LL02-251008 TOP Documentation Specialist - Juncos

We are seeking a talented Calibration Documentation & Planning Specialist to support calibration planning and documentation activities. · Key Responsibilities · Support calibration planning activities for a group. · Perform documentation review and management for calibrations exe ...

We are seeking a Computer System Validation (CSV) Specialist with more than five years of experience in the biotech industry to support validation activities for regulated computerized systems. · Support planning, execution, and documentation of computer system validation activit ...

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 ...

We are seeking a talented individual committed to working under high ethics standards for the position of CQV Specialist. · The ideal candidate will have prior experience with biotech processes, familiarity with regulatory standards (FDA/EU Annex 15), and ability to work cross-fu ...

The Commissioning and Qualification (C&Q) Specialist for Process Equipment will lead and execute the commissioning and qualification activities for syringe filling lines in a regulated GMP environment. · The role requires expertise in process equipment validation, · including fil ...

The Commissioning and Qualification (C&Q) Specialist for Laboratory Systems in QC is responsible for ensuring the successful implementation, validation, and qualification of laboratory systems used in Quality Control environments. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Specialist - Smoke Testing / Airflow Visualization. · Plan and execute smoke studies (airflow visualization) for cleanrooms, RABS, isolators, filli ...

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 ...

This role involves working with a highly enthusiastic team in a world-class manufacturing industry in Puerto Rico & USA. · Responsibilities: · Execute equipment & test method validations · , reviews the work of other specialists; may manage some elements of projects. · ...

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're seeking a Specialist QA to work for one of our top Biotechnology Industry clients at Juncos, PR. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

We are seeking a talented, · d · dicated individual committed to work under the highest ethics standards for the following position: · QA SpecialistThe QA Specialist ensures compliance with quality systems,overses batch record reviews,and supports the implementation of new produc ...

The Senior Engineering Specialist independently leads process optimization,troubleshooting,and engineering initiatives within manufacturing,pilot plant,operational or capital project environments. · ...

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 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 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. · ...

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

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Specialist Quality Control. · Under general direction, functions as the technical specialist for testing and development in areas of molecular biology ...