LL01-062025 Validation Specialist for Biotech and Aseptic Process - Juncos,

Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically, experience focused on Aseptic Process Validation, Aseptic Techniques, Environmental Monitoring Performance Qualifications, Environmental Characterizations, Airflow Visualization (Smoke Tests). Expe ...

mîrus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of th ...

Specialist QA with experience in Aseptic Process FAT's Validation PPQ's NPI Change Control. · ...

Sr engineer with experience in design experiments and aseptic manufacturing. · ...

For validation services in the sterile and filling area. · Bachelor's Degree in Life Science or Engineering and a minimum of five (5) years of experience in the regulated industry. · Excellent written and verbal skills in both English and Spanish. · ...

Company Description · 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 http://www./ to learn more about our services and solutions · Job Descrip ...

This job involves working as a Specialist QA with experience in Aseptic Process NPI Change Control FAT's Validation PPQ's. · Bachelor’s + 4 years of directly related experience or Associate + 8 years of directly related experience Bilingual (Spanish/English) · ...

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you'll work with a highly enthusiastic team, contributing in a world-class ...

Sr Engineer with experience in regulated environments and ability to apply GMP in manufacturing and validation. · Doctorate or Masters + 2 years of Engineering experience or Bachelor's in engineering + 4 years of Engineering experience. · Bilingual (Spanish/English)(Write/Speak) ...

For Validation Services in the Quality Assurance area. · WHAT MAKES YOU A FIT:  · The Technical Part: · Bachelor's Degree with four (4) years of experience in a Scientist within the pharmaceutical or regulated industry. · Bilingual (English & Spanish). · Project Management skills ...

+Quality Consulting Group is looking for a talented specialist QA to join their team in Puerto Rico & USA. · +Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

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The Senior Engineer will provide advanced technical leadership to support manufacturing operations, · process optimization, technology transfer, and continuous improvement initiatives within a highly regulated pharmaceutical environment.Lead and execute complex engineering assess ...

+Review and approve product MPs Approve process validation protocols and reports for manufacturing processes Request Quality on incident triage team Approve Environmental Characterization reports Release of sanitary utility systems Approve planned incidents Represent QA on NPI te ...

Quality Consulting Group, is looking for a talented and enthusiastic specialist to join their team in Puerto Rico & USA. · ...

+We are looking for a talented and motivated Senior Engineer to join our team. In this role, you will work with a highly enthusiastic team in the manufacturing industry in Puerto Rico & USA. · +Provides characterization of process optimization strategies and/or troubleshooting of ...

Quality Consulting Group is looking for a specialist QA to join their team in Puerto Rico & USA. · Review manufacturing process documentation and GMP documents. · Approve protocols and reports. · Participate in incident triage teams and review planned incidents. · ...

+Job summary · Quality Consulting Group is looking for a talented QA specialist to join their team in Puerto Rico & USA. · +ResponsibilitiesReview, approve, and maintain manufacturing process documentation (MPs) in compliance with cGMP requirements · ...

We are looking for a talented, highly motivated and enthusiastic Quality Consultant to join our team. In this role, you'll work with a highly enthusiastic team contributing in a world-class manufacturing industry in Puerto Rico & USA. · Review, approve, and maintain manufacturing ...

We are seeking for talented dedicated individuals who are committed to work under the highest standards of ethics to and with expertise in the following area Process Development Scientist. · ...