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SAP Analytics Cloud (SAC) Consultant Pharma Domain

RigelSky Inc

•

Remote

Contract, Third Party

SAP Analytics Cloud (SAC) Consultant Pharma Domain Role Overview We are seeking an experienced SAP Analytics Cloud (SAC) Consultant to support analytics and reporting initiatives for a leading pharmaceutical client. The role focuses on building scalable dashboards, visualizations, and data models that enable insights across clinical operations, regulatory compliance, and commercial performance. Key Responsibilities Design and develop SAC stories and dashboards tailored to pharmaceutical business
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Posted 4 hours ago

Mid Level Full Stack Developer -W2-FULL TIME ONLY (NO H1B/OPT/CPT EAD)

Paladin Consulting, Inc.

•

Dallas, Texas, USA

Full-time

Job Title: Mid-Level Java Full Stack Engineer Work Location: Remote Education/Experience Required: Bachelors degree in Computer Science or related field; Three (3) years of experience working in a SaaS-based product development environment or FDA-regulated medical device environment; experience working with AWS is a plus Job Description & Responsibilities : Designs, develops, and maintains web applications across both front-end and back-end systems.Works with technologies such as Java, Angular,
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Posted 15 days ago | Updated 15 days ago

Manufacturing Engineer Medical Device

RAPS Consulting Inc

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Sarasota, Florida, USA

Contract

Hi, Hope you are doing well. We are currently sourcing for multiple Manufacturing Engineer roles with a strong focus on Medical Device manufacturing and validation protocols (IQ/OQ/PQ). Role: Manufacturing Engineer Location: Gainesville, FL & Sarasota, FL (Onsite) Duration: Long Term Contract Experience: 8+ Years (Medical Device Mandatory) Required Skills: IQ/OQ/PQ validation experience in medical parts manufacturing8 10 years of relevant process validation & manufacturing experienceMedical Devi
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Posted 4 days ago

Sr. Instrument Verification and Validation Engineer

Katalyst Healthcares and Lifesciences

•

Rochester, New York, USA

Full-time

Job Description: Client is seeking a Verification and Validation SR Engineer to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements based manual test case design and execution of test procedures in a BL2 lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with so
Posted 36 days ago | Updated 4 hours ago

Sr. Toxicology Associate Remote

Generis TEK Inc.

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Remote or Racine, Wisconsin, USA

Contract

We have Contract role Sr. Toxicology Associate-Remote for our client at Racine WI. Please let me know if you or any of your friends would be interested in this position. Position Details: Sr. Toxicology Associate-Remote-Racine WI Location : Racine, WI 53403 (Remote) Project Duration : 10+ Months Contract REQUIRED EDUCATION: PhD or Master s degree in toxicology or a related field TOP 5 REQUIRED SKILLS: 1. 4+ years of human health risk assessment experience 2. Proficiency in toxicity study proto
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Posted 4 days ago | Updated 18 hours ago

Senior Regulatory Affairs Specialist

ZennSoft

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Union City, California, USA

Full-time

Job Title: Senior Regulatory Affairs (RA) Specialist Location: Union City, CA Industry: Medical Devices / Regulatory Affairs Employment Type: Full-Time Client: Lhasa OMS, Inc. About the Role Lhasa OMS, Inc. is seeking a highly motivated Senior Regulatory Affairs Specialist to join our team in Union City, CA. The ideal candidate will support the Regulatory Affairs department by preparing and submitting regulatory documentation for medical devices in both domestic and international markets. This p
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Posted 21 days ago

Controls Validation Engineer

BEPC, Inc.

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Irvine, California, USA

Contract

Summary Join our team as an Electrical/Controls Engineer specializing in IT and equipment validation for cutting-edge medical device manufacturing. In this role, you will support Lifesciences Plant Operations Engineering by leading and executing validations for PLCs, SCADA systems, and other manufacturing equipment. You ll work cross-functionally with engineering, quality, validation, and regulatory teams to ensure compliance with FDA, ISO 13485, and 21 CFR Part 11 standards. This position blen
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Posted 1 day ago

Senior Mechanical Engineer - Med Device

Motion Recruitment Partners, LLC

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Boston, Massachusetts, USA

Full-time

Our client, an established global leader in the diagnostics and medical device sector, is currently seeking a Senior Mechanical Engineer to join their growing R&D team. This role offers the opportunity to work on advanced diagnostic instruments and devices that directly impact patient care and clinical outcomes. Key Responsibilities: Lead the design and development of mechanical components and subsystems for complex medical devices, from concept through to production.Collaborate with cross-fun
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Posted 59 days ago | Updated 12 hours ago

CSV Lead

Prudent Technologies and Consulting

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Raritan, New Jersey, USA

Third Party, Contract

Role - CSV Lead Location - Raritan, NJ(Hybrid) Job Details: 7-10 years experience in Computer System Validation of EMS and BMS applications Must have experience in Agile methodology and handled multiple releases in parallel Extensive knowledge in CSV, CSV auditing, creation and revision of CSV documentation, experience with EMS/BMS, project management, test script review, test execution review, test defect management. Has working experience in any one or two of the following domains Tool val
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Posted 11 days ago

Oracle Argus Engineer

Spotline

•

Alameda, California, USA

Contract, Third Party

Senior Oracle Argus Engineer Alameda CA Onsite role Job Description: Manage implementation/upgrade/support of Oracle Argus Safety System or other Safety solutions and associated interfaces/integrationsPart of technical workstreams (Configuration/Data Migration/Reporting/Upgrade) and provide progress reports, proposals, requirements documentation, and presentations.As Oracle Argus SME, support technical issues associated with Oracle Argus Safety suite and related interfacesHelp deliver project an
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Posted 20 days ago | Updated 13 days ago

Senior Validation Engineer

Takeda pharmaceutical

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Lexington, Massachusetts, 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
Posted 22 days ago | Updated 4 hours ago

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
Posted 15 days ago | Updated 4 hours ago

Validation Engineer

Merck KgaA

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Miamisburg, Ohio, USA

Full-time

Work Location: Miamisburg, Ohio Shift: No Department: LS-SC-PEMM Engineering & Maintenance Recruiter: Renay Middleton Hiring Manager: John Shay This information is for internals only. Please do not share outside of the organization. Your Role: In this role you will develop and execute validation protocols to ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements. This role is crucial for maintaining the quality and integrity of manufacturing processes and produ
Posted 22 days ago | Updated 4 hours ago

Engineering - Non Degreed I - 2nd Shift

BEPC, Inc.

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El Pueblito, Querétaro, Mexico

Contract

BEPC inc is seeking a Non-Degreed Test Technician for 2nd shift in the Irving, TX area! W2 contract: 12 months w/ possible extensions Pay rate: $!9 - $21.29/hr Benefits: Medical, Dental, Vision & Life Insurance Shift: 12pm - 12:30am Working under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing env
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Posted 12 days ago

Engineering - Non Degreed I - 2nd Shift

BEPC, Inc.

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El Pueblito, Querétaro, Mexico

Contract

BEPC inc is seeking a Non-Degreed Test Technician for 2nd shift in the Irving, TX area! W2 contract: 12 months w/ possible extensions Pay rate: $!9 - $21.29/hr Benefits: Medical, Dental, Vision & Life Insurance Shift: 12pm - 12:30am Working under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing env
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Posted 12 days ago

Design Quality Engineer

Thunderhawk Technology Partners

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North Haven, Connecticut, USA

Full-time, Contract

Job Description: * Evaluate product issues to ensure patient, user and security risk are assessed, and acting as the lead Design Quality Engineer for Post-Market Design Changes on Capital Hardware * Update DFMEA and DHF documents as needed as part of the post market design change management process * Provide comprehensive support to Post Market Development Teams with a focus on Design Quality and Risk Management * Collaborate with different departments across the organization to understand and
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Posted 15 days ago | Updated moments ago

Senior Manufacturing Engineer - Beverage Experience Highly Preferred

Jobot

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Lewisville, 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 2 days ago | Updated moments ago

Validation Engineer

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
Posted 10 days ago | Updated 4 hours ago

Remote QA Manager with Healthcare Payer and Claims exp

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
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Posted 28 days ago | Updated 18 days ago

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

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
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Posted 14 days ago