Resultados de la búsqueda: 150 vacantes
...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...
...company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to... ...knowledge of GMP regulations and guidelines.
• Knowledge of the cleaning process validation, limit determination and equipment trend....
...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...
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...
$32 - $45 por hora
...OVERVIEW
As a Validation Specialist II, 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...
...For Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s degree in Life Science with five (5) years of validation expertise experience within the regulated industry.
Bilingual (English & Spanish)
Project...
...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...
...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...
...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...
...ingenuity and creativity.
2. 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.
3....
Description:
Manages and/or applies extensive technical validation engineering expertise in the coordination of multiple, complex, non... .... Expert validation knowledge (equipment qualification, cleaning, sterilization). Is recognized as a leader and authority in company...
...Validation Specialist with esperience in regulated industry. Knowledger with manufacturing equipment, laboratory equipment and facilities.
Tasks:
Execute complete validation cycle
Change Control
Equipment qualification (manufacturing and laboratory)...
...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 & 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...
...various ""Housekeeping"" activities, (i.e., keeping work areas clean, cleaning of equipment etc.)
All work must be completed in accordance... ...HVAC P&ID’s.
Assist with the development and execution of validation documents for mechanical equipment.
Demonstrate expertise in...
...various ""Housekeeping"" activities, (i.e., keeping work areas clean, cleaning of equipment etc.).
4. Ensure that operational log... ...specifications.
14. Assist with the development and execution of validation documents for mechanical equipment.
15. May have led...
...before they occur.
Ensure completion of regular maintenance and cleaning projects on a biannual basis.
Monitor all V.I.P.'s, special... ...approved spreadsheets and word processing.
Must have a valid driver’s license of Puerto Rico.
Must be able to convey information...
...process development, utilities, facilities, quality assurance and validation departments in developing recommendations for large and/or... ...Cell Culture, Protein Purification, Media and Buffer Preparation, Clean Utilities, CIP, SIP and Production Services. 3. Direct...
...instrumentation/calibration/electrical systems, and technical cleaning systems are maintained in compliance with all applicable industry... ..., microbial/environmental issues, technical cleaning issues, validation issues, electrical issues, and process maintenance issues.
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