

USD 130,000.00 - 200,000.00 per year

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