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Online Resumes with "cfr"
Transportation coordinator, Logistics Coordinator,Traffic Manager, HAZMAT inspector and certifier
My future goals are pretty simple. I would like to find work leveraging my experience gain in the military as Departure/Arrival Airfield Control Group (D/AACG) OIC 9 Years, Dangerous Goods Adviser 10 Years (ADR,RID,IATA,DTR,CFR-49,DOT),Transportation of Hazardous Materials( DOD/CFR-49/ADR/RID ) 14 Years, Transportation Coordinator 14 Years ,Air load Planner 9 Years ,Hazmat OIC/Certifier 12 Years and apply it to the civili...
Tags for this Online Resume: traffic manager, HAZMAT, transportation coordinator, QA inspector, Emergency management
Quality Engineering Professional
I am looking to work for a company with some prestige. I would like to work ina stable and growing industry. I would like to work in medical devices or in renewble energies.
Ideal Companies: Suniva, Solarworld, Boeing
Tags for this Online Resume: ISO9000, APQP, TS16949, Lead Quality Auditor, FMEA, Control Plan, GRR, MSA, CAPA, 8D, 7 Step, SIx Sigma
Chemist
I have 14 years of experience in pharmaceutical industries. Results oriented individual with a track record of instituting and maintaining high levels of Quality Assurance and leadership. I’m seeking additional opportunities for professional development in consulting, validation, compliance or technical areas. Strong analytical and planning skills. Six Sigma Black Belt trained. Knowledge in FDA, cGMP, GLP, 21 CFR - Part 820...
Ideal Companies: Pharmaceuticals or food industries
Tags for this Online Resume: qa, validation, lims, qc
Quality Assurance Associate Managert
Quality Assurance professional with problem-solving abilities in Pharmaceutical and Biotechnology industries. Primary strengths include US (FDA) 21 CFR, and ICH Q7A Guidance for API Manufacture, Quality Systems development and implementation and strong auditing skills. Introduced and managed electronic document management software including validation, implementation, and maintenance, as well as project team leadership. R...
Tags for this Online Resume: Quality Assurance, FDA regulations, CAPA, Document Control, Change control
Medical Affairs, Regulatory Affairs Associate, Clinical Affairs
Doctor of Medicine recognized with clinical trial expertise in medical device, drug safety, regulatory affairs, and post-market monitoring. Strong emphasis on utilization of cross-functional skills to advance medical systems and develop process improvements. Results-driven collaborator with effective oral and written communication and presentation skills. Patient advocate and contributor to public health awareness and educa...
Tags for this Online Resume: FDA MedWatch 21 CFR 820 803, Medical Device Class III, ICD, VT / VF, Medical Affairs, Regulatory Affairs, Drug Safety, Quality Assurance and Management, Public Health, Patient Relations, Medical Communication, SAP, Excel
Design/Develop/Sell/Manage/Travel
Outgoing personality with strong ability to solve changing business/industry needs with application/database development. Versatile, independent thinker with team attitude.
Ideal Companies: HP, IBM, IT SERVICES COMPANY, LOOKING TO MOVE INTO IT SALES
Tags for this Online Resume: JAVA, JSP, MySQL, SQL, SAS, Database, Programming, SQL Server, ACCESS, Microsoft Office, Web Development, Design, Development, Web, TERADATA, UNIX, PROGRAMMER, ORACLE
Production Supervisor with over nineteen years experience in the Biotechnical Industry. Solid background in Bioreactors, Column Chromatography, and Validation. Comprehension of 21CFR, cGMPs, and ISO to ensure FDA compliance. Experienced in training and
I am looking for a position that can use my vast knowledge in Biotech, equipment or Supervisory skills. I also will consider other positions outside the Biotech/Pharmaceutical field. I can work in a team atmosphere or as an individual working on my own projects. I have worked very closely with QA so I believe I could fit in very well with a similiar position. With my supervisor skills I can fit into many leadership role...
Tags for this Online Resume: cGMP, Asceptic Technique, Validation, Manufacturing
Compliant, but flexible...the best of both worlds
I am primarily interested in obtaining a VP position and using my knowledge to truly direct and enhance a companies experience with quality systems and to provide their customers with products that meet or exceed customer expectations.
Ideal Companies: Medical Device Manufacturers
Tags for this Online Resume: Quality Assurance, Project Management, Auditor, ISO 13485:2003, 21 CFR 820, QSR, Regulatory, Management, Medical Devices
looking for a exciting position in pharmaceutical/biotech company
To secure challenging full time position in the field of Pharmaceutics.To work in environment that provides opportunity for learning and growth and to carve a niche in whatever I undertake.
Tags for this Online Resume: Regulatory associate, reseach associate, validation, GXP, CFR, NDA-ANDA
Major strengths include strong leadership, excellent communication skills, competent, strong team player, attention to detail, dutiful respect for compliance in all regulated environment, as well as supervisory skills including hiring, termination, schedu
To obtain a position where I can maximize my multilayer of management skills, quality assurance, program development, training experience, customer service, and a successful track record in the Blood Banking care environment.
Ideal Companies: schools, health, hospital, clubs
Tags for this Online Resume: •Acting Education Manager, American Red Cross, Oakland, CA: 2004 - 2008 •Education Coordinator, CA: 2003 - 2004 •Phlebotomist, CA: 2001- 2003 •Cable Television CATV Supervisor, Core Communication Inc, Sunnyvale, CA: 1998 - 2001 •CATV System Technician, TCI Cablevision Inc, Fremont, CA: 1991 - 1998 •Technician/Day Shift Supervisor, Avantek Inc, Milpitas, CA: 1984 - 1991 •Airport Security Supervisor, Wackenhut, San Jose, CA: 1983 - 1984 •Multi Craft Instructor, APO NY Germany: 1981 - 1983 •Communication Expert, US ARMY, APO NY Germany: 1979 - 1983
Senior Scientist - six years; Associate Scientist II - three years; Bioprocess associate -threr years; Research associate for 5 years; Instructor (HS) - for five years
Experienced senior scientist with expertise in protein or antibody purification. Followed cGMP training with FDA 21CFR part 11 and demonstrated abilities in the scale-up and transfer of purification processes from the laboratory to production. The goal will be using my experience and knowledges for contributions to the biotech industry.
Tags for this Online Resume: Process Development for purification, Monoclonal Antibody purification, GMP Compliance, Large scale design for purification, techniques transfer and disposable technology , team management
environmental compliance specialist
Tags for this Online Resume: DOT 49, CFR 29.1910.120, CFR 40
