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Product Security Engineer

E-Solutions, Inc.

•

US

Contract, Third Party

Role: Product Security Engineer Location: Remote Deliver documentation for pre-market product development activities including security plans, architecturediagrams, data fl ow diagrams, threat models, security requirements, Design for Security, SBOM, and risk management documentation. Drive and monitor and post-market vulnerability management activities, with adherence to strict timelines. Support compliance certification activities, such as SOC2, FedRAMP, ISO 27001, etc. Job description + ye
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Posted 32 days ago | Updated 5 hours ago

Packaging Supervisor

Mice Groups

•

Livermore, California, USA

Full-time

Job Title: Packaging Supervisor Salary Range: $68,000 $80,000 Shift Preference: Swing shift preferred, but day shift is also an option Job Summary: The Packaging Supervisor oversees employees in a manufacturing and assembly setting. Responsibilities include planning work, enforcing safety and food standards, and improving production processes. Key Duties: Implement and manage production schedulesAssign and supervise line personnelCommunicate with staff about performance, scheduling, and qualityM
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Posted 2 days ago

Senior C++ QT Software Engineer - Med Device

Motion Recruitment Partners, LLC

•

Marlborough, Massachusetts, USA

Full-time

Our client, a leading innovator in the medical device industry, is seeking a Senior Software Engineer with strong expertise in C++, Qt, and image processing/computer vision. This role offers the opportunity to contribute to advanced diagnostic and imaging solutions that have a real impact on patient care. Key Responsibilities: Design, develop, and maintain software applications using C++ and the Qt frameworkImplement and optimize algorithms for image processing and computer visionCollaborate wit
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Posted 28 days ago | Updated 2 hours ago

Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLC

•

Remote

Contract

Job Title: Sr. Principal StatisticsLocation: Remote Duration: 6 MonthsEmployment Type: W2 ContractExperience Level: Mid-SeniorEducation Required: Ph.D. or MS in Statistics or BiostatisticsIndustry: Pharmaceuticals Job Summary:The Sr. Principal Statistician will lead statistical activities in clinical trials, from protocol development to final study reporting. The role will also contribute to regulatory filings, in-licensing evaluations, and marketing support. Key Responsibilities:Review protocol
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Posted 13 days ago

Engineering Documentation Expert

Katalyst Healthcares and Lifesciences

•

Fort Worth, Texas, USA

Full-time

Responsibilities: Develop comprehensive technical documentation, including user manuals, installation guides, labeling materials, and regulatory documentation for ophthalmic devices. Work closely with engineering, regulatory, and quality teams to ensure all documentation meets industry standards and regulatory requirements. Interpret engineering drawings and specifications to create detailed build and qualification procedures for complex ophthalmic systems. Collaborate with R&D and manufacturing
Posted 60+ days ago | Updated 6 hours ago

Senior Staff, Software Quality Assurance Engineer

Stryker

•

Portage, Michigan, USA

Full-time

Work Flexibility: Hybrid Senior Staff, Software Quality Assurance Engineer Stryker is seeking a Senior Staff Software Quality Assurance Engineer to support our Digital Robotics and Enabling Technologies business by driving quality processes. In this role, you will partner with R&D software development teams to guide them through internal quality system processes and ensure compliance with regulatory standards, including FDA, HIPAA, ISO, and SOC 2. Work Flexibility: Hybrid: Candidates must resi
Posted 2 days ago | Updated 6 hours ago

Engineer Disposables R&D, Sustaining

Stefanini

•

Plymouth, Minnesota, USA

Contract

Stefanini Group is hiring! Stefanini is looking for Engineer - Disposables R&D, Sustaining in Plymouth, MN (Hybrid) For quick Apply, please reach out to Vipul Bhardwaj - call: / email: Work Hours: M-F (40 hours) Work Location: Plymouth, MN (Hybrid) Shift: 1st Shift Create new 3rd party supplier documentation including design specifications, labeling, design drawings, etc. for peritoneal dialysis disposable sets.Create, modify, and maintain design history files.Perform change control assessments.
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Posted 10 days ago | Updated 2 hours ago

Principal Engineer Disposables R&D, Sustaining

Stefanini

•

Plymouth, Minnesota, USA

Contract

Stefanini Group is hiring! Stefanini is looking for Principal Engineer - Disposables R&D, Sustaining in Plymouth, MN (Hybrid) For quick Apply, please reach out to Tuhin Podder- call: /email: Work Hours: M-F (40 hours) Work Location: Plymouth, MN (Hybrid) Shift: 1st Shift Technical lead for DHF structure within sustaining engineering for disposable medical devices.Manage new 3rd party supplier documentation strategy for peritoneal dialysis disposable sets.Manage change controls from initiation th
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Posted 10 days ago | Updated 2 hours ago

Software Engineer - C# & Python

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: Software Engineer Duration: 12 Months plus Location: Hybrid - Dallas, TX Job Descrip
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Posted 7 days ago | Updated 5 hours ago

Labelling Manager

Altezzasys

•

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
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Posted 11 days ago

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
Posted 17 hours ago | Updated 6 hours ago

Principal Engineer Disposables R&D, Sustaining

Pyramid Consulting, Inc.

•

Plymouth, Minnesota, USA

Contract

Immediate need for a talented Principal Engineer Disposables R&D, Sustaining. This is a 17+months contract opportunity with long-term potential and is located in Plymouth, MN (Hybrid). Please review the job description below and contact me ASAP if you are interested. Job ID:25-77915 Pay Range: $50 - $51/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan. Key Responsibilities: Manage new 3rd party supplier documentation strategy for p
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Posted 10 days ago

Senior Manufacturing Engineer - Beverage Experience Highly Preferred

Jobot

•

Coppell, Texas, USA

Full-time

Hands-On Role, Path to Engineering Director This Jobot Job is hosted by: Tracy Hann Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $100,000 - $135,000 per year A bit about us: We are a privately held manufacturer in the health and wellness industry, producing a broad portfolio of nutritional supplements, ready-to-drink beverages, and personal care items. With decades of experience and operations across the southern U.S., we manage the full
Posted 14 hours ago | Updated 2 hours ago

Labeling Design SME

Involgix

•

Irving, Texas, USA

Contract, Third Party

Please find below updated job details ,kindly share and Upload candidate profiles. 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 transfers. P
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Posted 14 days ago

Hiring- Software Engineer / R & D Software Engineer

Recruitment.ai

•

Tennessee City, Tennessee, USA

Contract

Job Title: Software Engineer / R&D Software Engineer Location: East Tennessee - Hybrid Position Summary Software Engineers and R&D Software Engineers to join a growing development team. These roles will involve designing and developing advanced medical imaging software solutions used in orthopedic diagnostics and computer-assisted surgery. As a member of our team, they will work in a collaborative, fast-paced environment where innovation and excellence are highly valued. You will play a key role
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Posted 10 days ago

Validation Engineer III

Katalyst Healthcares and Lifesciences

•

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
Posted 60+ days ago | Updated 6 hours ago

Quality Management Systems (QMS) Specialist (W2)

Sovereign Technologies

•

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
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Posted 33 days ago | Updated 5 days ago

Pharmacovigilance Quality & Compliance Lead (GVP)

Cosmic-I LLC DBA Northern Base

•

Smyrna, Georgia, USA

Contract

We are looking for an Pharmacovigilance Quality & Compliance Lead (GVP) responsible for implementing and maintaining a balanced, proactive, global approach to pharmacovigilance (PV) compliance, to join us in our R&D and Pharmacovigilance Quality team. About the role The Pharmacovigilance Quality & Compliance Lead falls with the Impact Quality team within R&D and Pharmacovigilance Quality. This position is a global role responsible for ensuring pharmacovigilance (PV) activities are conducted in
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Posted 13 hours ago

Commissioning and Qualification Engineer

Katalyst Healthcares and Lifesciences

•

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
Posted 60+ days ago | Updated 6 hours ago

Process Engineer

Katalyst Healthcares and Lifesciences

•

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
Posted 60+ days ago | Updated 6 hours ago