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Process Engineer Manager Jobs in Saint Louis, MO

Kindeva Drug Delivery

Process Engineer

Brentwood, MO · On-site

The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP , FDA , EMA , ISO , and other ...

kindeva

Process Engineer

Brentwood, MO · On-site

The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP , FDA , EMA , ISO , and other ...

Cement Recruiter

Process Engineer

Festus, MO

Louis) is searching for an experienced Process Engineer to join our team. Responsibilities include ... for Production Manager as necessary Conduct or attend weekly safety meetings; inspect the ...

kindeva

Process Engineer

Brentwood, MO

The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP , FDA , EMA , ISO , and other ...

kindeva

Process Engineer

Brentwood, MO · On-site

The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP , FDA , EMA , ISO , and other ...

kindeva

Process Engineer

Brentwood, MO · On-site

The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP , FDA , EMA , ISO , and other ...

Buzzi Unicem USA, Inc.

Process Engineer

Festus, MO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Louis) is searching for an experienced Process Engineer to join our team. Responsibilities include ... for Production Manager as necessary * Conduct or attend weekly safety meetings; inspect the ...

Buzzi Unicem USA, Inc.

Process Engineer

Festus, MO

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Louis) is searching for an experienced Process Engineer to join our team. Responsibilities include ... for Production Manager as necessary * Conduct or attend weekly safety meetings; inspect the ...

Buzzi Unicem USA, Inc.

Process Engineer

Festus, MO

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Louis) is searching for an experienced Process Engineer to join our team. Responsibilities include ... for Production Manager as necessary * Conduct or attend weekly safety meetings; inspect the ...

Black & Veatch

Wastewater Process Engineer

Creve Coeur, MO · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Engages on collection, assimilation, analysis, and management of data for process modeling and design work * Prepares process models and carries out complex engineering calculations following ...

CRB

Process Engineer II

Saint Louis, MO · On-site

This position is responsible for managing scope, budget, and schedule for assigned work, which typically involves small to medium-sized projects of moderate complexity. The Process Engineer III works ...

CRB

Process Engineer II

Saint Louis, MO · On-site

This position is responsible for managing scope, budget, and schedule for assigned work, which typically involves small to medium-sized projects of moderate complexity. The Process Engineer III works ...

CRB

Process Engineer II

Saint Louis, MO · On-site

This position is responsible for managing scope, budget, and schedule for assigned work, which typically involves small to medium-sized projects of moderate complexity. The Process Engineer III works ...

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Showing results 1-20

All JobsProcess Engineer JobsProcess Engineer Manager JobsProcess Engineer Manager Jobs in Saint Louis, MO

Process Engineer Manager information

See Saint Louis, MO salary details

$48.1K

$89.5K

$138.5K

How much do process engineer manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for process engineer manager in Saint Louis, MO is $89,462.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $100,100.00 per year, depending on experience, location, and employer.

What is a process engineer manager?

Process Engineer Managers are professionals responsible for overseeing and improving manufacturing or production processes within an organization. They lead teams of process engineers, coordinate projects aimed at optimizing efficiency, quality, and safety, and ensure compliance with industry standards. Their role often involves analyzing workflows, implementing new technologies, and collaborating with other departments to achieve organizational goals. Additionally, they may manage budgets, provide technical support, and mentor junior engineers.

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

AspectProcess EngineerProcess Engineer Manager
ResponsibilitiesDesign, optimize, and implement manufacturing processesOversee process engineering teams, develop strategies, and ensure project delivery
Required SkillsProcess design, problem-solving, technical knowledgeLeadership, project management, technical expertise
CertificationsPE license often preferred, Six Sigma, Lean certificationsSame as Process Engineer, plus management training
Work EnvironmentManufacturing plants, engineering officesManufacturing plants, engineering departments, management offices

The main difference is that Process Engineer Managers lead teams and develop strategies, while Process Engineers focus on designing and optimizing processes. Both roles require similar technical skills and certifications, but the manager role adds leadership and project oversight responsibilities.

How does a process engineer manager typically collaborate with cross-functional teams to implement process improvements?

A Process Engineer Manager often works closely with teams from production, quality assurance, maintenance, and supply chain to identify inefficiencies and develop solutions. This collaboration involves leading meetings to gather input, aligning on project goals, and ensuring all stakeholders are informed throughout the implementation process. The manager also facilitates training sessions for staff on new procedures and monitors the impact of changes, making adjustments as needed. Effective communication and leadership are essential to foster teamwork and drive successful process improvements.

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

To thrive as a Process Engineer Manager, you need a strong background in process engineering, project management, and a relevant engineering degree, often supported by experience in manufacturing or industrial settings. Familiarity with Lean Six Sigma methodologies, process simulation software, and ERP systems is typically required, and certifications like PMP or Six Sigma Black Belt are advantageous. Excellent leadership, problem-solving, and communication skills help you effectively manage teams and drive process improvements. These skills ensure efficient operations, cost savings, and the successful implementation of process enhancements across the organization.

What are the most commonly searched types of Process Engineer jobs in Saint Louis, MO?

The most popular types of Process Engineer jobs in Saint Louis, MO are:

What are popular job titles related to Process Engineer Manager jobs in Saint Louis, MO?

For Process Engineer Manager jobs in Saint Louis, MO, the most frequently searched job titles are:

What job categories do people searching Process Engineer Manager jobs in Saint Louis, MO look for?

The top searched job categories for Process Engineer Manager jobs in Saint Louis, MO are:

What cities near Saint Louis, MO are hiring for Process Engineer Manager jobs?

Cities near Saint Louis, MO with the most Process Engineer Manager job openings:

Process Engineer Manager jobs near you
Infographic showing various Process Engineer Manager job openings in Saint Louis, MO as of August 2026, with employment types broken down into 1% As Needed, 63% Full Time, 32% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $89,462 per year, or $43 per hour.

Process Engineer

Kindeva Drug Delivery

Brentwood, MO • On-site

Full-time

Re-posted 26 days ago

Job description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
This is an exciting opportunity as a Process Engineer that will serve as a technical leader and subject matter expert (SME) that is responsible for the design, implementation, optimization, troubleshooting, and lifecycle management of aseptic manufacturing processes and equipment used in the production of sterile pharmaceutical and/or biopharmaceutical products. This role provides strategic engineering support to ensure reliable, compliant, and high-performance aseptic manufacturing processes for injectable drug products (vials, syringes, cartridges, etc.). The engineer drives process optimization, contamination control, equipment lifecycle management, and continuous improvement while maintaining full compliance with cGMP, FDA, EMA, ISO, and other regulatory requirements.
Key Responsibilities
  • Act as the primary SME for aseptic manufacturing equipment, utilities (WFI, clean steam, compressed gases), and fill-finish systems (vial washers, depyrogenation tunnels, isolators/RABS, filling lines, cappers, lyophilizers, robotic systems, etc.).
  • Provide technical leadership for aseptic fill/finish operations, including process design, scale-up, process validation, troubleshooting, and ongoing performance monitoring.
  • Ensure robust aseptic practices and contamination control strategies (CCS) are implemented and sustained across all sterile operations.
  • Lead or support equipment and process lifecycle activities, including design reviews, FAT/SAT, IQ/OQ, requalification, and decommissioning.
  • Author, review, and approve technical documents such as SOPs, batch records, change controls, deviations, CAPAs, risk assessments, validation protocols/reports, and investigation reports.
  • Perform in-depth root cause analysis (using tools such as Fishbone, 5-Why, FMEA) on mechanical, automation, environmental and process deviations; author and implement CAPAs to drive permanent corrective solutions to improve yield, reduce downtime, and strengthen contamination control.
  • Drive process optimization and continuous improvement initiatives using Lean, Six Sigma, and data-driven approaches to increase yield, reduce cycle time, minimize interventions, and enhance sterility assurance.
  • Provide engineering oversight and troubleshooting support during manufacturing campaigns, including real-time shop-floor support for complex technical issues.
  • Collaborate with Quality Assurance, Validation, Microbiology, Regulatory, Supply Chain, Operations and MSAT teams to ensure successful tech transfers, new product introductions (NPI), and regulatory inspections.
  • Support regulatory submissions and inspections by preparing technical packages and defending aseptic processes.
  • Lead or significantly contribute to change controls, process improvement projects, and capital projects aimed at enhancing sterility assurance, throughput, and operational efficiency.
  • Author, review, and approve SOPs, batch records, preventive maintenance plans, calibration procedures, and engineering protocols/reports.
  • Support cleanroom performance qualification activities including airflow visualization (smoke studies), particle monitoring, pressure cascade management, and personnel/material flow optimization.
  • Mentor and provide technical guidance to junior engineers, manufacturing technicians, and cross-functional team members.
  • Monitor and analyze process performance metrics (e.g., yield, intervention rate, environmental monitoring trends, downtime) and implement improvements.

Qualifications & Requirements:
Education
  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Electrical Engineering, or a related technical discipline.

Experience
  • 1+ years of hands-on engineering experience in a cGMP regulated pharmaceutical, biopharmaceutical, or sterile medical device manufacturing environment.
  • Experience with isolator technology, RABS, vial/syringe/cartridge filling lines, lyophilization, aseptic connections, and closed-system processing.
  • Proven track record supporting sterile product manufacturing.

Preferred Technical Skills & Qualifications
  • Proficiency in mechanical design software: SolidWorks, AutoCAD Inventor, or equivalent (required: creation of complex 3D models, assemblies, detailed drawings, and tolerance analysis).
  • Automation knowledge: PLC programming (ladder logic, structured text), HMI/SCADA development, troubleshooting industrial control systems, and integration of robotic arms, servo systems, and vision technologies.
  • In-depth knowledge of aseptic fill-finish equipment: peristaltic/rotary piston pumps, vial/syringe/cartridge fillers, stoppering/capping systems, isolators/RABS, VHP decontamination, and barrier technologies.
  • Solid understanding of process control, instrumentation, sensors, actuators, and data acquisition systems.
  • Familiarity with data analytics tools (Excel, Minitab, JMP, OSIsoft PI) for process monitoring, capability analysis, and statistical evaluation.
  • Knowledge of cGMP requirements, EU Annex 1 contamination control strategy, sterility assurance, and cleanroom classification.
  • Experience executing or leading process/equipment validation, media fills, and cleaning validation in aseptic environments.
  • Exposure to lean manufacturing, Six Sigma, or reliability-centered maintenance methodologies.
  • Previous involvement in capital project execution or technology transfer projects.

What We Offer
  • Opportunity to take ownership of high-impact aseptic systems and automation projects.
  • Exposure to state-of-the-art fill-finish and barrier technologies.
  • Career development path toward Principal Engineer or technical leadership roles.
  • Competitive salary, bonus eligibility, and comprehensive benefits package.
  • Structured technical training and mentorship opportunities

#LI-Onsite
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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