VALIDATION INTERNSHIP IN PUERTO RICO FOR
RECENT PROFESSIONALS
NEWLY GRADUATES
STUDENTS
Start your career with a VALIDATION Internship in Puerto Rico
Why a VALIDATION Internship IN PUERTO RICO ?
The purpose of the CIQA internship in Puerto Rico is to boost the careers and jobs, for new professionals in the aftermaths of Hurricane Maria and the Earthquake(s).
This internship is designed to bring a valued process excellent education and on-the-job experience to new hire professionals, even students in their last semester.
Initially, it consists of intensive classes and education remotely or in the CIQA Learning Center. Finally, it includes a workshop with practice in a working experience with coaching in the pharmaceutical industry, medical devices or health IT information technology field.
What makes this validation internship unique?
It extends the academic background in the most demand areas within the regulated life sciences industries. This initiative develops the careers in Puerto Rico of talented prospects with the technical basic needs of the regulated Life Sciences Industries.
The CIQA learning center was developed based on client requirements and in compliance with industry standards.
We have multiple jobs in Puerto Rico available that allow you to be trained and work anywhere, including from your own home.
We offer a comprehensive benefits package, if you complete this Internship in Puerto Rico and get selected for a regular job employment. It includes health insurance, vacations, sick days, holidays, recruitment fee, referral fee and much more.
IF you want a validation internship in Puerto Rico.
Information you may need to know.
Who can apply?
Any prospect engineer, software developer or scientist interested in learn and grow in the FDA regulated industry may apply for an CIQA internship in Puerto Rico. To benefit from it, you must:
- Be graduated or in your last semester before graduation
- Be on assignment for minimum 12 months
- Meets performance expectations
- Engineering, science, computer degree
- Bilingual (English and Spanish)
- Professional and personal growth desire
What do you get?
Our goal is that such training and education will translate into new careers in Puerto Rico. As part of the CIQA internship in Puerto Rico, you can receive:
- Per-Diem-Diet Reimbursement
- Recruitment, Productivity and Withholding Bonus
- CIQA Apartment Acommodation
- Referral/Sales Bonus
- Work Place Bonus
- Social Responsability
- Networking Forums
- CIQA Academy Training
- Access to CIQA Library
What kind of projects will I be working on?
CIQA Internships in Puerto Rico support a broad range of projects and services. It will on the depends on the needs of our clients.
Typical projects depends of your areas of interest and education:
- Validation Engineering
- Manufacturing Engineering
- Quality Engineering
- Process Excellence Engineering
- Software Design & Development
- Social Media Marketing
Where will I be located?
During the CIQA Intership, you will be working remotely or located at the CIQA Learning Center in Hormigueros, Puerto Rico for several weeks.
After finishing the initial training, you will be working remotely or located in one of our projects locations jobs in Puerto Rico or US during approximately at least 8 weeks. You will have your own couch and working area with internet connection and access to our library of training, templates, procedures, courses and standards. For additional information you can contact us at email: company@ciqa.net
CIQA offers a variety of technical interships depending of your needs to fulfill the industry requirements and professional career. Our instructors will evaluate your profile and provide you with a custom training just for your needs. Our instructors will evaluate your profile and provide you with a custom training for intersnships in Puerto Rico, such as:
- Change Control Management, ICH Q10 -
- Document Control Management DCM
- CAPA Corrective and Preventive Actions
- Calibration and Preventive Maintenance Management
- Facilities and Utilities Qualification
- CSV Computer System Validation
- Cleanroom Qualification ECA
- Installation, Operational and Performance Qualification
- Process Excellence, Lean Manufacturing, 5S & 6 Sigma
- Cleaning Validation
- ISO 13485 - Medical Devices-Quality Management
- Project Management and Risk Management
- Quality Management System (QMS) - GMP Good Manufacturing Practice
- Conversational and Technical Writing Training
