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Resumes 71 - 80 of 203 |
San Clemente, CA
... Develop Purchasing control drawing to be used with the supply base that conforms to FDA traceability, materials pedigree requirements, validate Good Manufacturing Practices are in place and conform to product requirements. Develop ERP/MPS ...
- 2016 Nov 19
San Diego, CA, 92126
... Cost Containment, Continuous Improvement and TQM ERP Implementation, SAP, Oracle JDE, QAD, Epicor, AS400 cGMP, ISO, FDA, ITAR, CLIA, OSHA Staff Development and Leadership Mentor NOTEWORTHY ACCOMPLISHMENTS Business Unit Turn Around Start Ups, ...
- 2016 Sep 03
Escondido, CA
... Track record of adhering to FDA standards during testing procedures and through the documentation stage. Professional Experience QUADRANTS SCIENTIFIC, INC San Diego, California, United States -Laboratory Analyst September 2012 – Present Set up and ...
- 2016 Mar 30
Carlsbad, CA
... toward FDA submission Family obligations 2014 - 2015 AVIVA BIOSCIENCES CORPORATION, San Diego, CA 2012 - 2014 Executive Vice President Directed the overall strategy at a biotech firm with the goal of building sustainable revenue generation results. ...
- 2016 Mar 10
Vista, CA
... electronic medical records (EMR) and bill information Established new product introduction procedures and policies for FDA and other regulatory bodies design guidelines, which impact the broader development Provide fostering environment for ...
- 2016 Feb 10
Oceanside, CA
... API Tech, International Medication Systems., Ltd 07/2009 – 10/2011 Followed the batch record from R&D to perform mixture of substances intended to be used in the manufacture of high purity active pharmaceutical ingredients (API) regulated by FDA. ...
- 2015 Dec 28
Oceanside, CA
... Test steps had to conform to GSDM and FDA guidelines. •Deployed 500+ Treo 750 handhelds nationwide to the sales force in deployment trainings setup across 7 cities. Provided onsite technical support and training. Created deployment and support plan ...
- 2015 Nov 06
Escondido, CA
... Strategic Experience -Training engineering and manufacturing teams -Development of strategic and tactical documents for senior and executive management -FDA and Canada Health compliance document experience -ISO 9001 and ISO 13495 with Canadian ...
- 2015 Oct 14
Carlsbad, CA
... Board Coordinator, in-charge of identifying / final disposition of Deficient Materials Knowledgeable in CFR 21 part III (FDA) and FALCPA (Allergens) Lead/Team Member in hiring, training and mentoring of Scientists and Senior Scientists Subject ...
- 2015 Oct 13
Carlsbad, CA, 92011
... familiar working in a GCP, GMP and FDA environment; build strong relationships with departmental leaders throughout the company, and contribute to leadership decisions Scientific Role Oversee execution of Bioinformatics and IT infrastructure for ...
- 2015 Sep 08