QA Engineer at Praxair

Tonawanda, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

22 May, 26

Salary

132000.0

Posted On

21 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

ISO9001 Auditing, FSSC22000 Knowledge, FDA Compliance, HPFBI Requirements, Facility Audits, Process Validation, Quality Assurance Program, COC/COA Oversight, Licensing Requirements, SOP Review, Incident Investigation, Problem Solving, Interpersonal Skills, Organizational Skills, Technical Knowledge, Regulatory Processes

Industry

Chemical Manufacturing

Description

Position Overview: Reporting to the Quality Assurance Manager, the Quality Assurance/Validation Engineer will assure compliance to ISO9001, FSSC22000, USA FDA, individual state, and applicable Canadian HPFBI requirements and conformance to customer quality standards. Responsibilities: Conduct LGUS facility audits to measure level of compliance to quality assurance standards. Complete medical process and information systems validation projects. Ensure that current regulatory requirements are reflected in the Quality Assurance Program. Provide QA support for plant personnel, Logistics, Sales, IT, Engineering, etc. Perform QA responsibilities, including COC/COA oversight, federal and state licensing requirements, customer correspondence and questionnaires, third party audit responses, and review of facility standard operating procedures. Ensure that quality incidents related to customer service, distribution, logistics, and production are investigated to drive process improvements. Participate in food and medical related CGA meetings. Qualifications: Bachelor’s or Master’s degree in Chemical, Mechanical, Electrical Engineering, or equivalent work experience. 5+ years Operations experience. 3+ years Quality Assurance experience. ISO9001 certified auditor and working knowledge of FSSC22000. State medical licensing and FDA registration renewal experience. Key elements of success include technical knowledge of the air separation and CO2 process, understanding of applicable regulatory processes, effective interpersonal, problem solving, and organizational skills. Ability to travel 20-25%25. About Linde: Linde is a leading global industrial gases and engineering company with 2024 sales of $33 billion. We live our mission of making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful and helping to sustain and protect our planet. Culture: At Linde, we strive to create a work environment that treats all employees with respect, supports new thoughts and ideas, encourages growth and development, celebrates our differences, and embraces inclusion. Linde is committed to remaining an employer of choice for the diverse, ever-increasing pool of global talent. For more information about the company and its products and services, please visit www.linde.com. Salary: Pay commensurate with experience. Open to salary range $90k - $132k. Benefits: Linde Gases US offers competitive compensation and an outstanding benefits package. Enjoy access to health, dental, disability, and life insurance, paid holidays and vacation, 401(k) matching, pension benefits, an employee discount program, and opportunities for educational and professional growth. Additional compensation may vary depending on the position and organizational level. Build your future with us while making an impact every day! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law. #LI-MM1

Responsibilities

The role involves conducting facility audits to ensure compliance with quality assurance standards like ISO9001 and FDA regulations, and completing validation projects for medical processes and information systems. Responsibilities also include providing QA support across various departments and overseeing documentation like Certificates of Conformance/Analysis.