Technical Quality Assurance Specialist

Job OverviewWe are seeking a highly skilled Quality Assurance Engineer to join our team at Flexible & Integrated Technical Services, LLC. As a Quality Assurance Engineer, you will play a crucial role in ensuring the quality and compliance of our manufacturing processes.

Job SummaryWe are seeking a highly skilled and detail-oriented Senior Quality Assurance Specialist to join our team. In this role, you will be responsible for ensuring the quality of our products throughout the production process.About UsAt Integra LifeSciences, we are committed to providing high-quality medical devices that improve patient outcomes. Our...

Job Title: Quality Assurance EngineerWe are seeking a highly skilled Quality Assurance Engineer to join our team. In this role, you will be responsible for ensuring the quality of our products throughout the production process.About UsAt Integra LifeSciences, we are committed to providing high-quality medical devices that improve patient outcomes. Our team...

Job SummaryWe are seeking a highly skilled Project Manager to lead a large-scale, multi-million-dollar project within the medical device sector. The right candidate will have extensive experience managing complex projects, budgets, cross-functional teams, and ensuring compliance with industry regulations.ResponsibilitiesDevelop comprehensive project plans,...

About UsComputer Integration Of Quality Assurance Inc. is a leading company in the medical device sector, dedicated to developing innovative solutions that improve patient outcomes. Our team is comprised of experienced professionals who share a passion for quality assurance and customer satisfaction.This role offers an exceptional opportunity to join our...

For Quality Engineering services in the Manufacturing area.  WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's degree in Sciences or Engineering and previous exposure in Quality Engineering activities within the Medical Devices or Pharmaceutical industry.Excellent computer skills Bilingual: Spanish and English (verbal/ written) Shift: Administrative...

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...

Job SummaryWe are seeking a highly skilled Project Manager to lead a large-scale, multi-million-dollar project within the medical device sector. The right candidate will have extensive experience managing complex projects, budgets, cross-functional teams, and ensuring compliance with industry regulations. This role requires a proactive leader with strong...

**Job Overview:**We are seeking a highly motivated and skilled Project Implementation Specialist to support the successful deployment of an Oracle-based on-demand label printing application at our site.**Responsibilities:* Coordinate communication between Corporate IT, Oracle implementation teams, and site stakeholders (IT, QA, and Manufacturing).* Serve as...

**Job Title:** Oracle Labeling System ManagerWe are seeking a highly experienced Oracle Labeling System Manager to join our team at Computer Integration Of Quality Assurance Inc. The ideal candidate will have a strong background in Oracle system implementation and management, as well as excellent communication and interpersonal skills.**Responsibilities:*...

Support the execution of equipment, facility, and utilities validation studies;Create and revise protocols and reports using technical writing skills;Oversee and assist engineers with their assigned projects;Participate in developments/improvements to validation programs as needed;Requirements:Bachelor's degree in Engineering;Previous exposure to validation...

Job Overview: We are seeking a highly skilled Project Manager to lead our team in delivering high-quality projects within the regulated industry. As a Project Manager, you will be responsible for developing and implementing project plans, managing budgets, and ensuring regulatory compliance.Key Responsibilities:Develop comprehensive project plans that...

OverviewLabchems Corp. is a dynamic and innovative company dedicated to delivering high-quality medical devices and pharmaceuticals to the market. We are committed to excellence in quality, safety, and customer satisfaction.Job SummaryWe are seeking a highly skilled Medical Device Validation Specialist to join our quality assurance department. The successful...

For Project Management services in the Facilities area.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree in Life Sciences, Engineering, or related field and at least five (5) years of previous exposure to Project Management activities within the regulated industry.Bilingual: (Spanish and English) Shift: Administrative & according to business...

About Labchems Corp.We are a leading manufacturer of medical devices and pharmaceuticals seeking a highly skilled Medical Device Validation Specialist to join our team. As a key member of our quality assurance department, you will play a crucial role in ensuring compliance with EU MDR regulations.Responsibilities:Support the EU MDR program by participating...

Key ResponsibilitiesInvestigate manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations)Analyze results and make recommendationsDevelop reports and optimize Manufacturing processes using engineering methods (e.g., SIX Sigma and LEAN methods)IDentify opportunities for basic equipment, tools, fixtures, etc. to...

About the RoleThe ideal candidate will have a Bachelor's degree in Sciences or Engineering and previous exposure in Quality Engineering activities within the Medical Devices or Pharmaceutical industry. They will be responsible for investigating manufacturing product quality and compliance issues, analyzing results, making recommendations, and developing...

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...

At Labchems Corp., we are seeking a highly skilled Project Validation Specialist to support the efficient and timely completion of projects related to sterilization areas. This includes new Ethylene oxide sterilization cycle validation, existing Ethylene oxide sterilization cycle re-validation, and sterilization cycle improvements.This role requires a...

Project Management Role: We are seeking an experienced Project Manager to join our team. In this role, you will be responsible for planning, executing, and monitoring projects from start to finish. You will work closely with cross-functional teams to ensure successful project delivery.Responsibilities:Plan and coordinate project activities, including...