Autoclave Performance Qualification Specialist - Juncos
hace 2 semanas

Descripción del trabajo
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Accede a todos los puestos de alto nivel y consigue el trabajo de tus sueños.
Trabajos similares
As Commissioning & Qualification Specialist at Mentor Technical Group (MTG), you will collaborate with C&Q Engineers to develop commissioning and qualification procedures. · Collaborate with C&Q Engineers to develop and maintain commissioning and qualification procedures and docu ...
hace 1 mes
For Commissioning and Qualification services in the Capital Projects area. · ...
hace 1 semana
LL01-122024 Validation Specialist – Laboratory Systems (QC)
Solo para miembros registrados
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. · ...
hace 1 mes
LL02-122024 Validation Specialist – Process Equipment (Syringe Filling Lines)
Solo para miembros registrados
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 ...
hace 1 mes
LL03 - 122024 Validation Specialist– Utilities and Facilities
Solo para miembros registrados
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 ...
hace 1 mes
Validation Specialist (Facilities & Utilities) LL01-250822
Solo para miembros registrados
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. ...
hace 1 mes
LL02-251114 - CQV Specialist – Smoke Testing / Airflow Visualization
Solo para miembros registrados
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 ...
hace 1 mes
LL01-260108 Calibration Documentation & Planning Specialist
Solo para miembros registrados
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 ...
hace 1 mes
Validation Specialist (Upstream Process Equipment) LL04-250822
Solo para miembros registrados
CQV Specialist for Upstream Process Equipment. · The CQV Specialist for Upstream Process Equipment will be responsible for the commissioning and qualification of systems supporting cell culture operations in a cGMP biotechnology manufacturing environment. · Bachelor's degree in e ...
hace 1 mes
Validation Specialist (Downstream Process Equipment) LL03-250822
Solo para miembros registrados
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 ...
hace 1 mes
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 ...
hace 1 semana
+Job description missing · +Aseptic Process · ...
hace 6 días
Specialist QA with experience in NPI, Change Control, FAT, Validation and PPQs. · ...
hace 1 mes
MV05-020526 Computer System Validation (CSV) Specialist
Solo para miembros registrados
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 ...
hace 2 semanas
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 ...
hace 1 mes
LL01-062025 Validation Specialist for Biotech and Aseptic Process
Solo para miembros registrados
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Validation Specialist. · ...
hace 1 mes
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. · ...
hace 3 semanas
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · The TOP Documentation Specialist is responsible for the collection, review, organization, and delivery of Turnover Packages (TOPs) for all packaging ...
hace 2 semanas
The Senior Engineering Specialist independently leads process optimization,troubleshooting,and engineering initiatives within manufacturing,pilot plant,operational or capital project environments. · ...
hace 2 semanas
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 ...
hace 2 semanas