effective service. The Validation Engineer will support Validation/Qualification activities in a Medical Devices manufacturing... and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, - Requirements...
(8) years of experience as a C&Q Engineer within the pharmaceutical or regulated industry. Bilingual (English & Spanish...). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert...
(8) years of experience as a C&Q Engineer within the pharmaceutical or regulated industry. Bilingual (English & Spanish...). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert...
Job Title: Quality Engineer - Validations Experience a must Position Summary: We are looking for a skilled... and driven Quality Engineer to develop, implement, and maintain quality standards and procedures across the manufacturing process...
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...
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...
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 Sterile and Filling area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor...: Administrative, and flexible to business needs. Due to validation activities, support must be available for 1st, 2nd, and 3rd...
JOB DESCRIPTION Responsibilities may include the following and other duties may be assigned. Provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to m...
JOB DESCRIPTION Responsibilities may include the following and other duties may be assigned. Provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to m...
Position Summary: We are looking for a skilled and driven Quality Engineer / Process Engineer to develop, implement... in quality or manufacturing engineering with process and CSV validation; or an advanced degree with equivalent experience...
Job Description: Under general supervision, the Manufacturing/Process Engineer provides technical support for process..., and validation) to develop system modifications. Assist project managers with design, engineering, and construction projects...
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 Engineer with experience in regulated industry to provide technical engineering...
Process Engineer I requires: Availability to work extended shifts (8- 12 hours per shift) Availability to work... shift (If require) mainly first shift Minimum 2 years in experience in Process Validation and / Computer System...
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...
mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation... United States. Its services include the assessment and validation of automation equipment, network infrastructures...
) 2+ years in experience in Process Validation and / Computer System Validations Knowledge in Medical Devices... regulations Experience working and executing Design transfer activities Basic knowledge in defining validation strategies (e.g...
) 2+ years in experience in Process Validation and / Computer System Validations Knowledge in Medical Devices... regulations Experience working and executing Design transfer activities Basic knowledge in defining validation strategies (e.g...