Resultados de la búsqueda: 6 vacantes
...committed to work under the highest ethics standards for the following position:
~Documentation Specialist for GMP Industry
Qualifications:
The Documentation Specialist will work with the Document Control Group Leader to achieve an efficient operation of the Document...
...and submit permit applications, including gathering necessary documentation and completing required forms.
~Communicate with regulatory... ...and as part of a team in a fast-paced environment.
~Proficiency in Microsoft Office suite and other relevant software/tools....
...experience in configuring computerized systems with complex vendor software systems, and windows operating systems.
Must have... ...backup, restore, etc.
Knowledge of cGMP, GXP, GAMP, and good documentation practices.
Advanced knowledge of pharmaceutical, manufacturing...
...Works with the Sites’s IT Computer System Validation Manager (or designee) and the site’s areas in development and execution of software/computer validation plans for automated equipment, processes, and systems.
Identifies computerized systems validation needs through...
...QA/CSV Consultant with experience in Electronic Record Software and quality regulations review.
Software Validations knowledge
Strong knowledge of Electronic Record Review
Quality Systems
Requirements
Bachelors Degree and 5 years of experience...
...Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
Essential Functions:
Asset/system decommissioning and documentation lifecycle closeout.
Asset Decommissioning
Mechanical Equipment
System
Equipment Decommissioning
CSV Retirement....
