and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com/ to learn... more about our services and solutions! Job Description Validation Engineer to provide support to qualification/validation activities...
in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries... across Puerto Rico and parts of the United States. Its services include the assessment and validation of automation systems, network...
in: Ethylene oxide, steam, liquid chemical, and radiation sterilization methods Process Validation, Equipment IQ, and Computer... software validation knowledge No sterile package design or pharma design The Personality Part: Our Next Piece...
For Equipment Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor... technologies. Systems Qualification & Validation of equipment and utilities qualification, including the ability...
(s): planning, implementation, monitoring, completion, and follow-up. Validation Life Cycle Management The Personality Part..., YOU WILL: (The day-to-day on the job) Define strategy, plan, and coordinate validation activities. Provides guidance on aspects...
validation activities including characterization, OQ, and PQ (non-cleaning), as well as equipment qualification such as URS, FAT..., IQ, OQ, PQ, and TMV (non-laboratory equipment). Experience developing and executing validation strategies, flowing design...
overall quality of the products and minimize validation escapes to customers ESSENTIAL DUTIES AND RESPONSIBILITIES · Create... validation testing schedule, perform tests and report test results to ensure that they meet hardware design specification...
). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert... & Cleaning Specialist (SME): CIP and SIP processes GMP Document Controller: Validation Protocols (IQ/OQ/PQ), Risk Assessments...
For Process Validation services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor...'s in Engineering with five (5) years of experience in Process Validation activities within the Pharmaceutical Industry. Excellent...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...] (not laboratory). Experience in production line. Basic knowledge in defining validation strategies (e.g. requirements flow down...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...] (not laboratory). Experience in production line. Basic knowledge in defining validation strategies (e.g. requirements flow down...
For Process Validation services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor...'s in Life Science or Engineering with five (5) years of experience in Process Validation activities within the Pharmaceutical...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...] (not laboratory). Experience in production line. Basic knowledge in defining validation strategies (e.g. requirements flow down...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...] (not laboratory). Experience in production line. Basic knowledge in defining validation strategies (e.g. requirements flow down...
For Validation services in the Global Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor... on the job) Generate and execute comprehensive facility and utility validation protocols Oversee validation processes...
For Validation services in the Manufacturing areas. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree... in Engineering and at least four (4) years of exposure to Validation Engineering activities within the Pharmaceutical or Medical...
Validation Specialist — Equipment Location: Barceloneta, Puerto Rico (On-site) Shift: Day (7:00 a.m. – 5:00 p.m....) Start: ASAP Role Overview Execute and support validation for new and existing equipment, partnering closely...
). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert... & Cleaning Specialist (SME): CIP and SIP processes GMP Document Controller: Validation Protocols (IQ/OQ/PQ), Risk Assessments...
. Minimum of 4 years of relevant experience in quality or manufacturing engineering with process and CSV validation...
Date Posted: Country: United States of America Location: US-PR-AGUADILLA-110 ~ Rd 110 N Km 28.8 ~ RD110 Position Role Type: Hybrid U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required...