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Validation EngineerJob Title - Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

Remote QA Manager with Healthcare Payer and Claims expJob Title - Remote QA Manager with Healthcare Payer and Claims exp

Infinite Computer Solutions (ICS)Company Name - Infinite Computer Solutions (ICS)

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Remote

Full-time

Note : GCEAD, L2EAD, consultant can apply for this position who can work on W2. Job Summary: We are looking for an experienced QA Healthcare Manager to lead the quality assurance team in ensuring the reliability, security, and compliance of healthcare applications. The ideal candidate should have a strong background in healthcare software testing, regulatory compliance (HIPAA, CMS, FDA), test automation, and team leadership. Key Responsibilities: we need someone who understand healthacre paye

Senior Clinical SAS programmer with Pharma experience -Remonte-W2 -ContractJob Title - Senior Clinical SAS programmer with Pharma experience -Remonte-W2 -Contract

BiogensysCompany Name - Biogensys

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Remote

Contract

Biogensys is currently hiring a Senior SAS programmer with Pharma experience for 6 to 12 months contract on w2. This is a remote position, no corp to corp, or 1099. No sponsorship is available. Statistical Programmer II: Pharma experience/Remote At least 7-8 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

Sr. Instrument Verification and Validation EngineerJob Title - Sr. Instrument Verification and Validation Engineer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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Rochester, New York, USA

Full-time

Responsibilities: Designing and implementing software of embedded devices and systems. Designing, developing, coding, testing, and debugging system software. Develop Requirements based manual test procedures. Access requirements for testability and determine best test approach. Compile and analyze test results. Document and manage system software defects. Participate in regular scheduling and team meetings. Participate in regular off hour meetings with partner in China. Understand projec

Product Security EngineerJob Title - Product Security Engineer

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

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Third Party, Contract

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

Senior C++ QT Software Engineer - Med DeviceJob Title - Senior C++ QT Software Engineer - Med Device

Motion Recruitment Partners, LLCCompany Name - Motion Recruitment Partners, LLC

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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

Packaging SupervisorJob Title - Packaging Supervisor

Mice GroupsCompany Name - Mice Groups

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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

Senior Manufacturing Engineer - Beverage Experience Highly PreferredJob Title - Senior Manufacturing Engineer - Beverage Experience Highly Preferred

JobotCompany Name - Jobot

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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

Sr. Principal StatisticsJob Title - Sr. Principal Statistics

PARAKEET WORLD SOLUTIONS LLCCompany Name - PARAKEET WORLD SOLUTIONS LLC

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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

Engineering Documentation ExpertJob Title - Engineering Documentation Expert

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

Senior Staff, Software Quality Assurance EngineerJob Title - Senior Staff, Software Quality Assurance Engineer

StrykerCompany Name - Stryker

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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

Engineer Disposables R&D, SustainingJob Title - Engineer Disposables R&D, Sustaining

StefaniniCompany Name - Stefanini

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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.

Principal Engineer Disposables R&D, SustainingJob Title - Principal Engineer Disposables R&D, Sustaining

StefaniniCompany Name - Stefanini

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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

Sr. Validation & Verification EngineerJob Title - Sr. Validation & Verification Engineer

ConsultNet, LLCCompany Name - ConsultNet, LLC

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Salt Lake City, Utah, USA

Full-time

Sr. Verification & Validation Engineer (onsite) Salt Lake City, UT Contract to hire Pay: $50-$65/hr Job Description: We are looking for a Senior Verification and Validation (V&V) Engineer to lead the development and execution of our testing strategy across hardware, embedded software, and clinical software systems. In our fast-paced startup environment, this role will be critical in planning, executing, and documenting V&V activities to ensure the safety, effectiveness, and regulatory compliance

Statistical Programmer needed for Remote Job only EST candidates needed!!!Job Title - Statistical Programmer needed for Remote Job only EST candidates needed!!!

Nam Info IncCompany Name - Nam Info Inc

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Remote or US

Full-time, Third Party, Contract

Dear, Hope you are doing well. Send resumes along with expected bill rates on W2( NO Benefits) or Independent contractors only apply and share to Note : NO 3rd party candidates, or H1's/EAD's/OPT's please. Role :Statistical Programmer II Location :Remote Duration : 6+ months contract EST ZONE CANDIDATES ONLY Statistical Programming II: Key responsibilities At least 5 years of experience in ADaM/TLF. Create, validate, and maintain SAS programs for data analysis, reporting, and submission de

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

Senior SAS ProgrammerJob Title - Senior SAS Programmer

Katalyst Healthcares and LifesciencesCompany Name - Katalyst Healthcares and Lifesciences

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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

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

Labeling Design SMEJob Title - Labeling Design SME

InvolgixCompany Name - Involgix

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Irving, Texas, USA

Third Party, Contract

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