...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...
$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...
...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...
...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...
...SUMMARY
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.
FUNCTIONS
- Able to troubleshoot...
...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...
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 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...
...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...
...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...
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...
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...
...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...
...Puerto Rico & USA.
Responsibilities:
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...
...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...
...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...
...SUMMARY
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 knowledge,...
...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.
~...
...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...
...Process Development Scientist with working knowledge of pharmaceutical/biotech processes.
Duties:
Validation and documentation processes in a highly regulated environment.
Operate specialized laboratory equipment and computers as appropriate.
Interpret...
...English & Spanish).
Project Management skills.
Shift: Administrative and according to business needs.
Experience in:
Validation and documentation processes in a highly regulated environment
Vision system technologies
Development and Execution of Processes...
...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....
...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...
...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...
...maintenance a plus.
Supervisory Experience: No supervisory experience.
REQUIRED QUALIFICATIONS
License or Certification: Valid Driver's License
Marriott International is an equal opportunity employer. We believe in hiring a diverse workforce and sustaining...
Marriott International
Rio Grande
2 días atrás
...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 Master's...
...following client requirement/duties for this role;
• Working knowledge of pharmaceutical/biotech processes.
• Familiarity with validation and documentation processes in a highly regulated environment.
• Ability to operate specialized laboratory equipment and...
...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...
...CSV Specialist for laboratory equipment.
Skills:
Laboratory instruments qualification
Validation Cycle
Requirements
Bachelor Degree in Science
At least 5 years of experience in related area
Biligual (Spanish/English)
Technical Writing...