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Click Here to search for Good-Documentation-Practice in our 2.4M jobs.
Online Resumes with "Good Documentation Practice"
Professional Administrative & Office Support Assistant
Capable to work under pressure, be a work and detail oriented person who can commit to meet deadlines and goals, also able to establish priorities in an organizational manner.
Ideal Companies: Great Northern Manufacturing, Guess Inc., Jones Plastic Engineering LLC, Krauth Electric, Linak U.S. Inc., Mazak Corporation, NetGain Technology, ORBIS Material Handling, Packstaff LLC, Papercone, Premiere Packaging, Roll Forming Corp, Solectron Global Co. Services, Sonopress LLC, TopWorx Inc., Zeon Chemical L.P. Company
Tags for this Online Resume: Office Support , Clerical, Quality Clerk, Administrative Assistant, Clerk, Document Clerk
Manufacturing/Production Supervisor
Team work,oppertunity to grow-up in the company.All benefits,To learn more in the field.
Ideal Companies: Manufacturing in generic medicine
Tags for this Online Resume: Production Supervisor, Manufacturing Supervisor, Q A Inspector
Manufacturing/Production Supervisor
· Responsible to insure good housekeeping and maintained equipment and rooms in a clean and orderly manner in accordance with cGMP and FDA requirements. · Accurately document as required during all batch manufacturing process paying strict attention to processing step details and good documentation practice. · Responsible for employee performance evaluation. · Maintain the high standard of product quality. · Coordinate ...
QC Associate II
I am interested in working for a leading edge biotechnology company, adhering to GMP and standard operating procedures, good documentation practices, and performing analytical testing. With my skills in HPLC, ELISA, CE-SDS, device testing, cell based assays and wet chemistry, I would make a valuable employee contribution.
Research, 9 years of experience Minneapolis, MN
Tags for this Online Resume: Good Documentation Practice, Good Laboratory Practice, Quality Control, Quality Assurance, Validation, Designated Trainer for new employees
Director of Research
New windows of opportunities to advance clinical research
Ideal Companies: Novartis, Medtronic, Cleaveland Clinic, etc
Tags for this Online Resume: Clinical Research, Electronical Medical Record, Data Management , Clinical research Compliance, Good Clinical practices, Good Documentation Practices, Faculty Healthcare Administration
Validation Documentation Writer, Validation Coordinator, Quality Assurance - 10 years Experience - Indianapolis
To work in a quality-driven environment, such as the biotechnical field, as a Validation Coordinator, Validation Writer, or Quality Assurance Manager.
Ideal Companies: Convance, Clarian, Roche Diagnostics
Tags for this Online Resume: GxP guidelines, Planning Documentation, Regulus, CFR21 Part 11, Testing Documentation, TrackWise, Good Documentation Practices, Microsoft Office
Mexico
Able to expedite the documents required by Latin America BoH. Knowledge of the different sections (CTD) that have direct impact on the product. Knowledge of Latin America regulations relative to pharmaceutical and nutritional products. Capable of preparing documents for registration, variations and product renewals.. Knowledge of Good Documentation Practices. Able to expedite legal documents that make up a dossier. Evaluati...
Chemist - 16 Years of Experience - Near 08016
Result oriented professional with many years of experience in pharmaceutical and consumer health care related industry within a cGMP environment. Worked on various solid, semi-solids, liquid, dosage forms. Performed Method development, Method Validation, Method Verification and Method Transfer. Hands on experience on UPLC (Acvity H-Class), HPLC, GC, Auto-Dissolution USP apparatus I,II and IV(Sotax)Flow through Cell, AA,...
Technician - 20 Years of Experience - Near 53405
• Research and develment Senior Tech with 20+ yrs background with Medical device companies. Quality-focused, with broad knowledge and experience in administrating experimental studies and class B protocols in a research laboratory. • Expertise includes electro-mechanical troubleshooting and repairs, soldering circuit boards, replacing components, and providing technical support to field technicians, nurses and doctors. • S...
Tags for this Online Resume: Medical Device Senior Technician, Laboratory equipment IQ, OQ, PQ and test method validation, FDA and CAPA management, Testing, writing protocols, gauge R , Microsoft Excel, word, outlook, access, and power point, Certified in Blue Hill, , Product development, GLP, GMP, PPE, Engineering Change Request
Chemical Engineer - 5 Years of Experience
Energetic and trilingual quality engineer (member of OIQ) with experience in medical devices, pharmaceuticals and the bottling industry. Offers work experience in a highly regulated (FDA) pharmaceutical environment using Good manufacturing practices (GMP), Good laboratory practices (GLP), Good documentation practices (GDP) as well as Health and Safety issues (CSST). Solid record in designing and validating changes which imp...
Tags for this Online Resume: Los Angeles, Irvine, Quality
Chemist - 20 Years of Experience - Near 33411
I am a Quality Assurance professional with over thirty years of experience in Quality Assurance in the Pharmaceutical, Biotechnology and Medical Device Industry.
Ideal Companies: Medical Device or Pharmaceutical Companies
Tags for this Online Resume: Failure Investigation, Corrective Action, Preventive Action, Training, cGMP's, Florida, Auditing, pharmaceutical
