141 - 160 of 726 Jobs

Process Engineer / Process Consultant

VDart, Inc.

San Antonio, Texas, USA

Third Party, Contract

Job Title: Process Engineer / Process Consultant Location: San Antonio, TX (Onsite) Duration/Term: Long Term Contract Focus: We are looking for a knowledgeable Process Consultant to give solid advice in their field of Banking or Insurance. They will be responsible for analyzing a process/process model/function and providing a fresh perspective. You will discover the most suitable solutions, whether it is proposing a new IT system or implementing a full strategic plan. Relevant Experience as a Pr

Structures Build Engineer (Super Heavy Booster)

SpaceX

Texas, USA

Full-time

SpaceX was founded under the belief that a future where humanity is out exploring the stars is fundamentally more exciting than one where we are not. Today SpaceX is actively developing the technologies to make this possible, with the ultimate goal of enabling human life on Mars. STRUCTURES ENGINEER (STARSHIP) The Structures Subassemblies Build team is responsible for creating rapidly manufacturable assemblies for Starship and the Super Heavy Booster. The products built by the team range from

Validation Engineer

Katalyst Healthcares and Lifesciences

Libertyville, Illinois, USA

Full-time

Responsibilities: Lead validation efforts for injection molding machines, auxiliary equipment (e.g., dryers, chillers, robots), and integrated automation systems. Develop and execute validation protocols (SAT, FAT, IQ, OQ, PQ) for molding and downstream equipment. Support the qualification of new production lines involving injection-molded components. Perform process characterization, capability studies, and stability testing for moulded parts. Collaborate with tooling, manufacturing, and q

CQV Engineer

Katalyst Healthcares and Lifesciences

Remote or New Jersey, USA

Full-time

Job Description: We are seeking a highly motivated and experienced CQV Engineer to join PharmEng Technology, a leading global provider of engineering and consulting services to the pharmaceutical and biotechnology industries. The CQV Engineer will lead commissioning, qualification, and validation activities for new and existing pharmaceutical facilities and equipment. Responsibilities: Develop and execute commissioning, qualification, and validation protocols for new and existing pharmaceutical

Avionics Network Engineer

Jacobs

Houston, Texas, USA

Full-time

Are you passionate about human space exploration, understanding the origins of the universe, and working with a passionate and diverse team to make a difference? If you are, we need you! We need your talent, teamwork, and energy to help us achieve great things that inspire people all over the globe. We need you to bring creative ideas and diverse backgrounds to help us envision, shape, and deliver systems that will enable the exploration of space while benefiting people here on Earth. We are exc

GMP/Pharma Manufacturing Operator (2nd Shift)(ONSITE)

NetSource, Inc.

Raritan, New Jersey, USA

Contract

Please note that this is a 1-year contract. This role will be 2nd Shift 3pm 11:30PM / M F Requirements: GMP document experience. High School Diploma required; Bachelor s Degree preferred 3+ years of experience in medical device or pharmaceutical manufacturing Experience using SAP is preferred Proficient with using MS Office (Word, Excel, Outlook) Strong mechanical problem-solving ability and technical aptitude Ability to work independently with limited supervision and work as part of a team Able

Statistical Programmer

System Edge (USA) L.L.C.

Remote

Contract

Statistical Programmer Anywhere in US EST time zone- candidate need to work in EST time Key responsibilities At least 5 years of experience in ADaM/TLF.Create, validate, and maintain SAS programs for data analysis, reporting, and submission deliverablesDevelop analysis datasets (ADaM) and tables, listings, and figures (TLFs) to support statistical analysis in production side.Collaborate with statisticians and data managers to define dataset specifications and outputsEnsure compliance with inter

Manufacturing Engineer

AMETEK.Inc

Irwindale, California, USA

Full-time

The Manufacturing Engineer will be responsible to manage manufacturing redline updates of drawings and for the review and disposition of non-conforming products, components, materials, and assemblies. Essential Duties and Responsibilities: This position serves as a liaison between the engineering department and operations and will be the first contact within the engineering department for manufacturing questions and suggestions. Other duties may include feasibility and safety testing, research

Kubernetes Engineer

Beacon Systems, Inc

Dallas, Texas, USA

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: Kubernetes Engineer Duration: 12 Months plus Location: Hybrid - Dallas, TX Job Descr

Windchill Consultant

Teknikoz

Sunnyvale, California, USA

Contract, Third Party

PTC Arena Consultant Job Description:We are seeking a skilled and proactive PTC Arena Consultant with a minimum of 3 years of hands-on experience in Arena PLM/QMS systems. The ideal candidate will play a key role in supporting, configuring, and enhancing Arena PLM to meet our product development and compliance needs. You will collaborate with cross-functional teams including Engineering, Quality, Regulatory, and Manufacturing to ensure smooth implementation and ongoing optimization of Arena s

BULK MECHANIC - ALBANY, NY

Matheson Tri-Gas, Inc.

Albany, New York, USA

Full-time

Job DescriptionDIESEL MECHANICS/TECHNICIANS MATHESON one of the nation's leading bulk suppliers of liquefied gases. Our Diesel Mechanics perform repairs and scheduled preventative maintenance in accordance with DOT standards on both our tractors and cryogenic trailers. Other duties will include maintaining shop parts, ordering and inventory control, tire repairs/changes, light vehicle electrical and some welding. The ideal candidate will be able to problem solve and be flexible to the ever-chang

Enterprise Data Service Engineer

Takeda pharmaceutical

Exton, Pennsylvania, USA

Full-time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by

Sr. SAS Programmer

Katalyst Healthcares and Lifesciences

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

ATE Software Validation Engineer Medical Devices

Sureminds Solutions

Skaneateles Falls, New York, USA

Third Party, Contract

Job Title: ATE Software Validation Engineer Medical Devices Location: Skaneateles Falls, NY (Onsite) Duration : Long-Term Interview Mode : Video Job Description : Automatic Test Equipment (ATE) Software Validation Engineer Lead software validation efforts for ATE systems used in testing infusion pumps, patient monitors, or diagnostic devices.Develop validation protocols, test plans, scripts, and reports in alignment with FDA 21 CFR Part 820, Part 11, and ISO 13485. Key Responsibilities: Lead sof

Propulsion Engineer II - Valves BE3U

Blue Origin, LLC

Seattle, Washington, USA

Full-time

Application close date: Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We're working to develop reusable, safe, and low-cost space vehicles and systems within a culture of safety, collaboration, and inclusion. Join our team of problem solvers as we add new chapters to the history of spaceflight! This role is part of the Blue Origin Engines business unit, where

Propulsion Engineer III - Valves BE3U

Blue Origin, LLC

Seattle, Washington, USA

Full-time

Application close date: Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We're working to develop reusable, safe, and low-cost space vehicles and systems within a culture of safety, collaboration, and inclusion. Join our team of problem solvers as we add new chapters to the history of spaceflight! This role is part of the Blue Origin Engines business unit, where

Sr. Propulsion Engineer - Valves BE3U

Blue Origin, LLC

Seattle, Washington, USA

Full-time

Application close date: Applications will be accepted on an ongoing basis until the requisition is closed. At Blue Origin, we envision millions of people living and working in space for the benefit of Earth. We're working to develop reusable, safe, and low-cost space vehicles and systems within a culture of safety, collaboration, and inclusion. Join our team of problem solvers as we add new chapters to the history of spaceflight! This role is part of the Blue Origin Engines business unit, where

Senior SAS Programmer

Katalyst Healthcares and Lifesciences

Seattle, Washington, USA

Full-time

Responsibilities: The Senior 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 suppor

R&D Engineer with Medical Device

Katalyst Healthcares and Lifesciences

Irvine, California, USA

Full-time

Job Description: We are seeking a motivated and innovative R&D Engineer to support the design, development, and testing of medical devices in compliance with FDA and ISO standards. The ideal candidate will work closely with cross-functional teams to bring new products from concept to commercialization. Responsibilities: Design and develop medical devices and components from concept to production. Create design inputs, outputs, risk analysis, and test protocols. Perform design verification and

Sr. R&D Electrical Systems Engineer (Med Device)

Oxford Global Resources

Santa Clara, California, USA

Contract

Title: Sr. R&D Electrical Systems Engineer Length of Contract: 4-6 Months + possible extension Location: Santa Clara, CA Onsite only. Ideal Start Date: Targeting August 11 or August 18, 2025 Interviews: 2 rounds, 1 on 1 first round, panel second round (onsite if local and willing for second round) True Timeslots: Tuesday July 29 1pm-3pm PST Reason for Needing a consultant: The client requires hands-on electrical engineering support to assist with ongoing troubleshooting and root cause analysis e