- Kelly Services (Groveport, OH)
- …inventories. Skills & Qualifications: + 10 years of Quality experience in an FDA regulated manufacturing environment. + BS Degree in a Science or Engineering ... discipline + Strong understanding of quality technology at a level normally acquired through completion of a CQE certification program desired. What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit.… more
- Medtronic (Minneapolis, MN)
- …with key industry bodies and where required, government agencies (ie, US FDA , Notified Bodies). + Experience with validating and monitoring controlled environments, ... process water systems, and/or various sterilization modalities (Ethylene Oxide (EO), Vaporized Hydrogen Peroxide (VHP), Moist Heat, Dry Heat, and/or Radiation). + Requires practical knowledge in leading and managing the execution of processes, projects and… more
- Actalent (Irvine, CA)
- …to read and interpret CAD drawings. + Experience interacting with regulatory agencies ( FDA , MoH, TUV, etc.). + Thorough knowledge of US and International Medical ... Device Regulations. + Strong knowledge of Quality Concepts (eg, CAPA, Audits, Statistics). + Strong project management skills and ability to manage multiple tasks simultaneously. + Ability to advocate for product excellence and quality. + Effective… more
- Medtronic (Lafayette, CO)
- …warrantee, service, and repairs. + Experience implementing and adhering to FDA and computer systems validation requirements. + Demonstrated leadership in achieving ... shared objectives in a matrix organization, managing cross-divisional initiatives, and cross-functional teams + Highly organized, outcome oriented with excellent planning skills. + Excellent leadership, presence, and executive communication skills (written and… more
- Kelly Services (Rosenberg, TX)
- …environment preferred. + Ability to read and interpret technical procedures, SOP's, GMP's and FDA regulations. + Ability to work with MS Word and Excel and able to ... write reports and perform data entry. + Strong communication skills, both written and verbal. + Strong attention to detail. + Ability to lift 25 pounds. Job Details Contract-to-Hire Monday-Friday, 8am-5pm Pay Rate: $20-24 per hour As part of our promise to… more
- Amazon (Seattle, WA)
- …life sciences compliance and regulatory standards such as GxP, CLIA, and the FDA approval process Amazon is an equal opportunity employer and does not discriminate ... on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during… more
- Astrix Technology (Springfield, MO)
- …+ Familiarity with Good Manufacturing Practices (GMP) and regulatory guidance (eg, FDA , EMA, ICH). + Experience using electronic quality systems (eg, TrackWise, ... Veeva Vault, or similar). + Prior experience mentoring or training personnel on deviation and CAPA processes. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion,… more
- Astrix Technology (The Woodlands, TX)
- …issues and keep shipments on track. Monitor applicable import regulations (HTS, FDA , TSCA, ISF, etc.) and assist with process improvements and compliance controls. ... **Import Compliance Specialist Qualifications/Requirements:** Bachelor's degree in supply chain, logistics, international trade, or related field. 5+ years of experience in international/import trade operations. Strong knowledge of USMCA and Country-of-Origin… more
- Insight Global (San Diego, CA)
- …or program management experience - Pharma/clinical background, familiar with FDA regulated environments preferred - Strong vendor management experience, working ... as a liaison between stakeholders and IT vendors to manage project roadmap, updates, and deadlines - Generative AI exposure - SDLC experience, knowledge of technical projects and implementations - Road mapping, project execution, executive management, change… more
- Colgate-Palmolive (Sanford, ME)
- …all batch, material, label, and in-process data with accuracy and neatness to meet FDA guidelines. **Keeping the Making Area and equipment clean and organized at all ... times is critical.** + Productivity - **Operate Making Area equipment** to achieve production targets with minimal waste and downtime. Cross-train to achieve mastery of all making system operations, material handling/documentation, and equipment set-up/routine… more
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