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Katalyst Jobs in Chicago, IL (NOW HIRING)

Katalyst information

See Chicago, IL salary details

$52.5K

$95K

$150.9K

How much do katalyst jobs pay per year?

As of Aug 21, 2026, the average yearly pay for katalyst in Chicago, IL is $94,969.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $124,600.00 per year, depending on experience, location, and employer.

What is a Katalyst?

A Katalyst job typically refers to a role focused on driving change, innovation, or transformation within a company or industry. It may involve leadership, strategy development, and process optimization to improve efficiency and growth. Responsibilities can vary by organization but often include problem-solving, collaboration, and implementing new initiatives. The role is suited for individuals who excel at adapting to challenges and inspiring progress.

What are the typical responsibilities of a Katalyst on a daily basis?

As a Katalyst, your daily activities often include facilitating team meetings, monitoring project progress, identifying improvement opportunities, and communicating with stakeholders to align goals. You might also be responsible for implementing new processes, training team members, and resolving workflow bottlenecks to ensure smooth operations. Depending on the organization, you'll work closely with cross-functional teams to drive innovation and productivity. This dynamic role requires adaptability and proactive problem-solving to help teams reach their full potential.

What are the key skills and qualifications needed to thrive in the Katalyst position, and why are they important?

To thrive as a Katalyst, you need strong project management, strategic planning, and change management skills, usually backed by a bachelor’s degree in business or a related field. Familiarity with productivity tools like Microsoft Office Suite, collaboration platforms such as Slack or Asana, and process improvement certifications like Six Sigma can be highly beneficial. Exceptional communication, problem-solving, and leadership abilities help set top Katalysts apart. These skills are crucial because Katalysts are often responsible for driving organizational transformation and ensuring teams achieve shared objectives efficiently.

What are popular job titles related to Katalyst jobs in Chicago, IL?

For Katalyst jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Katalyst jobs in Chicago, IL look for?

The top searched job categories for Katalyst jobs in Chicago, IL are:

Infographic showing various Katalyst job openings in Chicago, IL as of August 2026, with employment types broken down into 95% Full Time, 3% Part Time, 1% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $94,969 per year, or $45.7 per hour.

Product Quality Engineer

Katalyst Healthcares and Lifesciences

North Chicago, IL • On-site

$69K - $89K/yr

Other

This job post has expired today. Applications are no longer accepted.


Job description

Summary :
  • The Quality Engineering Project Manager provides leadership, direction, and technical oversight for the Quality Engineering team within Operations.
  • This role leads quality engineers who support manufacturing processes and provide quality engineering expertise for product, process, equipment, utility, and facility-related activities.
  • The position ensures effective implementation of Client Quality Systems and supports validation, qualification, and risk-based compliance decisions across base business and development or market expansion initiatives.
  • The Quality Engineering Project Manager also manages functional resources and budget while maintaining strong quality, compliance, and operational performance.

Roles & Responsibilities :
  • Leads and develops a team of quality engineers supporting manufacturing process quality oversight, validation, qualification, and compliance activities.
  • Provides functional leadership for quality engineering activities across manufacturing processes, equipment, utilities, facilities, and associated systems.
  • Provides technical direction for quality engineering matters related to base business operations, development, tech transfer, and market expansion projects.
  • Ensures validation and qualification strategies, protocols, reports, and lifecycle activities are executed in accordance with Client Quality Systems, cGMP requirements, and applicable regulations.
  • Reviews quality and compliance gaps related to manufacturing processes, equipment, utilities, systems, and change controls, and drives appropriate risk-based actions.
  • Partners with Manufacturing, Validation, Engineering, Regulatory, Quality Systems, and Development to support compliant implementation of new and existing processes.
  • Guides risk management activities, including assessments, mitigation planning, and application of quality risk management principles.
  • Oversees or supports qualification and validation activities for equipment, processes, cleaning, utilities, computerized systems, and methods, as applicable.
  • Ensures quality engineering issues impacting product quality, process robustness, and regulatory compliance are identified, escalated, and resolved.
  • Communicates quality engineering status, key risks, trends, and recommendations to management and executive stakeholders, and manages functional resources and budget to support efficient execution.

Education & Experience :
  • Minimum Bachelor's degree required preferably in Physical or Life Sciences, Pharmacy, or Engineering
  • Certified Quality Engineer or formal training in quality engineering or statistics is preferred
  • 8+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics, device or chemical industry
  • 4+ years of supervisory/technical leadership experience
  • Must have a basic understanding and working knowledge of the physical and chemical characteristics of the products, including raw materials, manufactured at the plant.
  • Must be familiar with use of statistical quality systems, electronic document management and laboratory information management.
  • Must also be familiar with Quality policies as well as cGMP and other regulatory requirements.
  • Must have effective people management and communication skills necessary to supervise those reporting directly or through subordinates as well as establish and maintain effective working relationships among other key individuals in manufacturing, materials management, engineering, product development, Quality Systems, Product QA, Quality Control, Information Systems and Regulatory Affairs and must demonstrate sound judgment in evaluating and acting on day-to-day situations.
  • Strong communication Skills, both oral and written
  • Bachelor's, master's or PhD in a Life Science or Engineering is Highly Desired.
  • Demonstrated strategic vision and leadership in building and sustaining a high-performing team responsible for managing base business priorities, site-related projects, compliance remediation activities, and global project deliverables is Highly Desired.
  • Strong cross-functional collaboration and negotiation skills, with the ability to influence stakeholders, align priorities, and drive effective outcomes across complex and diverse functional teams is Highly Desired.