Quality Assurance Associate

• You will support and lead quality investigations involving defects, non-conformances, deviations, complaints, and adverse events, ensuring timely corrective actions, reporting, data trending, and resolution.
• Assists in internal and supplier audits and establishing/updating supplier and component specifications and testing as needed.
• Ensures labels are appropriately reviewed and approved for use and meet all internal and external requirements
• You will review all steps performed and ensures that the step in the manufacturing process has taken place as defined in the Batch Production Record.
• Reports findings of in-process errors and provides follow-up to ensure adequate completion of corrective actions.
• Ensures for product disposition, e.g., approvals for release, distribution or rejection.
• Perform statistical analyses of processes as required to meet quality control standards.
• Ensure timely throughput of product through lab work queue.
• Comprehensive familiarity with the lab scope and all associated lab documentation and procedures.
• Operate required analytical instrumentation (GCs, FTIRs, process analyzers, etc.).
• You will report problems with analytical instrumentation and assist in subsequent repair(s).
• Accurately input and document analytical data into all necessary analytical and plant process logs.
• You must strictly adhere to all necessary calibration requirements within all lab operations.
• Must be willing and able to work in a highly structured work environment with regard to safe and consistent conformance to operating procedures and work practices.
• Conforms to ISO 9001:2008 directives included but not limited to policy and procedures.
• You will support initiatives in Continuous Quality Improvement.
• Through observation of work area(s), is alert to and avoid unsafe behaviors and conditions or other hazards.
• Follows all safety rules/regulations and immediately reports infractions and/or workplace injuries/accidents to proper personnel.

• You need experience in laboratory testing, quality assurance, or a related technical field.
• Strong understanding of analytical methods, instrumentation, and data interpretation.
• You will have the ability to work independently and make quality‑driven decisions.
• Excellent documentation, communication, and organizational skills.
• Familiarity with GMP, ISO, FDA, or similar regulatory frameworks.

• You have prior experience in industrial gases, pharmaceuticals, food manufacturing, or regulated environments.
• Experience supporting investigations, CAPA, or quality audits.
• Technical training or certification in laboratory sciences or quality systems.

Linde is a leading global industrial gases and engineering company with 2025 sales of $34 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, decarbonize and protect our planet.

Linde serves a variety of end markets such as chemicals & energy, food & beverage, electronics, healthcare, manufacturing, metals and mining. Linde’s industrial gases and technologies are used in countless applications, enabling space exploration and launch technologies, delivering ultra-high-purity and specialty gases for semiconductor manufacturing, providing life-saving medical oxygen and enabling clean hydrogen production and carbon capture to reduce greenhouse gas emissions.

Linde also delivers state-of-the-art gas processing solutions to support customer growth, efficiency improvements and emissions reductions.

At Linde, the sky is not the limit. If you’re looking to build a career where your work…