FDA Jobs

121 - 140 of 479 Jobs

Labelling ManagerJob Title - Labelling Manager

AltezzasysCompany Name - Altezzasys

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Irving, Texas, USA

Contract, Third Party

Job Title:- Labelling Manager Location:- Irving, Texas (Onsite) Contract Job Description:- Lead and Coordinate Labeling Design Change projects for US and Global Medical device products. Ensures all Design change activities are planned, approved, and executed. Coordinate various team member activities to ensure project plan targets are defined and met.Prepare and executes a Design Change Notice to describe the proposed change, the project plan for accomplishing the design changes, and Design tran

Sr. SAS ProgrammerJob Title - Sr. SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Durham, North Carolina, USA

Full-time

Responsibilities: The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies. In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members. Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment. Serves as lead programmer for assigned projects to provide statistical and programming support i

Associate EngineerJob Title - Associate Engineer

ACL DigitalCompany Name - ACL Digital

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New Albany, Ohio, USA

Full-time

Fully onsite at New Albany OH Day shift - 6:30am - 3pm (Shift times may vary) **Manager is open market rate candidate Ideal Candidate: Looking for someone with some schooling and some maintenance experience or someone with no schooling and strong experience. Please read top 3 skillsets. Associate Technical Engineer - Equipment Maintenance: Let's do this. Let's change the world. In this role you will provide technical engineering support on all system/equipment optimization strategies, upgrades

Senior SAP MM/WM Functional Consultant (Master Data & Inventory)Job Title - Senior SAP MM/WM Functional Consultant (Master Data & Inventory)

RMSS INCCompany Name - RMSS INC

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Minneapolis, Minnesota, USA

Contract

Job Summary: We are seeking multiple (4-6) seasoned SAP MM/WM implementation specialist with deep domain expertise in master data governance and inventory management for manufacturing in the Medical Equipment / Healthcare industry . The consultant will be responsible for comprehensive SAP implementations focusing on material master data, inventory optimization, and warehouse management in regulated environments. Key Responsibilities: Lead the SAP MM/WM/EWM implementation projects from requiremen

Validation Engineer IIIJob Title - Validation Engineer III

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Mounds View, Minnesota, USA

Full-time

Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Perform, oversee, and guide supplier process validations (IQ/OQ/PQ) for sterile barrier packaging material manufacturing processes. Ensure supplier process validation requirements (CTQs, drawings, specifications, risk levels, and protocols) are communicated, understood, and executed. Collaborate with suppliers to review and approve validation documentation, including prot

Need Senior Manufacturing Quality EngineerJob Title - Need Senior Manufacturing Quality Engineer

Montek SystemCompany Name - Montek System

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Ayer, Massachusetts, USA

Contract, Third Party

Onsite, Devens location Work Schedule: Mon - Fri, First shift (8:30AM - 5PM) Top Skills/Must Haves: Quality Control Equipment experience preferredTechnical WriterInvestigations/Deviation experience preferred Job Description/ Responsibilities: Provides Quality Assurance (QA) support to Devens Site and reporting Manger through quality review andapproval of Investigations and Corrective Actions. Decision making of non-conformance through a deep understanding of Quality Systems Regulatory expectati

Business Development ManagerJob Title - Business Development Manager

Showman StaffingCompany Name - Showman Staffing

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Remote

Full-time

Job Title: Sr.Business Developer Manager Experience: 6+yrs Location: Remote-Travel required-100% client location-Candidates should be in USA Job: Permanent Full Time Requirement Role Overview We are seeking a passionate and driven Sales professional to accelerate our growth in the Healthcare and MedTech space one of the most rapidly evolving sectors today. You will work with a high performing team targeting innovative healthcare providers, MedTech firms, and digital health disruptors to bring c

Senior Business Developer ManagementJob Title - Senior Business Developer Management

Showman StaffingCompany Name - Showman Staffing

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Remote

Full-time

Business developer ManagerJob Title - Business developer Manager

Showman StaffingCompany Name - Showman Staffing

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Remote

Full-time

Kubernetes Engineer - GPU Platform EngineeringJob Title - Kubernetes Engineer - GPU Platform Engineering

Beacon Systems, IncCompany Name - Beacon Systems, Inc

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Dallas, Texas, USA

Contract, Third Party

About Radiant Digital, IncRadiant Digital, Inc, delivers Program Management, Science, Engineering, and Technology Solutions to Federal, Commercial State, and Local Agencies. We are a subsidiary of Radiant Digital Services. We have a vast portfolio of clients across the country. 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. Position: Kubernetes Engineer - GPU P

Commissioning and Qualification EngineerJob Title - Commissioning and Qualification Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Raleigh, North Carolina, USA

Full-time

Responsibilities: Lead or support C&Q activities for pharmaceutical utilities and process equipment, ensuring compliance with industry standards and regulatory requirements. Execute FAT (Factory Acceptance Testing) to validate equipment functionality and performance. Support the qualification of Black and Clean utilities, such as water systems, clean steam, HVAC, and gas utilities. Perform process equipment qualification to meet GMP and production readiness standards. Develop and execute C&Q pro

Quality Assurance Associate Director, PharmacovigilanceJob Title - Quality Assurance Associate Director, Pharmacovigilance

Civica RxCompany Name - Civica Rx

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Petersburg, Virginia, USA

Full-time

Remote About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Tod

Quality Management Systems (QMS) Specialist (W2)Job Title - Quality Management Systems (QMS) Specialist (W2)

Sovereign TechnologiesCompany Name - Sovereign Technologies

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Irvine, California, USA

Contract

Title: Document Control Coordinator - QMS Location: Irvine, CA Onsite Document Control Specialist QMS Job Description We are seeking a dedicated Quality Management Systems (QMS) Specialist who will play a crucial role in ensuring compliance with internal and external regulatory requirements. This role involves engaging in the development of future state QMS for business needs, executing modifications, and contributing to the quality planning process. Responsibilities Ensure QMS compliance with a

Reliability EngineerJob Title - Reliability Engineer

Advantage TechnicalCompany Name - Advantage Technical

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Spencer, Indiana, USA

Full-time

Advantage Technical is hiring a Reliability Engineer in the Bloomington, IN area. Join a collaborative team focused on improving patient outcomes through data-driven investigations and continuous product improvement. Pay: $44.00/hour Qualifications: Bachelor's Degree (BS) in Engineering, Life Sciences, or related field with 2-4 years of relevant experience OR Master's Degree (MS) with 1-2 years of experience Experience working in FDA-regulated environments, preferably within medical devices or

Process EngineerJob Title - Process Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Morristown, New Jersey, USA

Full-time

Responsibilities: Support activities within MSAT-US, including the development of technical documentation, SOPs, and internal systems. Provide technical expertise in packaging and Pharma processes, equipment, materials, and component performance. Investigate and recommend new packaging technologies, systems, and materials for potential integration into Company packaging and Pharma manufacturing systems. Provide project management support for CMC and packaging projects related to late-stage N

Healthcare Data Scientist FHIR & HL7 ExpertiseJob Title - Healthcare Data Scientist FHIR & HL7 Expertise

E-Solutions, Inc.Company Name - E-Solutions, Inc.

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Philadelphia, Pennsylvania, USA

Third Party

Job title: - Healthcare Data Scientist FHIR & HL7 Expertise Location: Philadelphia PA Job Summary: We are seeking a curious and motivated Machine Learning Engineer to join the Foundational Data Analytics (FDA) Program - a strategic initiative aimed at building a modern, intelligent data ecosystem. In this role, you will support the development and deployment of machine learning models that power enterprise analytics, deliver predictive insights, and drive transformation across the healthcare

Microbiology Team LeadJob Title - Microbiology Team Lead

ITS Technologies, Inc.Company Name - ITS Technologies, Inc.

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Bowling Green, Ohio, USA

Full-time

Integrated Talent Strategies (ITS) is seeking a Microbiology Team Lead to work in the Perrysburg, OH area. This is a direct hire position that offers a variety of great benefits, including health insurance, 401(k), and paid time off.DescriptionResponsible for USP microbiological quality control testing on various products, including FDA-regulated OTC drugs, cosmetics, and EPA-registered disinfectants. Establishes microbial monitoring limits and oversees environmental monitoring to ensure facili

Sr MES PharmaSuite ConsultantJob Title - Sr MES PharmaSuite Consultant

SwanktekCompany Name - Swanktek

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Vacaville, California, USA

Contract

Client is seeking a highly experienced and resilient Senior Pharma Suite Owner's Representative to join our client's critical automation system replacement project in their state-of-the-art biopharmaceutical manufacturing facility. This individual will act as a key liaison, advocating for the client's best interests and ensuring the successful implementation of the Rockwell PharmaSuite MES. This is a demanding, long-term contract role requiring a professional who thrives in a high-pressure envir

Clinical Data managerJob Title - Clinical Data manager

Intone Networks Inc.Company Name - Intone Networks Inc.

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Remote

Third Party, Contract

Need stronger with working on Data Acquisition, DTAs and vendor relations. Responsibilities: Support the planning, setup, and acquisition of external clinical data at the study level, assisting in managing study start-up, conduct, and closeout activities.Assist in creating external data transfer agreements, ensuring alignment with Takeda Standards and specifications to support data integration, analysis, and reporting.Provide support in setting up infrastructure for external data to flow into T

AME Automation EngineerJob Title - AME Automation Engineer

GE HealthcareCompany Name - GE Healthcare

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Waukesha, Wisconsin, USA

Full-time

Job Description Summary We are seeking a detail-oriented and innovative Automation Engineer to join our Advanced Manufacturing Engineering (AME) team within a regulated medical device manufacturing environment. This role is responsible for designing, developing, and implementing automation solutions that enhance manufacturing efficiency, ensure product quality, and maintain compliance with FDA and ISO standards. The ideal candidate will have experience in highly regulated industries and a passio