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Resumes 41 - 50 of 321 |
Alpine, CA
... FDA 21 CFR Part 820 Program, CDMO’s, NCMR’s Program, CAPA Program, SCAR Program, OEE Program, FMEA Program. TPS, 6 “S’s”, 8 Mudas, Gemba walks to find Kaizen events specially for EHR, VSM, Validations: IQ, OQ, PQ Program. Root cause analysis, Cause ...
- 2023 Nov 12
National City, CA, 91950
... and leveraging social media advertising Ensure full compliance with sanitation and safety regulations, as mandated by the FDA and other relevant authorities, to uphold the highest standards of food safety and customer well-being Coordinate day-to ...
- 2023 Nov 09
San Diego, CA
... Led compliance remediation program, FDA audit readiness initiatives, identifying risks and driving CAPA resolutions. Experience in spinal surgery medical devices, implants, and electro/mechanical medical devices. Utilize Six Sigma Model DMAIC & DFSS ...
- 2023 Oct 30
San Diego, CA, 92101
... Followed established Standard Operating Procedures, GMP and ISO 9000 practices under FDA regulated environment. Bachem, Torrance, CA 08/2001 - 03/2002 Chemist : Purification of crude peptide through the use of preparative HPLC’s/ Beckman, including ...
- 2023 Sep 30
San Diego, CA
... SKILLS: *SAP-LMS *Made2Manage EDMS *Agile EDMS *eDocS EDMS *NovaManage EDMS *TeamCenter *Cisco Certified Network Associate (CCNA) *Documentum *GXP Documentation * ISO 9002, ISO 13485/EN 46000, ISO 13488/EN 46002 standards and FDA related regulations ...
- 2023 Sep 28
San Diego, CA
... This test has not been FDA cleared or approved. This test has been authorized by FDA under an Emergency Use Authorization (EUA). This test is only authorized for the duration of time the declaration that circumstances exist justifying the ...
- 2023 Sep 08
San Diego, CA
... Certificate – Mayo Clinic Laboratories OSHA Bloodborne Pathogen Training - Certificate Good Clinical Practices – CITI Program US FDA Focus US FDA Focus GCP for Clinical Trials with Investigational Drugs and Medical Devices US FDA Focus - Certificate ...
- 2023 Sep 07
Santee, CA
OMID SOURESRAFIL Del Mar • 612-***-**** • adzhvo@r.postjobfree.com Medical Device Clinical/Regulatory Expert Senior Medical Device Consultant •in Regulatory Affairs, FDA, EU MDR, 510(k) PMA, Chief Technology Officer • CEO Senior Clinical Research ...
- 2023 Sep 05
San Diego, CA, 92127
... • Evaluate and administer all phases of clinical studies • Liaise with pharmaceutical company representatives to ensure projects are completed on time, within budget, and in compliance with SOP, FDA, OHRP regulation, and ICH/GCP guidelines. ...
- 2023 Aug 13
San Diego, CA
... • Organization of files • Basic marketing Skills • Pharmaceutical calculations • Medical & Pharmaceutical Terminology • FDA Compliance • Customer Service & Relationship Building • Proficient in Microsoft Word, PowerPoint, Excel • Exhibit team ...
- 2023 Jul 24