QA Specialist - 35016 - Juncos, PR - Integrated Services For Productivity & Validation, Inc

Nos encontramos en la búsqueda de un/a Quality Specialist para un proyecto en el área Sur de Puerto Rico, dentro de la industria de Medical Devices. · ...

Specialist QA with experience in NPI, Change Control, FAT, Validation and PPQs. · ...

+Job description missing · +Aseptic Process · ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project with one of our key clients. · Develop, review, and execute validation deliverables. · Evaluate systems according to client and regulatory requirements. · ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project.The ideal candidate will have strong experience in validating GxP-regulated systems. · ...

The Specialist QA supports and ensures compliance with quality systems and regulatory requirements in a regulated manufacturing environment.This role is responsible for reviewing and approving quality and manufacturing documentation, · supporting investigations, managing quality ...

The Quality Assurance Specialist provides quality oversight and support for regulated manufacturing operations ensuring compliance with current Good Manufacturing Practices cGMP regulatory requirements and internal quality systems. · ...

· 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 to learn more about our services and solutions · Job Description · Pr ...

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

We are seeking Specialists QA (multiple positions) to work for one of our top biotechnology industry client at Juncos, · PR. · MS degree and 2 years of directly related experience OR BS degree and 4 years of directly related experience (Sciences or Engineering) · ...

The Specialist Manufacturing supports the execution and continuous improvement of manufacturing and quality systems with minimal supervision. · Initiate, revise, review, and approve manufacturing procedures to ensure alignment with current operations; · ,Monitor manufacturing flo ...

Join Amgen's Mission of Serving Patients · At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. · As a member of the Amgen team, you'll help make a lasting impac ...

We are seeking Specialist QA to work in the east region of PR. This job might be an outstanding fit if you have a degree in Life Science or Engineering and experience in QA processes. · Doctorate OR Master degree in Life Science or Engineering + 2 years of directly related experi ...

This Strategic Sourcing Specialist role will be the subject matter expert supporting JLL's sourcing strategies, supplier relationships and program management across both Integrated Facility Management (IFM) and Project Development Services/Small Projects LATAM client portfolio. · ...

+Job summary · Specialist QA with experience in NPI, Change Control, Documentation Review, Validation, PPQ · ,+Qualifications · Doctorate or Masters 2 years of directly related experience or Bachelors 4 years of directly related experience or Associates 8 years of directly relate ...

The candidate will perform one or more of the following duties in support of Amgen's Quality Assurance program under minimal supervision: review product MPs, · approve process validation protocols, · request quality on incident triage team, · and release sanitary utility systems. ...

We are looking for an EHS Specialist to support our Health and Safety initiatives. · ...

+We are united in our responsibility to create healthier futures. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. · + We provide compensation, benefits, and resources that e ...

We are united in our responsibility to create healthier futures, · and every person here is essential to us being able to deliver on that purpose.Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

Support Client's Quality Assurance program under minimal supervision. · ...

The Specialist QA supports and ensures compliance with quality systems and regulatory requirements in a regulated manufacturing environment. · Doctorate degree in Science, Engineering, or related field OR Master's degree with 2 years of directly related experience OR Bachelor's d ...