Resultados de la búsqueda: 354 vacantes
...project staff.
Needed qualifications:
Leads and / or participates in development, qualification and validation activities for product or technology transfers Cleaning validation, Change Control and Automation experience
Trains production personnel, and other...
...company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to... ...in parental area and equipment validation
• Knowledge of the cleaning process validation, limit determination and equipment trend....
...the requirements established by our customers, to perform and provide a highly effective service.
We are looking for two Cleaning Validation Specialist with Pharmaceutical (solid dosage) manufacturing experience to develop and execute the cleaning validation...
...respect, teamwork, creative talent, enthusiasm and diligence.
General Description:
We are looking for resources to provide Cleaning Validation services in Juncos, Puerto Rico
Essential Duties and Responsibilities:
Development of cleaning revalidation program...
...For Process Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Life Science or Engineering and five years of experience in Validation Life Cycle within the Pharmaceutical Industry.
Bilingual (English...
...Validation Specialist to provide support to qualification and validation activities related to manufacturing equipment. This resource will attend all related meetings, making required documents corrections and changes and following up on document revision and approval...
...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description...
...Mechanical Equipment
System
Equipment Decommissioning
CSV Retirement.
Responsibilities:
~Perform activities related with Validations according to project assignment, customers’ needs and requirements and in compliance with cGMP’s and Safety procedures
~...
...For Validation services in the Engineering and Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s degree in Engineering and a minimum of five (5) years of exposure in Quality activities within the Pharmaceutical or Medical Device Industry...
...For Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Life Science or Engineering and at least Three (3) years of previous exposure in Validation activities within regulated industry.
Excellent reading...
...Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology... ...directly related experience.
~Biotechnology, Validation (Process, Cleaning, etc.), Manufacturing operations.
~Applies extensive...
...Validation Specialist to provide support in manufacturing area and experience in validation laboratory equipment.
Must have experience with:
Laboratory Equipment Validation
Protocols
IQ/OQ/PQ
Documentation
Validation activities.
Requirements...
...Spanish and English
Soft Skills: Communication and Time Management Skills.
Shift: 1 st Shift.
Experience in:
Process Validation Lifecycle (IQ,OQ,PQ,TMV/MSA).
Equipment Troubleshooting
Equiment Validation Protocols (Generation and Execution).
New Product...
$28 - $32 por hora
...OVERVIEW
As a Validation Specialist I, you will be responsible for generating System Development Life Cycle (SDLC) documentation and validating/qualifying systems used in the development and manufacturing of pharmaceutical products. This includes ensuring systems...
...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description...
...Software Validation Engineer with experience in the medical devices industry to validate the software for a new molding machine.
Requirements
~ Bachelor of Sciences in Engineering, Computer Engineering or related field.
~5 years of related experience.
~ Knowledgeable...
...: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.
Essential Functions:
~ The GMP Cleaning and Sanitization Technician is responsible for providing facility/equipment cleaning, and sanitization, in support of GMP manufacturing...
...to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.
The Validation Engineer must have experience with validation projects in Pharmaceutical environment.
Minimum Requirements:
~ Bachelor Degree...
...Validation Specialist with experience in regulated industry to perform chemist laboratory equipment qualifications. Strong knowledge of generation of documents and equipment designs, working with equipment manuals, Data Integrity and Software Validation.
Requirements...
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management...
