Resultados de la búsqueda: 254 vacantes
...world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Independently provides and/or directs the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or...
...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...
...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...
...Sr Validation Scientist with experience in Aseptic Process Simulation (Media Fills), Airflow Visualization Studies (Smoke Studies), Environmental Characterization/Qualification. Experience in Parenteral Manufacturing, Isolators.
Requirements
Doctorate degree...
...For Equipment Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and five years of experience in Validation Life Cycle within the Medical Device Industry.
Bilingual (English and Spanish...
...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
~...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level of pharmaceutical support skills under scientific and administrative direction.
Apply sound scientific methods and analysis while...
We are seeking resources with the following expertise;
Experience in Aseptic Process Simulation (Media Fills), Airflow Visualization Studies (Smoke Studies), Environmental Characterization/Qualification
Experience in Parenteral Manufacturing, Isolators
Requirements...
...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 DP Quality Assurance area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s degree in Life Science (preferred in Microbiology) or Engineering with five (5) years of directly experience within the regulated industry.
Bilingual...
$30 - $37 por hora
...This is a contract role for one year
As a Junior Validation Specialist at our pharmaceutical facility, you will be integral in ensuring the compliance and efficiency of our compression and coating processes. Your role will focus on generating System Development...
...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...
...contractors ) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service.
Validation Engineer/Specialist is required to support Validation/Qualification activities in a Medical Devices manufacturing environment....
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...
...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...
...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...
mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services...
Description:
Manages and/or applies extensive technical validation engineering expertise in the coordination of multiple, complex, non-... ...schedules and personnel/fiscal resource utilization and affect the image of the organization’s technological capability. Leads efforts...
...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 process...
...coordinates cost meetings with 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...
