Quality and Validation Engineer - Bayamón

We are seeking a Validation Engineer to support a short-term onsite project within a regulated medical device manufacturing environment. · Bachelor's degree in Engineering Mechanical Electrical or Chemical preferred · years of experience in validation life cycle process Equipment ...

This role involves planning, executing and documenting qualification and validation activities for equipment systems utilities and processes. · ...

Participate in validating various new products, qualifying new products and related design changes; ensure the overall quality of the products and minimize validation escapes to customers. · ...

We are seeking multiple Validation Engineers to support projects in Juncos, PR. · Develop and execute process validation documentation (IQ, OQ, PQ) · Develop and execute equipment qualification protocols (IQ, OQ, PQ) · ...

This is an exciting opportunity to participate in validating various new products ensuring overall quality and minimizing validation escapes to customers. · ...

Participate in validating various new products, qualifying new products and related design changes; ensure the overall quality of the products and minimize validation escapes to customersCreate validation testing schedule, perform tests and report test results to ensure that they ...

The Process Validation Engineer will support operations in a Medical Devices manufacturing environment. · Bachelor's degree in Engineering. · At least one (1) year of experience in Medical Device process and GMP-regulated environments. · ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for Commissioning and Qualification Owner for Capital Projects. · ...

We are seeking a detail-oriented Manufacturing Engineer / Validation Specialist to join our team. · The ideal candidate will be responsible for designing, implementing, and maintaining manufacturing processes in compliance with regulatory standards. · ...

We are seeking a self-sufficient Validation Engineer to support a downstream biologics validation project at a cGMP manufacturing site in Puerto Rico.The ideal candidate has hands-on experience validating downstream processes, equipment and instruments and can manage validation a ...

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. · ...

+Job summary · Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. · +Complete complex or novel assignments requir ...

Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments) skills to work. · ...

The Computer System Validation (CSV) Engineer will support the validation, testing, and documentation of computer systems to ensure compliance with regulatory and quality standards. · ...

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

A quality consulting group is looking for a talented validation engineer to join their team. They will work with a highly enthusiastic team contributing in the manufacturing industry in Puerto Rico and USA. · Perform and/or review process validation processes. · Experience in pro ...

+Job summary · Design manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing machining and material handling. · +Bachelor's Degree in Engineering. · ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the position of Validation Engineer / Specialist. · Bachelor's Degree in Science or Engineering. · Minimum of 2 years of experience in direct pharmaceutical medical device or b ...

<b>Job summary</b><br> · We are seeking an experienced CQV Project Manager to lead a full-scope Commissioning,, Qualification, ...

+We are seeking a Junior Validation Specialist with 2–3 years of experience to support commissioning, qualification, and validation activities at a biotech manufacturing site. · +Support preparation, execution, and review of validation documentation. · Assist with commissioning a ...