...equipment , and for Solid Dosage manufacturing equipment .
Solid understanding of Computer Systems Validation for laboratory equipment and for Solid Dosage manufacturing equipment
CSV Life Cycle
Strong Technical Writing Skills...
...Descripcion Independently provides and/or directs the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or manufacturing support environment. Able to troubleshoot systemic...
...Descripcion Under general supervision, provides direct technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing, or manufacturing support environment. Able to troubleshoot basic...
The Validation Specialist/Engineer will be working with the Validation team developing and executing validation activities, protocols, cleaning, sterilization and EBR. The selected candidate must be capable to
Assist in the development, review...
...PROCESS VALIDATION SPECIALIST
Seeking a Senior Process Validation Specialist . Candidate must possess Regulatory Experience in the Pharmaceutical, Biotechnology or Medical Devices industry.
Must possess a solid understanding of...
To provide support in a “ Sanitization Disinfectants Validation Project ”.
~ Bachelor of Sciences.
~5 years of experience in Cleaning Validation field in the Medical Devices industry.
~ Knowledgeable in Cleaning Validation...
...LAB. EQUIPMENT VALIDATION SPECIALIST
This position is open for a Validation Specialist with experience in laboratory equipments in the medical device and pharmaceutical. The candidate must have solid GMP and regulatory experience.
Duties and Responsibilities...
Validation & Engineering Group is currently seeking for a Process Validation Engineer/Scientist to execute and lead process validation activities based on risk assessment effect analysis for pharmaceutical, biotechnology and medical devices industries...
...execution of CSV protocols of Solid Dosage Manufacturing equipment.TECHNICAL COMPETENCIES: Solid understanding of Computer Systems Validation for Solid Dosage Manufacturing equipmentCSV Life CycleStrong Technical Writing skillsExcellent English writing skills...
...generation and execution of CSV protocols of laboratory equipment.
Solid understanding of Computer Systems Validation for laboratory equipment
CSV Life Cycle
Strong Technical Writing Skills
Excellent English writing skill...
...Laboratory Equipment Validation Specialist
Seeking a Laboratory Equipment Validation Specialist WITH EXPERIENCE IN QUALITY CONTROL, QA AND TECHNICAL SUPPORT to perform one or more of the following duties and responsibilities under minimal supervision...
...REQUIRED POSITION QUALIFICATIONS:
The following skills and qualifications are required for this position:
o 18 years of age or over
o A valid driver's license and the ability to meet our driving record requirements
o Possess or are working towards a degree in Business/...
...established in the SLA
• Provide on-call support outside of regular business hours as needed
• Complete special projects as requested; validating functionalities; analyzing existing applications
• Acting as the liaison for new enhancements and products
• Identify repeat...
Follows all safety policies and procedures.
Performs other job-related duties as assigned.
~ Valid Class A or B CDL with air brakes endorsement
~2+ years commercial truck driving experience.
~ Possess a clean safety and driving...
...deploying, training, and supporting users on analytics solutions that meet those requirements. Some other duties include performing data validation to ensure accuracy and appropriateness of the information provided. You will be integral in delivering valuable Information...
...The Quality Oversight Specialist is primarily responsible for the oversight of adjudicated claims (paid and rejected) to validate the accuracy of benefit and formulary set-ups, as well as compliance with laws and regulations. In addition, the Quality Oversight...
HR Shared services: pladis Global and Godiva Chocolatier, In...
...submitted by search firms to any employee at Godiva via-email, the Internet or directly to hiring managers at Godiva in any form without a valid written search agreement in place for that position will be deemed the sole property of Godiva, and no fee will be paid in the event...
...responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve Environmental...
...evaluating alternative workflow solutions
Controls solution by establishing specifications; coordinating production with programmers
Validates results by testing programs
Ensures operation by training client personnel; providing support
Provides reference by writing...
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