...empresa
Sika MBCC , es una empresa especializada en productos químicos líder en el desarrollo y producción de sistemas y productos... ...la entrega del servicio/producto.
- Controlar, recibir y validar las facturas de los acarreadores registrandolas en SAP como costos...
...Validation Specialist to perform activities related to qualification of laboratory equipment in a Medical Devices industry.
Requirements
~ Bachelor Degree
~3-5 years of experience
~ Knowledge and experience in a GMP regulated environment
~ Bilingual: English...
...Validation Specialist with experience in regulated industry, validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities.
Tasks:
Execute complete validation cycle
Change Control
Equipment qualification (manufacturing...
...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...
...For Validation services in the Packaging area
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree with five (5) years of experience within the pharmaceutical or medical device industry.
Bilingual (English & Spanish).
Project Management skills...
...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...
...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...
...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...
...enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating...
...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...
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...
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...
...Biotech®, it’s about more than just a job—it’s about your career and your future.
Your Role
This is an open application for Validation Engineers in the life science industry. We look forward to learning more about your experience, expertise, and career goals and...
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...
...colocar el número de referencia en el espacio provisto en la solicitud. Requisitos:• Área de Cayey• Bachillerato completado en Ciencias (Química, Bioquímica, Microbiología, Biología o Ingeniería)• Mínimo 1 año de experiencia en calidad en ambiente medical device o...
...understanding of the client and the property intended to finance. Understands the requirements and conditions of each mortgage product, validates each aspect of the application in order to sustain an effective evaluation. Contacts the client to guide, clarify doubts and...
...troubleshooting mentorship.
Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications.
Support the execution of...
...partially completed and completed work for compliance with FEMA requirements.
Documenting and advising stakeholders on the technical validity of claims.
Identify feasible hazard mitigation strategies that comply with all programmatic and regulatory requirements and...
...Review equipment/system Root Cause Analysis investigations and support trend evaluation.
Assist with generation of process validation protocols and reports.
May participate in regulatory inspections
Participate in the NPI process to assess requirements for...
...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...
...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...
...engagement requests for quality purposes and provide assistance as needed to ensure risks are adequately analyzed and addressed.
• Validate and confirm the subject matter experts within Popular that need to participate in the risk assessment and due diligence process....
...feature backlog.
The Business Analyst is responsible for the integrity of the requirements from beginning to end. The redaction and validation of the user stories and the definition of done in each sprint; uses modeling tools to document the current state of business...
...Engagement: Collaborate with stakeholders, including customers, end-users, business leaders, and development teams, to gather and validate requirements. Act as the primary point of contact between stakeholders and the development team, ensuring clear communication and...
...Minute Accounting metrics includes properly tracking AW status and research data anomalies across multiple systems, generate and validate Minute Accounting data reports, collaborate with teams on data setup and possible new requirements across systems as needed.
Assist...
...and/or changes to existing process. Lead and/or participate in related meetings. Act as the Unit Representative in meetings.
• Validate the correct accounting procedures are in place based on Popular Accounting Guidelines.
• Review and update processes to identify...
...equipment to ensure it meets all instrumentation design specifications.
Assist with the development and lead in the execution of validation documents for instrumentation equipment.
WHO WE ARE:
We are a Service Provider company different from the rest. We pride...
...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...