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IDEX

Manufacturing Engineer - High Purity

Farmington, CT · On-site

$88.20K - $132.20K/yr

As a Manufacturing Engineer supporting High Purity cleanroom operations , you will shape processes, strengthen reliability, and enable production teams to operate safely, consistently, and ...

High Purity Solutions

Pipe Fitters

Elkridge, MD

$36 - $45/hr

High Purity Solutions. * Salary/Pay Rate: $36.00 to $45.00 per hour plus Performance Based Bonus. * Location: Elkridge, MD. (travel required) * Job/Employment Type: Full Time. * Schedule: Monday ...

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How much do high purity jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for high purity in the United States is $20.47, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $24.28 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a High Purity Technician, and why are they important?

To thrive as a High Purity Technician, you need a solid understanding of cleanroom protocols, fluid systems, and industry safety standards, typically with a background in mechanical, chemical, or process technology. Familiarity with tools such as orbital welders, leak detection instruments, and common high-purity piping systems (e.g., stainless steel, PVDF) is essential, and certifications like ASME or semiconductor fabrication training can be advantageous. Attention to detail, problem-solving abilities, and strong teamwork are crucial soft skills in this precision-driven environment. These competencies ensure the safe, efficient, and contamination-free installation and maintenance of high-purity systems vital to industries like semiconductor manufacturing, pharmaceuticals, and biotech.

What are some common challenges faced by professionals in High Purity piping or process installation roles, and how can they be addressed?

Professionals working in High Purity piping or process installation often encounter challenges such as maintaining contamination-free environments, adhering to strict industry standards (like ASME BPE), and ensuring precise documentation for traceability. Managing these challenges requires meticulous attention to detail, thorough knowledge of cleanroom protocols, and effective communication within multidisciplinary teams including engineers, quality assurance, and safety personnel. Building expertise through specialized training and staying updated on evolving regulations helps professionals excel and advance in this highly technical field.

What is a High Purity technician?

A High Purity technician is a skilled professional who specializes in the installation, maintenance, and repair of high purity piping systems. These systems are commonly used in industries such as pharmaceuticals, biotechnology, and semiconductor manufacturing, where contaminants must be kept to an absolute minimum. High Purity technicians work with specialized materials like stainless steel and plastic piping to ensure that gases and liquids remain uncontaminated throughout production processes. Their role is critical to maintaining the integrity and quality of sensitive manufacturing environments.

What is the difference between High Purity vs Cleanroom Technician?

AspectHigh PurityCleanroom Technician
Required CredentialsCertifications in cleanroom protocols, quality control, and sometimes technical degreesCertifications in cleanroom procedures, safety, and sometimes technical or technical-related degrees
Work EnvironmentHighly controlled, contamination-sensitive environments, often in semiconductor, pharmaceutical, or biotech industriesCleanroom settings with strict contamination controls, working in manufacturing or assembly lines
Industry UsageCommonly used in semiconductor manufacturing, pharmaceuticals, and biotech sectorsUsed across electronics, pharmaceuticals, and biotech industries

High Purity specialists focus on maintaining ultra-clean environments and handling materials with minimal contamination, often requiring advanced certifications. Cleanroom Technicians perform routine tasks within controlled environments, ensuring cleanliness and compliance. While both roles operate in cleanroom settings, High Purity roles typically demand higher technical expertise and certifications, emphasizing contamination prevention at a more advanced level.

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What job categories do people searching High Purity jobs look for? The top searched job categories for High Purity jobs are:
High Purity jobs near you
Infographic showing various High Purity job openings in the United States as of May 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $42,583 per year, or $20.5 per hour.

Process Controls Engineer - High Purity Water Subsystems

DEKA

Manchester, NH • On-site

Full-time

Posted 5 days ago

Job description

We are looking for a Process Controls Engineer to own the design, integration, and qualification of high purity water subsystems embedded within a complex, multi-disciplinary regulated device platform. You will play a critical role in ensuring onboard water purity performance, subsystem reliability, and regulatory compliance across the full device development lifecycle.
How you will make an impact as a Process Controls Engineer:
  • Define process control architecture for onboard high purity water generation, purification, storage, distribution, and quality monitoring systems, and develop control specifications that drive consistency and compliance across the subsystem and its interfaces with the broader device.
  • Architect control interfaces between the water subsystem and the host device's embedded controls, sensor networks, onboard diagnostics, and cloud monitoring platforms.
  • Own subsystem requirements and control narratives end-to-end, from concept through IQ/OQ/PQ qualification and routine water quality monitoring.
  • Lead hazard analysis and risk management per ISO 14971, identifying and mitigating risks to water purity integrity, sterility, device performance, and patient safety.
  • Drive subsystem validation strategies covering statistical process control, data integrity (21 CFR Part 11), conductivity and TOC monitoring, microbial and endotoxin control, WFI qualification, and fluid pathway integrity testing.
  • Guide cross-functional teams across fluidics, electrical, embedded software, and manufacturing, balancing purity performance against device-level SWaP, cost, and manufacturability constraints.
  • Contribute to DHF documentation, PFMEA reviews, design reviews, and traceability matrices throughout the device development program.
  • Support program management by estimating effort, surfacing technical risks, and aligning project plans with qualification and regulatory milestones.

Required Qualifications:
  • BS or MS in Controls Engineering, Chemical Engineering, Mechanical Engineering, Biomedical Engineering, or related discipline.
  • 2+ years in a regulated device development environment with hands-on experience designing, integrating, and qualifying high purity water or fluid handling subsystems.
  • Working knowledge of WFI and purified water generation technologies (RO, EDI, ultrafiltration, distillation), onboard distribution system design, and inline water quality monitoring.
  • Regulatory fluency across USP <1231>, USP <645>, USP <643>, USP <85>, 21 CFR Parts 210/211/820, 21 CFR Part 11, GAMP 5, ISO 13485, and ISO 14971.
  • Hands-on experience with FMEA, DFMEA, PFMEA, hazard analysis, and IQ/OQ/PQ protocol development and execution.
  • Proven ability to guide cross-functional teams and drive alignment across quality, regulatory, fluidics, software, and manufacturing stakeholders.
  • Strong written and verbal communication skills with the ability to support presenting complex subsystem data to regulatory bodies and executive leadership.

Preferred Qualifications:
  • Experience with onboard WFI generation and sterile water subsystems within aseptic processing or drug delivery devices.
  • Familiarity with cloud-connected water quality monitoring, remote diagnostics, and cybersecurity considerations for networked subsystems.
  • Experience supporting FDA or EMA regulatory inspections related to high purity water system qualification and monitoring.
  • Knowledge of SWaP-optimized purification technologies and miniaturized onboard water system design.
  • Familiarity with MBSE methodologies (SysML, Cameo) for subsystem interface definition and requirements traceability.

About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.

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