101 - 120 of 511 Jobs

Microbiology Team Lead

ITS Technologies, Inc.

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

JDE Developer

VC5 Consulting

Bolingbrook, Illinois, USA

Contract

JDE Developer Contract-to-Hire Hybrid (Bolingbrook, IL) We are seeking a skilled JD Edwards Developer to join a high-impact internal applications team supporting a leading engineer-to-order manufacturer. This is a hybrid contract-to-hire role where youll work closely with business and IT leadership to modernize, integrate, and optimize the JDE EnterpriseOne 9.2 environment. Youll translate business requirements into actionable solutions, lead development efforts, and bring your expertise in Or

Automation Controls Engineer (2ndShift)

Bytecubit Technologies

Indianapolis, Indiana, USA

Contract

Job Title: Automation Controls Engineer (2nd Shift)Location: Indianapolis, INDuration: 6 monthsPay Rate: $45/hr-$55/hr (depending on experience) Job Description: This role will be responsible for supporting the design, installation, and validation for the sterile purification and recycling isolators into commercial production. Bachelor s degree in engineering, Computer Science, Automation, or related field with 7+ years of relevant engineering experience in the Pharmaceutical or Chemical indust

AME Automation Engineer

GE Healthcare

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

Clinical Data manager

Intone Networks Inc.

Remote

Contract, Third Party

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

Validation Engineer

Abbott Laboratories

Columbus, Ohio, USA

Full-time

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ABOUT ABBOTT Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future

Process Engineer

Merck KgaA

Indianapolis, Indiana, USA

Full-time

Work Location: Indianapolis, Indiana Shift: No Department: LS-SC-POEMA Clinical Tech Services Recruiter: Katherine Hall Hiring Manager: Stan Le This information is for internals only. Please do not share outside of the organization. Your Role: Provide key engineering support and project coordination for all phases of plant operations, including interfacing with internal and external clients for product technology transfers and manufacturing. Offer technical support for processes and product in

Project Manager

Beacon Systems, Inc

Lansing, Michigan, USA

Third Party, Contract

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. Position: Project Manager Location: Onsite - Lansing, MI Duration: Long term Key Responsibilit

Clinical SAS programmer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, 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. Perf

SAP LSP Consultant - Indianapolis, IN (Onsite) - AK

ASCII Group LLC

Indianapolis, Indiana, USA

Contract, Third Party

The following requirement is open with our client. Title : SAP LSP Consultant Location : Indianapolis, IN (Onsite) Relevant Experience (in Yrs.) : 6+ Detailed Job Description: SAP S/4 HANA Implementation & Support: Lead or support end-to-end implementation of SAP S/4 HANA solutions with a special focus on Logistics Execution and Supply Chain Management (SCM) modules, particularly Logistics Service Provider (LSP) functionalities.3PL Integration: Design, configure, and optimize S/4 HANA processes

Validation Specialist CSV & OT Systems

Galent

Muskegon, Michigan, USA

Contract, Third Party

We are seeking a skilled Validation Specialist with hands-on experience in Computer System Validation (CSV) and Operational Technology (OT) systems. The successful candidate will support validation activities across control systems such as DeltaV, ABB DCS, Historian, MES, and other regulated automation platforms. You will work under the direction of the Validation Lead, Automation Lead, and Project Manager, performing validation tasks and ensuring compliance with GxP, FDA, and cGMP guidelines. K

CQV Engineer

Katalyst Healthcares and Lifesciences

Brooklyn, New York, USA

Full-time

Responsibilities: Develop commissioning and qualification protocols for HVAC, purified water systems, clean utilities, and other critical utilities according to regulatory requirements (GMP, FDA, etc.). Execute commissioning and qualification activities for utilities systems, ensuring adherence to project schedules and quality standards. Conduct risk assessments, impact assessments, and gap analyses related to utilities systems. Coordinate with cross-functional teams including engineering, q

Adobe Campaign Technical Lead/Architect

Codinix Technologies Inc.

New York, New York, USA

Contract

Job Description We are seeking an experienced and strategic Adobe Campaign Technical Lead / Architect to lead our marketing technology initiatives. The ideal candidate will possess a deep understanding of Adobe Campaign platforms and related Adobe Experience Cloud tools, with a strong track record of designing and implementing scalable, data-driven marketing solutions. This role requires both hands-on technical skills and leadership capabilities to drive innovation and campaign effectiveness. Wo

Embedded Tester (SIT)

My IT LLC

Alameda, California, USA

Full-time, Contract

Job Title: Embedded Tester (SIT) Location: Alameda, CA (Local candidates only) Contract:6+months Exp. Level: 8-12 years Job Summary: We are seeking a highly skilled and detail-oriented Software Integration Tester (SIT) to join our team in Alameda, CA. This role is focused exclusively on device-level testing for a highly safety-critical handheld medical device. The ideal candidate will have a strong background in embedded systems, particularly in C and C++, and experience working in both RTOS and

Controls Engineer III

Thermo Fisher Scientific

Logan, Utah, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Discover Impactful Work: You will be part of the manufacturing engineering team to develop new manufacturing equipment that

Automation Control Engineer

Katalyst Healthcares and Lifesciences

South Plainfield, New Jersey, USA

Full-time

Responsibilities: Support design reviews, debugging, acceptance, and validation of equipment developed by external suppliers. Assist in decommissioning and recommissioning of equipment to ensure proper functionality and compliance. Conduct and analyze Gauge Repeatability & Reproducibility (GR&R) studies and Process Capability assessments. Work with automation control systems, including PLCs, HMIs, Vision Systems, Servos, and Robots. Develop and optimize programs for Allen-Bradley/Rockwell Automa

Senior Software Quality Engineer, Post Market

Stryker

San Jose, California, USA

Full-time

Work Flexibility: Hybrid Stryker is hiring a Senior Software Quality Engineer, Post Market to support our Medical's Digital Health division and portfolio Software as a Medical Device (SaMD)/Software in a Medical Device (SiMD) and Software as a non-medical device (SaND) to support projects as a quality engineer for post-market activities to drive customer quality. Workplace Flexibility & Location: This hybrid role requires candidates to be within commuting distance of one of the following locat

Identity Data Protection Engineer

Talent Groups

Remote

Contract

Position: Identity Data Protection Engineer Location: Remote Job Type: Contract Duration: 12 months to start Job Description: This person will be responsible for the day-to-day administration of the data classification and protection systems. This person will consult with members of the technical and business communities to identify and label data. S/he will analyze and resolve complex software and hardware problems and ensure that the correct processes are followed in change management for t

Senior Consultant Veeva R&D Products

Nityo Infotech Corporation

Bridgewater, New Jersey, USA

Full-time

Job Role: Senior Consultant Veeva R&D Products Job location: Bridgewater NJ Job Type: Full Time Job Description: Client is seeking Life science Consultant with proven requirement gathering skills and have experience in preparing technical requirement documents based on the information gathered in technical workshops. Required Qualifications: Candidates need to be in and around or willing to relocate to Bridgewater NJ and work from our infosys office.Bachelor s degree or foreign equivalent re

Principal Validation Engineer

Johnson & Johnson

Danvers, Massachusetts, USA

Full-time

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m