61 - 80 of 609 Jobs

Principal Regulatory Consultant Dietary Supplements

Apptad Inc

New Jersey, USA

Contract, Third Party

Job Description: Job Title: Principal Regulatory Consultant Dietary Supplements (U.S.-Based) Position Type: Contract / Consulting Location: Jersey City, NJ Department: Regulatory Affairs / Corporate Development Position Summary: We are seeking a highly experienced and credentialed Regulatory Consultant to support strategic M&A due diligence initiatives within the dietary supplement industry. This role demands deep understanding of the U.S. regulatory landscape, including DSHEA, FDA cGMPs (21 CFR

Clinical Research Associate I (Onsite), Ramin Lab

CEDARS-SINAI

Los Angeles, California, USA

Full-time

Job Description This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensur

Database Architect

Stellar IT Solutions

St. Louis, Missouri, USA

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

Job Title: Database Architect Location: St. Louis, MO (Onsite) Job Type: Long-term Contract Industry: Pharmaceutical / Healthcare (FDA-regulated environment) Summary: We are seeking a seasoned Database Architect with expertise in Oracle and SQL Server to oversee and optimize our enterprise database environments hosted at a third-party data center. This position will manage the hosting partner to ensure SLA adherence, assist with architectural decisions, and support application teams in build

Clinical Research Associate I (Onsite), Ramin Lab

CEDARS-SINAI

Los Angeles, California, USA

Full-time

Job Description This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensur

Principal Engineer

Katalyst Healthcares and Lifesciences

Plymouth, Minnesota, USA

Full-time

Job Description: This section focuses on the main purpose of the job in one to four sentences. Technical lead for DHF structure within sustaining engineering for disposable medical devices. Responsibilities: This section contains a list of primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned. Manage a new 3rd-party supplier documentation strategy for peritoneal dialysis disposable sets. Manage change controls from init

Development Process Engineer

Experis

Saint Paul, Minnesota, USA

Full-time

Title: Development Process Engineer Location: St. Paul, MN (100% Onsite) Duration: 12 Months Pay Range : $30/hr to $33/hr (On W2) We are looking for a "Development Process Engineer" to join one of our Fortune 500 clients. Job Responsibilities: Establish processes based on product specifications, evaluate process and design alternatives based on Design for Manufacturability principles Understand principles of Cost of Goods Sold, manage program compliance with Quality Control requirements (i.e.

CSV Engineer

Katalyst Healthcares and Lifesciences

Raritan, New Jersey, USA

Full-time

Roles & Responsibilities: 7-10 years' experience in Computer System Validation of SAAS systems, and Cloud systems. Must have experience in Agile methodology and handled multiple releases in parallel. Has working experience in any one or two of the following domains Tool validation like Service NOW, Automation tools, JIRA. Guide the project team with the right set of applicable project deliverables based on project type and category while catering to the SDLC. Application of FDA guidance's a

Clinical Research Associate I - (Hybrid)

CEDARS-SINAI

Beverly Hills, California, USA

Full-time

Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research

Sr. Biostatistician needed for Remote Job longterm Contract!!!

Nam Info Inc

Remote or US

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 : Sr. Biostatistician Location:Remote Duration : 6+ months contract EST time zone- candidate need to work in EST time Skills: At least 8years of experience In Addition to the above Statistical Programming II experience Lead statistica

IRT Auditor

I.T. Solutions

Remote

Contract

Role: IRT Auditor Location: Remote Type: Contract Length: 6 months Position Summary: We are seeking an experienced Oncology QA Auditor with a strong background in clinical quality assurance and a solid understanding of AI-driven technologies used in clinical trials. This role is essential to ensuring compliance across oncology programs that leverage artificial intelligence and machine learning (AI/ML) tools for clinical decision support, trial optimization, and real-world data interpretation.

SAP SSAM (Service and Asset Management) Consultant :: C2C

Trebecon LLC

Jersey City, New Jersey, USA

Contract, Third Party

Role: SAP SSAM (Service and Asset Management) Consultant Location: Hybrid, New Jersey Experience Level: Senior (10+ years) Job Description: We are seeking an experienced and certified SAP SSAM (Service and Asset Management) Consultant to lead and support the implementation, optimization, and support of SAP SSAM solutions within a regulated industry environment. The ideal candidate will have deep functional and technical knowledge of SAP EAM (Enterprise Asset Management) and SAP SSAM, along wi

CSV Engineer

Katalyst Healthcares and Lifesciences

Santa Clara, California, USA

Full-time

Job Description: The CSV Engineer will play a critical role in ensuring that all computerized systems used in the manufacturing and quality systems of medical devices are validated according to applicable regulations such as FDA 21 CFR Part 11, EU Annex 11, and ISO 13485. This role ensures the systems are compliant, reliable, and fit for intended use, supporting quality and regulatory requirements across the organization. Responsibilities: Develop and execute Computer System Validation (CSV) de

SAP SSAM (Service and Asset Management) Consultant :: Hybrid

Trebecon LLC

Jersey City, New Jersey, USA

Contract

Role: SAP SSAM (Service and Asset Management) Consultant Location: Hybrid, New Jersey Duration: 6 months to 1 year Industry: Life Sciences / Pharmaceuticals / Medical Devices Experience Level: Senior (10+ years) Job Description: We are seeking an experienced and certified SAP SSAM (Service and Asset Management) Consultant to lead and support the implementation, optimization, and support of SAP SSAM solutions within a regulated industry environment. The ideal candidate will have deep functi

Mechanical Engineer

Jobot

Vista, California, USA

Full-time

Excellent Opportunity to Join a Fast Growing Manufacturing Company! Competitive Salary and Stellar Benefits! This Jobot Job is hosted by: Jaclyn D'Amore Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $85,000 - $100,000 per year A bit about us: We are seeking an experienced Manufacturing Engineer with a strong background in project management and regulated manufacturing environments. This individual will drive continuous improvement, optimi

SeniorConsultant -Clarity LIMS

Recruitment.ai

San Francisco, California, USA

Full-time

Job Title: Senior Consultant - Clarity LIMS Location: Bay Area, CA (Onsite) About the RoleWe are seeking a highly experienced Clarity LIMS Developer to lead the design, configuration, customization, and integration of Illumina s Clarity Laboratory Information Management System (LIMS). The ideal candidate will have experience in LIMS development, with significant expertise in Clarity LIMS, preferably in a regulated or high-throughput laboratory environment. Key ResponsibilitiesSystem Design & Co

Validation Support Engineer

Katalyst Healthcares and Lifesciences

Boston, Massachusetts, USA

Full-time

Job Description: We are seeking an experienced Validation Support Engineer to lead validation activities for Beckhoff Twin CAT PLC-controlled systems in a 24/7 GMP-regulated manufacturing environment. The role focuses on ensuring compliance with FDA regulations (21 CFR Part 11, 210, 211, 820), GAMP5 methodologies, and internal quality standards. Responsibilities: Develop/update Validation Plans (VP) and Master Validation Plans (MVP). Lead GxP risk assessments for system changes. Author and

Senior Supplier Quality Engineer

Jobot

Aurora, Colorado, USA

Full-time

Full-Time & Direct Hire Senior Supplier Quality Engineer needed for Global Health-Tech Leader! This Jobot Job is hosted by: James Thai Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $90,000 - $120,000 per year A bit about us: Based in Colorado Springs, CO, we are reimagining healthcare through breakthrough technologies and human-centered design. Our company is a global leader in health innovation, creating smart systems that improve lives

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,

Computer System Validation (CSV) Engineer

Katalyst Healthcares and Lifesciences

Remote or Massachusetts, USA

Full-time

Responsibilities: Lead and execute CSV activities across GxP-regulated systems (LIMS, MES, ERP, etc. Author and maintain validation deliverables: URS, FS, DS, IQ, OQ, PQ, and traceability matrices. Ensure systems comply with 21 CFR Part 11, EU Annex 11, and GAMP 5. Support system implementations, upgrades, and periodic reviews. Collaborate with QA, IT, and business users to drive validation strategy. Participate in audits and inspections to demonstrate compliance. Requirements: Bachelor's

Senior Continuous Improvement Engineer

Experis

Pleasanton, California, USA

Full-time

Title: Senior Continuous Improvement Engineer Location: Pleasanton, CA (100% Onsite) Duration: 12 Months Pay Range : $55/hr to $59/hr (On W2) We are looking for a " Senior Continuous Improvement Engineer" to join one of our Fortune 500 clients. Job Summary: We're hiring a Senior Continuous Improvement Engineer to lead Lean, Six Sigma, and process improvement initiatives across manufacturing operations. This role works closely with cross-functional Value Stream teams to improve quality, cost, de