121 - 131 of 131 Jobs

Principal Engineer

Aditi Consulting

New Albany, Ohio, USA

Contract

Payrate: $45.00 - $49.00/hr. Summary: Lead teams in the development of drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate will lead technical teams to ensure successful device development of these mechanical and electro-mechanical medical devices. The Principle Engineer will work closely with team members to develop detai

Senior Quality Engineer

Catapult Solutions Group

Chicopee, Massachusetts, USA

Full-time

Senior Quality EngineerQuality Engineering Department Location -Chicopee, MA - On-site position Role Type Full-time position About Our ClientOur client is an established manufacturing company specializing in sealed plastic film products for multiple industries, with a particular focus on medical device manufacturing. Operating in an ISO 13485 certified environment, they maintain the highest standards of quality and regulatory compliance. The company serves diverse markets requiring stringent qua

Project Manager

Stellar IT Solutions

Madison, Wisconsin, USA

Full-time, Part-time, Contract, Third Party

Job Title: Project Manager Sustaining Engineering & Fixture Development Location: Onsite Madison, WI Job Type: Full-Time / Contract Industry: Medical Devices / Engineering / Manufacturing Job Summary: We are seeking a skilled and detail-oriented Project Manager with a background in engineering to lead and manage multiple sustaining engineering and fixture development projects within a regulated medical device environment. This role will be based onsite in Madison, WI and will involve collabor

CQV Engineer-W2 ONLY

VetForce Solutions

Holly Springs, North Carolina, USA

Contract

Title: CQV Engineer Location: Holly Springs, NC-onsite Duration: 6-12+ Months CQV Engineer Responsibilities (Typical): * Upstream/downstream process and CQV support (ex. autoclaves, parts washers, incubators, Isolators, HVAC) * Managing and working collaboratively with clients quality representative to complete deviation investigation and resolution for problems and issues encountered during execution activities. Includes ability to complete root cause analysis * Supporting clients change manag

Manufacturing Engineer

Stellar IT Solutions

Madison, Wisconsin, USA

Full-time, Part-time, Contract, Third Party

Job Title: Manufacturing Engineer Location: Madison, WI Employment Type: [Contract] Reports To: Manufacturing Engineering / Facilities Manager Job Summary: We are seeking a detail-oriented and proactive Manufacturing Engineer to support and improve manufacturing processes, tooling, equipment, test systems, and documentation within a regulated medical device manufacturing environment. The Manufacturing Engineer will ensure compliance with quality systems and regulatory requirements, including

Industrial Engineer On W2 Only

Sovereign Technologies

Sumter, South Carolina, USA

Contract

Title : Industrial EngineerLocation : Sumter, SCDuration : 12 MonthsRate : $OpenVisa Status : Any work Status On W2 OnlyRelevant Experience: 8 Years Job DescriptionWe are seeking a detail-oriented and innovative Industrial Engineer to lead process optimization initiatives within our medical device manufacturing operations. This role is critical in ensuring that our production lines meet the highest standards of efficiency, quality, and regulatory compliance. The ideal candidate will bring a str

Sr. CSV Engineer

Net2Source Inc.

Muskegon, Michigan, USA

Contract

Join a Global Leader in Workforce Solutions - Net2Source Inc. Who We Are: Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 32 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision Right Talent. Right Time. Right Place. Right Price. Position: Sr. CSV Engineer Location: Muskegon, MI - onsite, 5 days a week

LIMS and QC Applications Consultant

Expedite Technology Solutions

Remote or Bridgewater, New Jersey, USA

Full-time, Contract

Solution Architecture and Design: Lead the design and development of LabVantage LIMS solutions tailored to business and laboratory needs. Develop system workflows, configurations, and integrations with other enterprise systems (e.g., S4 Hana ERP, MES, ELN, SDMS). Define data models, interface designs, and system configurations. Implementation and Deployment: Oversee installation, configuration, and validation of LabVantage LIMS applications. Develop and execute project plans, ensuring timely an

Veeva Admin/ Tech Lead

Atika Tech

No location provided

Contract

Position: Veeva Admin/ Tech Lead Location: Remote (Canada) Type: 6 months Contract to Hire Required Skills: Veeva Platform/UCV certified (Admin/Associate Admin) 10 + years of experience in Information Technology. 4+ years of experience in Pharma domain implementing/configuring Veeva Vault Must have an experience on Veeva CTMS, TMF, Site connect and SSU. Experience in end-to-end Veeva implementations as a Technical Lead Hands-on expertise in configuring Veeva. Extensive experience on Mile

Serialization Execution System

KK Associates

Indianapolis, Indiana, USA

Full-time, Contract, Third Party

Position:- :- Serialization Execution System (Validation) Location: - Indianapolis, IN JD:- SCADA, PLC, Systech, Serialization, Automation, Packaging line and vision systems Provide tier2 support to the Serialization Execution System. Assist existing teams in software qualification and validation activities and further assist the Serialization support team in managing serialized lines. Develop a global, repeatable, and logical process to effectively resolve any issues arising from the instal

Manufacturing Engineer

Q1 Technologies, Inc.

Salt Lake City, Utah, USA

Full-time

Manufacturing Engineer Salt Lake City, UT Job Description: 5+ years of experience & demonstrated proficiency in manufacturing, Process validation & providing ongoing technical support is preferred with evidence of continued self-development. Work experience in the Medical Device industry. Must Have Technical/Functional Skills In-depth knowledge of FDA regulations, Industry standards, and guidelines such as ISO 13485 and ISO 14644. Experience in control facility, warehouse and cleanroom validati