MV01-101325 Manufacturing Engineer / Validation Specialist - Guaynabo

+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 ...

We are seeking a talented Validation Specialist (Packaging) dedicated to working under high ethics standards. · ...

This is a validation specialist role with experience in regulated industry validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities. The candidate should have a bachelor's degree in engineering or sciences and at least five years of ...

Validation Specialist with experience in regulated industry validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities. · Change ControlEquipment qualification (manufacturing and laboratory) ...

Validation Specialist with experience in regulated industry validating/qualifying laboratory equipment manufacturing equipment processes utilities and facilities. · Execute complete validation cycle · Change Control · Equipment qualification manufacturing and laboratory) · ...

The Validation Specialist is responsible for planning, executing and documenting qualification and validation activities to ensure that equipment systems utilities and processes meet regulatory requirements and industry standards. · Develop and execute validation protocols (IQ/OQ ...

For Process Validation services in the manufacturing area. · ...

This resource will attend all related meetings and provide support to qualification/validation activities. Will also work directly with the review of raw data and development of completion reports. · Bachelor in Engineering · 5 years of experience as validation consultant in regu ...

This resource will provide support to qualification/validation activities related to manufacturing equipment. · ...

We Are Seeking For Talented Dedicated Individuals Who Is Committed To Work Under The Highest Standards Of Ethics To And With Expertise In The Following Areas: · Packaging Validation · ...

Mentor Technical Group provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. · ...

A highly motivated and enthusiastic individual to join our team in a world-class manufacturing industry. · Perform and/or review process validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [ · [URS, FAT, IQ] · ...

For Validation services in the Sterile and Filling area. · Develop,, · ...

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 ...

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 individual committed to work under the highest ethics standards for the position of Senior Cleaning Validation Specialist. · ...

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 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 ...

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 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. · ...