| Resume alert | Resumes 81 - 90 of 209 |
Director, Product development
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
... 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
Process Engineer Chemical Engineering
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
... 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
Customer Service Manager
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
... 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
Engineering Manufacturing
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
... 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
Quality Management, Process Validation
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
... 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
Senior Manager R&D Bioinformatics
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
... 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
Quality Assurance Automation Engineer
Vista, CA
... Revised the Standard Operating Procedures to make IT FDA Compliant using Official FDA Documents for Reference. Input Discrepancy Reports on new problems found using Jira and ClearQuest. Wrote Test cases and automated them based on Requirements ... - 2015 Jun 17
... Revised the Standard Operating Procedures to make IT FDA Compliant using Official FDA Documents for Reference. Input Discrepancy Reports on new problems found using Jira and ClearQuest. Wrote Test cases and automated them based on Requirements ... - 2015 Jun 17
Engineer Quality
Temecula, CA
... Worked as FDA liaison on MD-11 program. . 200 hours of training in scheduling, problem solving and continuous improvement. - 2015 Apr 14
... Worked as FDA liaison on MD-11 program. . 200 hours of training in scheduling, problem solving and continuous improvement. - 2015 Apr 14
Quality Medical Device
Escondido, CA
... Expertise in complaint handling, MDR triage and filing through FDA, CAPA Initiation/Implementation/VOE/Closure, NCMR classification, and Quality Software design. Highly efficient using Excel/ PowerPoint to take data from CAPA, Complaints, NCMR, and ... - 2015 Jan 31
... Expertise in complaint handling, MDR triage and filing through FDA, CAPA Initiation/Implementation/VOE/Closure, NCMR classification, and Quality Software design. Highly efficient using Excel/ PowerPoint to take data from CAPA, Complaints, NCMR, and ... - 2015 Jan 31
Buyer, Planner, Inventory Control Specialsit
Encinitas, CA
... • Adhere to ISO standards & FDA compliance for Medical Device industry. PROFESSIONAL EXPERIENCE BREG INC., Carlsbad, CA 2012 2014 MRO Buyer/Supply Chain Planner • Logistics & Brokerage negotiations resulting in $150,000 annual savings. • Negotiated ... - 2014 Oct 30
... • Adhere to ISO standards & FDA compliance for Medical Device industry. PROFESSIONAL EXPERIENCE BREG INC., Carlsbad, CA 2012 2014 MRO Buyer/Supply Chain Planner • Logistics & Brokerage negotiations resulting in $150,000 annual savings. • Negotiated ... - 2014 Oct 30