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Online Resumes with "cgmp "
Statistician with extensive experience in developing innovative solutions
Extensive experience in the pharmaceutical, aerospace and financial services industries. Expertise in statistical analysis: Statistical Process Control (SPC); in the design and analysis of experimental plans and monitoring of test results to improve manufacturing processes and quality assurance. Demonstrated ability in building ad-hoc queries from production, financial, staffing and competitor market research databases. Str...
Tags for this Online Resume: Training, Regression Analysis, Statistical Process Control (SPC), JMP, Minitab, SAS, Technical Writing, Lean Kanban, Geometric Dimensioning (GDT), Six Sigma, Design of Experiments (DOE), Multi-Functional Team Leadership, Lean Manufacturing including 5S
Biological Technician - 6 Years of Experience - Near 27513
My qualifications include my Bachelor's in Biology. Also of note is my most recent position as an Associate Bio-Processioning Technician for Merck and Company. In this role, I am responsible for performing various operational tasks as part of an empowered team. I currently work in a cGMP environment, while operating and monitoring equipment. I attend safety training and compliance events on a regular basis, and I routinely...
Tags for this Online Resume: Technician , Chemist, HPLC, FDA, CAPA, Anaytical
Biological Technician - 12 Years of Experience - Near 33601
Manufacturing Sr Associate with 12 years of experience in the biotechnology industry. Knowledgeable in areas such as: Lean process, (Yellow Belt Certification), Quality Process, cGMP, Standard Operating Procedures (SOP’s), Operator of Inova. Bausch & Ströbel and TL vial fillers equipment, environmental monitoring, gowning and aseptic techniques. Capable to work efficiently on group with leadership to take decisions. Abili...
Tags for this Online Resume: biotechnology, Manufacturing , pharmaceutical, parenteral, steril, filling, spanish, lean
Quality Assurance Director - 20 Years of Experience - Near 19086
I am an experienced professional scientist with over 25 years of Research and Product Development and cGMP manufacturing experience in the pharmaceutical and biotechnology industries. I have a proven track record of directing and delivering high profile multi-million dollar projects and contracts on time or ahead of schedule and meeting exacting specifications (purity, potency and quantity of purified biologics).
Tags for this Online Resume: Philadelphia, PA, Process Development, Monoclonal manufacturing, Viral removal technology, Viral Vectopr Manufactrunig, Upstream Bioreactor Process, Downstream Chromatographic Purification
Auditor - 19 Years of Experience - Near 11224
Cover Letter Ignace Vallejo, MS. Sr QA Compliance Specialist. Certified Quality Auditor GMP; by CFPA. 525 Neptune Ave, Brooklyn, NY 11224. Apt 22 F Home # 718 946 0556. Mobile # 917 359 3028. ignaciovallejo@optonline.net To whom it may concern: I am applying for the position of Mgr and Regulatory Compliance. I have 19 years of experience working in the Pharmaceutical Industry. My experienc...
Ideal Companies: Large company
Tags for this Online Resume: QA, QC, Scientist, Auditor, Medical Liaison
Director of Global Real Estate and Facilities - 20 Years of Experience - Near 45243
To obtain a senior management position using established skills in management, operations, construction management, facilities, maintenance, calibration, cGMP design, project implementation and staff development.
Tags for this Online Resume: Facilities, Pharmaceutical, Engineering, Maintenance, Calibration, Validation, CMMS / BAS, Management
What I know is not taught in college.
Given the experience I have I can be of tremendous value and hit the ground running making a substantial impact in just a few months once I learn and understand your systems.
Ideal Companies: Pfizer, Johnson & Johnson, Idec, Lilly, Custom Processing Services, Waste Management
Tags for this Online Resume: Project Manager, Six Sigma, Team Building, Master Scheduler, Training, Mentor
Manager - 20 Years of Experience - Near 19038
Project Management | Procurement Management |Quality Assurance Project Management: Successful Project Manager with 10+ years of experience in the pharmaceutical industry commercializing over-the-counter new products and line extensions. Proven career record of producing multi-million dollar profits through the leadership of cross-functional teams and strategic identification and implementation of cost savings and effective...
Tags for this Online Resume: Project Manager, Philadelphia, Administrator, Analyst, Purchasing, Operations, Pharmaceutical, Self motivated
Quality and Operations Excellence Professional
An opportunity to create long term sustainable value for a company through facilitating a culture of risk management and process optimization
Tags for this Online Resume: Quality, Operations Excellence, Compliance, ISO, CGMP, Product Stewardship, Quality engineer, Auditor, Process Management
Validation Consultant-18 years experience in cGMP regulated environment-Dallas, Georgia
Technically accomplished, results oriented professional with 17 years CFR Part 11and GAMP 5, Part 58, Parts 210 & 211, Part 600, 601,610, Part 1270, 1271and Part 820 cGMP regulated environment with 10 years working experience writing, developing and executing validation protocols, managing calibration programs, maintaining and upgrading automated systems in a cGMP environment. Creative Metrologist/Chemist/Biologist and (IQ,...
Process Scientist - Southeastern PA - 25 years cGMP experience - 13+ years in Biopharm
To secure a position in a cGMP regulated Pharmaceutical or Biopharmaceutical environment in which my years of relevant experience can be utilized. Positions related to "Process Scientist", "Scientist", "Engineering", "Process Equipment/Instrument/Biopharm Sales" ALSO to be considered.
Tags for this Online Resume: Aseptic technique, Technical support, GMP, monoclonal antibody, Project, Process
Clinical Quality Assurance - 20 Years of Experience - Near 94403
QA/QC experience working with FDA ICH and Japanese regulations 21 CFR reviewing Writing editing submission documentation SOPs Protocols Reports. Product/Project analytical requirements evaluation budget in-house vs. out-source estimation. Upgrading of R&D laboratories to GLP/GMP level.
Ideal Companies: small start-up company
Tags for this Online Resume: methods transfer validation, phase I, II, III protocols and reports, GMP GLP, Laboratory management, hiring training budgeting, FDA ICH regulations, validation monitoring transfer, medical devices, Consulting, Document Review, Documentation, DSC, High Performance Liquid Chromatography (HPLC)
