Resultados de la búsqueda: 100 vacantes
...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...
...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...
...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 & 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...
$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...
...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...
...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...
...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...
...Nonconformance Reports
Execute and/or approval Manufacturing and Quality System procedure changes
Execute and/or approval of Process Validations and Qualifications
Develops, modifies, applies and maintains quality standards and protocol for processing materials into...
Description:
Manages and/or applies extensive technical validation engineering expertise in the coordination of multiple, complex, non-routine projects involving the planning, design, reconfiguration, construction, maintenance and alteration of processes, systems or...
...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
Create...
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...
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...
...Description:
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance...
...regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues, and process maintenance issues.
~ Assist the maintenance team during FDA and other regulatory agency...
...ingenuity and creativity.
Work with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/or highly complex system/facility modifications.
Work...
...multiple organizational units.
~ Work with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/or highly complex system/facility modifications.
~...
...pharma industry.
Experience and knowledge in:
Packing Equipment
Design of New Equipment Process
Engineering Project
Validations and Commissioning
CAPA and Compliance
Availability for 1st or 2nd shift
Requirements
Doctorate degree or Masters...
...manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise; including but not limited to Deviation’s, CAPAs, and validations
• Actively engage in Continues Improvement initiatives, programs and projects
• Vigilant ensuring that changes that could...
