Project Validation Specialist Iii

At Labchems Corp., we are seeking a Senior Validation Specialist to support the efficient completion of project-related tasks for the sterilization area. This includes new Ethylene oxide sterilization cycle validation, existing Ethylene oxide sterilization cycle re-validation, and sterilization cycle improvements.The ideal candidate will have advanced...

The position is to support the European Union Medical Device Regulation (EU MDR) program. The incumbent will be supporting the following activities: -- Data Gathering-Participate in the discovery and compilation of required documentation to be evaluated. -- Gap Assessments-Assess of all manufacturing documentation such as product device master record...

Support CORPORATE STERILIZATION WORKSTREAM for efficient and timely completion of project related to sterilization area including, new Ethylene oxide sterilization cycle validation, existing Ethylene oxide sterilization cycle re-validation, and sterilization cycle improvements, among others. Interprets microbiological testing data, monitors, and maintains...

Company OverviewLabchems Corp. is a leading manufacturer of high-quality laboratory chemicals and equipment. Our commitment to innovation and customer satisfaction has earned us a reputation as a trusted partner in the scientific community.Job DescriptionWe are seeking a highly skilled EU MDR Compliance Specialist III to join our team. The successful...

Labchems Corp. seeks a highly skilled Validation Specialist to join our team in supporting the EU MDR program. As a key member of our team, you will be responsible for ensuring compliance with EU MDR regulations by conducting thorough gap assessments and developing comprehensive remediation plans. Your expertise in validation activities, project management,...

The position is to support the implementation of labeling / artwork changes on Duragen product family for CE and non-CE marked SKUs. The incumbent will be supporting the following activities to ensure conformance with global labeling SOP for Duragen products manufactured at Integra Añasco.• Data Gathering – Participate in the discovery and compilation...

We are a Service Provider company different from the rest. Flexible & Integrated Technical Services, Llc prides ourselves in how we treat the most important piece of our company's puzzle: you**Job Summary:**This role will be responsible for ensuring timely and thorough execution of Computer System Validation protocols, meeting FDA requirements. You will...

We are seeking a Validation and Sterilization Professional to support our corporate sterilization workstream. As a senior-level professional, you will be responsible for supporting the efficient completion of project-related tasks for the sterilization area.This includes new Ethylene oxide sterilization cycle validation, existing Ethylene oxide sterilization...

Support facilities/construction projects, mainly in Collagen areas. Required to be part of the Core Team of the facilities projects, participate on meetings and review/approve all documentation required such as PCDT, Change Control, EMPQ, equipment qualifications, documents changes, RM changes, calibration/PM documents. Will develop technical documentation:...

Job DescriptionWrite, execute and maintain validation protocols on a timely basis.Ensure thorough and complete execution of all protocols, meeting FDA requirements.Develop documentation of investigations and communicate findings to minimize chance of recurrence.This role requires strong technical skills in SOP development, validation documentation, GMP and...

We are seeking a highly experienced EU MDR Compliance Specialist to join our team at Labchems Corp. As a critical member of our compliance team, you will be responsible for ensuring that our company remains compliant with EU MDR regulations. Your expertise in validation activities, project management, and technical documentation will be essential in...

The role of this position is to provide support to the European Union Medical Device Regulation (EU MDR) program at Labchems Corp. The successful candidate will be responsible for participating in data gathering and compilation of required documentation, conducting gap assessments on manufacturing documentation, and performing remediation tasks.Key...

As a Validation & Quality Engineer at Flexible & Integrated Technical Services, LLC, you will be an integral part of our team, contributing to the success of our clients in the Pharmaceutical, Medical Device, and Manufacturing industries. Key responsibilities include:Developing SOPs and ensuring compliance with regulatory guidelinesSupporting the execution...

**Job Summary:**Labchems Corp. seeks a highly skilled Quality Assurance Specialist to support our facilities and construction projects in Collagen areas.The ideal candidate will be part of the Core Team, participating in meetings and reviewing/approving all documentation required for project success.This role involves developing technical documentation,...

Job Overview">At Labchems Corp., we are seeking a highly skilled Quality Assurance Specialist to support our facilities and construction projects. As a key member of the Core Team, you will participate in meetings and review/approve all documentation required for facility projects. Your primary responsibilities include developing technical documentation,...

Job Overview: Kelly Science, Engineering, Technology & Telecom is seeking a highly skilled Senior Quality Assurance Specialist to join our team. This role will be allocated to work with facilities and construction projects in Collagen Manufacturing areas.Main Responsibilities: The successful candidate will participate in meetings, review and approve...

Job Description:Labchems Corp. is seeking a highly skilled Production Process Specialist - Life Cycle Management to join our Engineering team.About the Role:This position will work closely with cross-functional teams to support design changes impacting operations, manufacturing, launch readiness, and production stability requirements of existing products.The...

Labchems Corp. is looking for a Sterilization Process Expert to join our team. As a key member of our sterilization workstream, you will be responsible for ensuring the efficient and timely completion of project-related tasks.Key responsibilities include interpreting microbiological testing data, monitoring and maintaining sterility assurance, and conducting...

For Computer System Validation and Software services in the Manufacturing area.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree in Life Sciences or Engineering and previous exposure in Computer System Validation activities within the regulated industry.Bilingual, Spanish, and English.Shift: Administrative & according to business needs ...

We are Flexible & Integrated Technical Services, LLC, a service provider company offering Engineering, Construction, Maintenance, Utilities, and Specialized Technical services across the island and in the US. As a Validation & Quality Engineer, you will play a crucial role in our team by supporting engineering department operations, managing quality systems,...