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Resumes 101 - 110 of 495 |
Union City, CA
... Mountainview, CA Executive IT Consultant 2/2019 – 9/2019 Provider of the first FDA cleared and CE marked MRI-Guided Radiation Therapy cancer treatment system Consulted on development of in-house IT capabilities for public company as it enters hyper ...
- 2020 Mar 11
Castro Valley, CA
... Trained and certified in GMP/FDA, Clean room Suites and Analytical Laboratories. Duties include performing formulations and assisting in production goals, sterilizing instruments, storing along with accurate documentation of work performed. Bio ...
- 2020 Jan 28
San Francisco, CA
... ● Prepare and maintain documents for FDA reviewers, ISO reviewers, and auditors. ● Review and finalized CofA and product specification sheets. Education Computer Software Engineering – Hack Reactor Bachelor of Science: Pharmaceutical Chemistry, June ...
- 2020 Jan 24
San Ramon, CA
... with Philips for Application Maintenance and Support and “unique device identifier” (UDI) Implementation, this project is related to FDA compliance intended primarily to provide information about submitting data to the database for device Labelers. ...
- 2019 Nov 05
Castro Valley, CA
Elson Young Mobile Phone: 510-***-**** ● Email: adajxv@r.postjobfree.com Objective Highly experienced Quality Assurance professional seeking a position in an organization where I can utilize my skills, experience, and knowledge towards FDA and ...
- 2019 Oct 09
Vallejo, CA
... Hyper-V Virtual-servers for monitoring dashboards - wall-monitors, Solarwinds, Event Log Analyzer Coordinated IT Operations to design, manage and deploy server environments Maintained GxP documentation vault for FDA audits Select Staffing S.B. ...
- 2019 Oct 01
Hayward, CA
... Validation lead for IT team confirming to FDA requirements with HPQC and Valgenesis systems. Accomplishments Sales force implementation needed a scrum master as well as a Business Analyst for the regulatory track. Learned SalesForce and led the 70 ...
- 2019 Aug 22
Dublin, CA
... Reddy’s - Shreveport, Louisiana – 2013-2017 Operations Manager for Oral Solid Dose Managed twelve employees responsible for the Coating, Printing & Packaging Operations Ensured adherence to all FDA guidelines and regulatory compliance Project leader ...
- 2019 Aug 21
San Francisco, CA
... Manage clinical laboratory testing for Pathology Research, including all sources of laboratory samples, SOPS write-up procedure, supplies, and studies performed in compliance with FDA good laboratory Practice regulation. Research Development - ...
- 2019 Jul 03
San Ramon, CA
... Excellent knowledge in FDA and EMA regulations and cGMP, ICH guidelines (Q8, Q9, Q12) Knowledge of writing standard operating procedures (SOPs), data capture and quality review, analytical methods, assay validation, and documents for regulatory ...
- 2019 Jun 10