...international regulations which govern the user's applications.
Reports on the status of validation... ...experience
Experience as Quality Specialist in medical devices of pharmaceutical... ...with rigor and provide guidance where applicable
Support development, review and...
...within the company and airlines. Handles the installation and configuration of the software and hardware, operating systems and applications for users within the company. Administers all the equipment repairs.
Salario $14.00
Información adicional
“Patrono con...
For Engineering support services in the Quality area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and four (4) years of exposure within the Pharmaceutical & Medical Devices Industry.
Bilingual: Spanish and English
Soft Skills...
...Job Type
Full Time Opportunity
General Description
Conducts audits of data processing systems and applications to safeguard assets, ensure accuracy of data, and promote operational efficiency.
Essential Duties and Responsibilities
Performs interviews and...
...conformance with cGMP’s plant procedures, corporate policies, and applicable regulations (FDA, ENEA, DEA, etc.)
Prioritizes projects and... ...YOU WILL: (The day-to-day on the job)
Works with the Sites’s IT Computer System Validation Manager (or designee) and the site’s...
...and distributed to the highest standards, in compliance with all applicable regulatory requirements.
Our goal is to skyrocket our... ...tools that will help you grow and learn.
At PSC Biotech®, it’s about more than just a job—it’s about your career and your future...
...Investigations Specialist with experience in regulated industries. Strong knowledge of complaints and processes deviations. Will be responsible... ...:
Understanding of the investigation process as it applies to manufacturing issues and complaints.
Understanding...
...mientras haya una relación de trabajo. Patrono usuario de E-Verify.Requisitos:REQUISITOS: -BACHILLERATO EN SISTEMAS DE INFORMACION (IT) -EXPERIENCIA PREVIA EN LA PROFESION DE IT -EXCELENTES DESTREZAS EN SISTEMAS COMPUTARIZADOS -EXPERIENCIA EN SOFTWARE, HARDWARE Y TROUBLESHOOTING...
...administration of customer contract reviews as it pertains to quality and compliance... ...improving our performance. Compliance Specialist 2018 2 Job Description GIDEP).
Act as... ...skills
~ Computer literacy with MS Office applications
Physical Requirements and Working...
...initiates corrective action of problems and deficiencies to ensure product quality.
Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.
Ensures processes and procedures are in compliance with regulations...
...area, client outreach, and appointment scheduling. In this role, it is important that you quickly and expertly assess the needs of... ...goals and objectives.
Conduct orientation and interview with applicants including parent in case of minors.
Perform applicant files procedures...
...implementation of the Quality and Compliance program for a state-of-the-art pharmaceutical/ medical device manufacturing facility as it relates to the facilities maintenance of this plant.
~ Report on critical & key performance measurements. Submit periodic task reports...
...BR IT Synergy LLC (Synergy) is the technology arm of one of the largest conglomerates in Puerto Rico. It was created in 2009 with... ...organization and assist non-IT users who are having computer or application problems.
Test and evaluate existing network systems....
...organizations across the Island and parts of the United States. Its services include the assessment and validation of automation... ...Strong word processing, presentation, database and spreadsheet application skills.
Strong communication (both written and oral), facilitation...
...live and connect with what matters most, wherever you are, doing it better than any other company.
What's the role?
The... ...Team, your role will focus on security architecture, securing applications, networks, services and information, compliance and remediation...
...growth and success from each and every one of its employees?
If so, AIDS Healthcare... ...INTERESTED? Please continue !
A Patient Care Specialist 2 (PCS2) contributes to AHF by embodying... ...initiatives.
To be successful as a PCS2 it is crucial to ensure that the AHF Core...
Minimum Requirements
Mid-level individual contributor on a project or work team, 3-5 years of experience required.
Bachelor Degree in Engineering
Experience within Medical Devices and/or Pharmaceutical industries.
Experience in equipment IQ, OQ and PQ, Validation...
...handling of documents from the ground up
Oversee document through its entire lifecycle (inception to archival)
Check and edit... ...commitment to maintaining a safe and productive work environment, all applicants for employment with our company are required to affirm their...
For Equipment Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and five years of experience in Validation Life Cycle within the Medical Device Industry.
Bilingual (English and Spanish)...
...for businesses.
The Cybersecurity Risk & Incident Response Specialist is responsible for the information security analysis, incident... ...related to the installation of unregistered software by analyzing its vulnerabilities and risks.
Execute all key controls...
...ofrecer apoyo a todos los asociados de la empresa
Verificar la funcionalidad de los componentes ¨software¨ ¨hardware¨ y herramientas de IT.
Monitoriar el cumplimiento de políticas, procedimiento y controles internos para las actividades de administración de los sistema...
...to verify their efficiency, and investigates and initiates corrective actions.
Complies with company programs, procedures and applicable quality system regulations and standards.
Leverages technical expertise and knowledge of standard engineering approaches, design...
...evaluate compliance issues.
• Microsoft Office spreadsheet and application skills and presentation knowledge.
• Strong communication (... ...in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law....
...pharmaceutical products are manufactured, tested, and stored, according to current Good Manufacturing Practices (cGMP) and other applicable regulations. • Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices...
...Product Introduction
Administrative Shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,,...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
QA Specialist to make reports to determine if the stabilities are going to be included in a reduced testing program. Must be fully bilingual (...
...Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
Validation Specialist to provide support to qualification and validation activities related to manufacturing equipment. This resource will attend all related...
...ready to take on this new challenge?
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
Inspects projects area to ensure it is a hazard-free environment.
Equipment safety assessment.
Environmental assessment.
Reviews and approves all subcontractor’...
...what matters most, wherever you are, doing it better than any other company.
What's the role?
As a Provisioning Specialist you will works with a team of skilled SMEs... ...deployment teams during the transition of applications into production
Validate application performance...
...at all levels.
Availability for 1st shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,,...