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Process Control Manager Jobs in New York (NOW HIRING)

Quality Control Manager

Manhattan, NY · On-site

$128K - $155K/yr

Manages the activities of the quality control team to ensure that the work product meets the ... processes to meet or exceed quality goals, expectations, and plans * Oversees quality testing and ...

WHAT WE ARE HUNGRY FOR The position of Quality Control Manager is responsible for auditing Paris ... processes, sanitation, quality programs • Knowledge of food production techniques, food ...

We are actively seeking a dedicated and results-driven Quality Control Manager. In this role, you ... Oversee incoming, in-process, and final inspection strategies, ensuring appropriate controls ...

Showing results 21-40

Process Control Manager information

See New York salary details

$41K

$110.4K

$152.1K

How much do process control manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for process control manager in New York is $110,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,500.00 and $123,600.00 per year, depending on experience, location, and employer.

What is a process control manager?

A Process Control Manager is responsible for overseeing and optimizing the various control systems and processes used in manufacturing or industrial operations. Their role involves ensuring that production processes run smoothly, efficiently, and safely by managing automated systems, monitoring performance, and implementing improvements. They often work closely with engineering, production, and quality assurance teams to identify issues and enhance process reliability. Additionally, they may be involved in training staff, maintaining compliance with regulations, and deploying new technologies to improve process control.

What are the key skills and qualifications needed to thrive as a process control manager?

To thrive as a Process Control Manager, you need a strong background in engineering or process technology, analytical problem-solving abilities, and experience in manufacturing or industrial environments. Familiarity with distributed control systems (DCS), programmable logic controllers (PLCs), process automation software, and often certifications like Six Sigma or PMP are highly valued. Excellent leadership, communication, and decision-making skills help manage teams and coordinate with cross-functional departments effectively. These competencies are vital for ensuring process efficiency, safety, quality, and continuous improvement within complex production operations.

What are some typical challenges a process control manager might face in a manufacturing environment?

Process Control Managers often encounter challenges such as integrating new technologies with legacy systems, maintaining process consistency across shifts, and troubleshooting unexpected process deviations. They must also ensure compliance with safety and quality standards while coordinating closely with engineering, production, and maintenance teams. Strong problem-solving skills and effective communication are essential for navigating these complexities and driving continuous improvement initiatives.

What is the difference between Process Control Manager vs Process Engineer?

AspectProcess Control ManagerProcess Engineer
CredentialsBachelor's degree in engineering, certifications in process control (e.g., Certified Control Systems Technician)Bachelor's or master's in chemical, mechanical, or industrial engineering; certifications vary
Work EnvironmentSupervises control systems teams, manages process control strategies in manufacturing plantsDesigns, develops, and optimizes manufacturing processes, often in labs or plant settings
Employer & IndustryManufacturing, oil & gas, chemical industriesChemical, pharmaceutical, manufacturing industries

The Process Control Manager oversees the implementation and maintenance of control systems, focusing on team management and strategy. In contrast, the Process Engineer concentrates on designing and improving processes. Both roles require technical expertise but differ in scope and responsibilities.

What are the most commonly searched types of Process Control jobs in New York?

The most popular types of Process Control jobs in New York are:

What are popular job titles related to Process Control Manager jobs in New York?

For Process Control Manager jobs in New York, the most frequently searched job titles are:

What cities in New York are hiring for Process Control Manager jobs?

Cities in New York with the most Process Control Manager job openings:

Infographic showing various Process Control Manager job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $110,418 per year, or $53.1 per hour.

Quality Assurance Process Control Engineer

Parsippany Troy Hills, NJ • On-site

Other

Posted 22 days ago


Job description

Job Summary

The QA Process Control Engineer is responsible for ensuring that all sterilization processes and microbiological testing meet the highest regulatory and quality standards. This role involves managing sterilization cycle validations, maintenance, and evaluations, overseeing product release procedures related to cleaning and sterilization.

Responsibilities Regulatory & Quality Compliance:
  • Ensure full adherence to all applicable regulatory and quality system requirements related to the cleaning and sterilization of Onkos product.
  • Regularly review and update documentation and procedures to align with FDA-QSR, ISO, AAMI, and other relevant guidelines.
Sterilization Controls:
  • Oversee routine sterilization validations, cycle maintenance, and cycle evaluations to guarantee product sterility and regulatory compliance.
  • Critically analyze processes regarding sterilization controls, environmental monitoring programs, and product disposition.
  • Evaluate proposed process changes and assess their impact on current sterilization controls.
  • Oversee the timely execution and documentation of quarterly dose audits.
New Product Initiation & Validation:
  • Work with Product Development in validating and adopting cleaning protocols and sterilization processes for product launches.
  • Collaborate with cross-functional teams to ensure that new products meet rigorous cleaning and sterilization standards while integrating with existing quality systems.
Documentation & Auditing:
  • Maintain comprehensive documentation related to sterilization processes, controlled environment areas, and final product release procedures.
  • Monitor system performance via monthly reports, audits, and batch record reviews to identify opportunities for process improvement.
Risk Management & Investigations:
  • Perform risk assessments, conduct non-conformance investigations, and lead CAPA projects as required.
  • Participate in product quality trend analysis and guidance of corrective actions.
Process Development:
  • Define, document, and implement procedures for sterility assurance, environmental controlled areas, and product disposition.
  • Assist Quality team leadership in the development and maintenance of policies and practices governing behavior, control, and access within Controlled Environment Areas.
Authority & Decision-Making:
  • Exercise the authority to recommend and initiate preventive and corrective actions related to product non-conformance and other quality system activities.
Requirements
  • Minimum of 5 years of experience in cleaning and sterilization within the medical manufacturing or pharmaceutical industry.
  • Extensive understanding of microbiological and sterilization testing, including hands-on experience with sterilization cycle validations and environmental monitoring.
  • Proven ability to execute sterility tests and manage sterilization controls effectively.
  • Must be well-versed in the following sterilization modalities: ethylene oxide, gamma, and steam.
  • Familiarity with FDA regulations, USP, ISO standards, and quality management systems (e.g., ISO 13485).
About Onkos

At Onkos Surgical, we believe individuals with cancer requiring surgery deserve solutions designed specifically for them. These individuals, their caregivers and their support network deserve an organization passionately championing their cause.

At Onkos Surgical, we exist to maintain a singular focus on surgical oncology by looking at everything we do through the lens of the cancer surgeon and their patients.

At Onkos Surgical, we will:

  • Find solutions to our patients’ unmet clinical needs and advocate for their cause.
  • Partner with surgical oncologists through research, education and innovation, to treat their patients more effectively and more efficiently.
  • Collaborate with regulatory agencies to find pathways to provide timely solutions while upholding the highest standards of quality or compliance.
  • Fulfill our employees’ desire to make a difference in the lives of the patients they serve while achieving their own professional growth.
  • Deliver value to our customers and shareholders.
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