Process Validation Engineer

Process Improvement Engineer Job Description">Labchems Corp. is seeking a Process Improvement Engineer to drive quality excellence in our facilities and construction projects. As a key member of the Core Team, you will develop and implement quality programs, analyze data, and identify areas for improvement. Your primary responsibilities include developing...

Job OverviewLabchems Corp. is seeking a highly skilled Medical Device Validation Engineer to support the European Union Medical Device Regulation (EU MDR) program.About the RoleThe successful candidate will participate in data gathering, gap assessments, remediation planning, and documentation generation and execution for EU MDR compliance.Key...

**About Us:**Labchems Corp. is a leading organization in the industry, committed to delivering high-quality products and services.We are seeking a skilled Senior Validation Engineer to join our team and contribute to our mission.This role involves supporting facilities and construction projects, mainly in Collagen areas, by participating in meetings and...

For Validation Engineering services in the Facilities area.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree in Engineering or related field and at least three (3) years of previous exposure to Validation  activities within the regulated industry.Bilingual: (Spanish and English) Shift: Administrative & according to business needs  Experience...

Quality Engineer (QE) resource will be allocated to work with the facilities/construction projects, mainly in Collagen Manufacturing areas. The QE resource is required to be part of the Core Team of the facilities projects, participate on meetings and to review and approve all documentation required such as PCDT, Change Control, EMPQ, equipment...

For Validation services in the Facilities area.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's degree in Engineering and a minimum of five (5) years of exposure in Validation activities within the Pharmaceutical or Medical Device Industry.Excellent verbal/written communication skills (English and Spanish)  Shift: Administrative & according to...

Support the European Union Medical Device Regulation (EU MDR) program with 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 (drawings, specifications, bill of materials, production...

EQVAL Consulting Group, Inc.  is a company that provides services to the manufacturing industry ( Medical Devices, Pharmaceuticals, Biotechnologies, others ).We work with an extraordinary group of professionals ( employees and contractors ) to accomplish the requirements established by our customers, in order to perform and provide a highly effective...

For Validation & Quality services in the Engineering & Manufacturing areas.  WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree in Engineering and previous exposure to validation and/or quality activities within the Pharmaceutical or Medical Devices industry.  Bilingual, Spanish and English (good communication) Shift: Administrative & according...

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...

Job RequirementsWe are seeking an experienced Quality Assurance and Validation Lead to join our team. The successful candidate will be responsible for ensuring the quality and integrity of our products and processes.About the RoleThe Quality Assurance and Validation Lead will be responsible for:Supporting the development and implementation of quality and...

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...

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...

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...

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...

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:...

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...

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...

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...