MF01-041122 Validation Project Manager - Gurabo, PR

We are seeking a highly skilled and experienced Project Manager to oversee and manage construction projects from inception to completion. · ...

We are seeking a talented individual committed to work under the highest ethics standards for the following position: · CQV Project Manager responsible for leading CQV activities for a biotechnology manufacturing project. · ...

C&Q Engineers will be responsible for generating design documents, authoring protocols, and executing commissioning and qualification activities. · ...

We are seeking a C&Q specialist to join our team at PharmEng Technology. The ideal candidate will have experience in commissioning and qualification, validation, quality systems, regulatory affairs, engineering, and training. They will be responsible for generating design documen ...

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

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position: CQV Lead – Upstream & Downstream Biotech Process Equipment. · ...

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., ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · CIP/SIP CQV Lead for Biotech · ...

We are seeking a talented individual for the C&Q Lead – Inspection Lines position to oversee commissioning and qualification activities for visual inspection systems in sterile drug product operations. · Key Responsibilities · Lead end-to-end C&Q scope for automated and semi-auto ...

We have an opening position to join our team as Quality and Scheduling Manager. · Oversee and coordinate with Plant Manager scheduling for the manufacturing plantOversee a team of employeesAssist on a daily production scheduleResponsible for shipping coordinationPrepare shipping ...

We're looking for experienced carpenters with experience in general construction projects. · ...

+Job summary · We are seeking for talented individuals who is committed to work under the highest standards of ethics. · +ResponsibilitiesPackaging Validation · ...

Cleaner Validation Scientist is being sought by Validation & Engineering Group Inc to provide solutions in Pharmaceutical industries. · ...

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. · Author, review, and execute commissioning and qualification protocols ( ...

Job summaryWe are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position: · CQV Specialist for Biotech Downstream Process Equipment · ...

We are seeking for talented, dedicated individuals who are committed to work under the highest standards of ethics and with expertise in commissioning and qualification of facilities. · Responsibilities include developing and reviewing mechanical completion plans, · ensuring qual ...

The Automation Engineer will be responsible for automating software programs and writing automation scripts. · ...

We are seeking an experienced Automation Engineer to join our team at PharmEng Technology. Responsibilities include drawing up ideas for automated software testing procedures, automating software programs and writing automation scripts. · Bachelor's Degree in Engineering  · ...