jt890 - associate quality applications specialist - Juncos

The Associate Quality Application Specialist supports the validation, administration, · and compliance of quality-related computerized systems in a regulated environment. · ...

We are seeking an Associate Quality Application Specialist who will conduct compliant validation processes for quality information technology systems. · ...

· ,Bachelor's Degree in Life Sciences or Engineering and previous exposure within the Pharmaceutical & Medical Devices Industry. · , Spanish and English · , Excellent Communication skills · , Six Sigma, CAPA, · SAP QM Module.,TrackWise Systems ,Agile System · & FactoryWorks Syst ...

We are a Service Provider company different from the rest. We integrate Engineering Construction Maintenance Utilities and Specialized Technical services across the Island (and in the US as well). · ...

A leader in the pharmaceutical industry is looking for a motivated and enthusiastic team member to join their team. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · Specialist Tech Engineering · The Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strate ...

We are seeking a talented individual committed to work under the highest ethics standards for the following position: Quality Assurance Specialist.The QA Specialist plays a critical role in ensuring that all biotechnology and pharmaceutical products meet regulatory standards and ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Validation Specialist. · ...

Job summary:This is a manufacturing engineer position at Quality Consulting Group in Puerto Rico & USA. The successful candidate will work with a highly enthusiastic team contributing to the world-class manufacturing industry. · Responsibilities :Assesses impact of IT reports/app ...

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. · ...

We are seeking a talented Quality Professional with Manufacturing Process Audit experience. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

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) · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Specialist QA. · ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g. ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities ensures the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g., WFI, RO/DI), clean ...

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. · ...

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 ...

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 ...

Provides characterization of process optimization strategies and/or troubleshooting of operational issues in operations, manufacturing, pilot plant environment. · ...

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 ...