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Senior Robotics Engineer Localization Jobs in Missouri

kindeva

Senior Manufacturing Engineer

Maryland Heights, MO · On-site

$87K - $120K/yr

... systems, robotics, and serialization/track-and-trace systems. * Lead by example in safety ... at least 2 years in a Senior Engineer or equivalent role. * Strong experience in Assembly ...

kindeva

Senior Manufacturing Engineer

Maryland Heights, MO · On-site

$87K - $120K/yr

... systems, robotics, and serialization/track-and-trace systems. * Lead by example in safety ... at least 2 years in a Senior Engineer or equivalent role. * Strong experience in Assembly ...

kindeva

Senior Manufacturing Engineer

Maryland Heights, MO · On-site

$87K - $120K/yr

... systems, robotics, and serialization/track-and-trace systems. * Lead by example in safety ... at least 2 years in a Senior Engineer or equivalent role. * Strong experience in Assembly ...

kindeva

Senior Manufacturing Engineer

Maryland Heights, MO · On-site

$87K - $120K/yr

... systems, robotics, and serialization/track-and-trace systems. * Lead by example in safety ... at least 2 years in a Senior Engineer or equivalent role. * Strong experience in Assembly ...

Motivo

Senior Electrical Engineer

California, MO · On-site

$110K - $130K/yr

Our work spans a wide range of market segments, including mobility/automotive, aerospace, robotics ... We are looking for an enthusiastic Senior Electrical Engineer who enjoys being part of a tight-knit ...

Spartech

Senior Process Engineer (REQ865)

Saint Louis, MO · On-site +1

$98K - $127K/yr

Senior Process Engineer Maryland Heights, MO Spartech offers a competitive salary, incentives, and ... robotics, and secondary operations. Equipment Procurement & Vendor Management * Develop RFQs ...

BioRobotics

Senior Equipment Engineer

California, MO · On-site

$93K - $128K/yr

... robotics. As our company succeeds and grows, we improve the quality of life of patients, provide ... Senior Equipment Engineer,** you will bring your hands on expertise to develop new equipment ...

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Senior Robotics Engineer Localization information

What is the difference between Senior Robotics Engineer Localization vs Robotics Software Engineer?

AspectSenior Robotics Engineer LocalizationRobotics Software Engineer
Required CredentialsBachelor's or Master's in Robotics, Computer Science, or related; experience in localization algorithmsBachelor's or Master's in Computer Science, Software Engineering, or related; programming skills
Work EnvironmentRobotics development labs, field testing, autonomous vehicle companiesSoftware development teams, robotics companies, research labs
Industry UsageAutonomous vehicles, mobile robots, dronesRobotics applications across industries, including manufacturing and service robots

While both roles involve robotics software development, Senior Robotics Engineer Localization specializes in developing algorithms for determining a robot's position within its environment, often requiring expertise in sensor fusion and mapping. Robotics Software Engineers focus broadly on creating software for robot control, perception, and navigation. The localization role is more specialized, whereas the software engineer role covers a wider range of robotics software development tasks.

What are the most commonly searched types of Robotics Engineer Localization jobs in Missouri?

The most popular types of Robotics Engineer Localization jobs in Missouri are:

What cities in Missouri are hiring for Senior Robotics Engineer Localization jobs?

Cities in Missouri with the most Senior Robotics Engineer Localization job openings:

Senior Robotics Engineer Localization jobs near you

Senior Manufacturing Engineer

Maryland Heights, MO • On-site

Kindeva Drug Delivery
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees
Learn more about Kindeva Drug Deliveryexternal

$87K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 27 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
We are seeking an experienced Senior Manufacturing Engineer to lead technical operations and process optimization in our state-of-the-art Assembly, Inspection, and Packaging plant. In this critical role, you will drive manufacturing excellence for pharmaceutical products (sterile and non-sterile) while ensuring full compliance with cGMP, FDA, EMA, and other regulatory requirements.
As a senior technical leader, you will be responsible for equipment performance, process robustness, continuous improvement, new product introductions (NPI), Tech Transfers in high-speed automated inspection, assembly and packaging lines.
Key Responsibilities
  • Lead the design, qualification, and optimization of visual inspection, assembly, labeling, and packaging processes for vials, syringes, cartridges, auto-injectors, and other pharmaceutical delivery devices.
  • Develop and maintain process flow diagrams, equipment specifications, and critical process parameters (CPPs).
  • Identify and implement process improvements using Lean, Six Sigma, and data-driven methodologies to increase throughput, yield, and equipment effectiveness (OEE).
  • Lead capital and continuous improvement projects from concept through implementation, including scope definition, URS development, vendor engagement, FAT/SAT support, commissioning, qualification, and handoff to operations.
  • Troubleshoot complex manufacturing issues related to high-speed automation, vision systems, robotics, and serialization/track-and-trace systems.
  • Lead by example in safety, environmental, and compliance practices; identify and mitigate operational risks in manufacturing processes and equipment.
  • Author, execute, and review validation protocols (IQ/OQ/PQ, process validation, and computer system validation) for new and existing equipment.
  • Ensure all manufacturing processes remain in a validated state and comply with 21 CFR Parts 210/211, Annex 1, and ISO standards.
  • Support regulatory inspections (FDA, EMA, etc.) and internal audits as a subject matter expert (SME) for IAP processes.
  • Lead deviation investigations, CAPA implementation, and change control activities.
  • Serve as the primary manufacturing engineering lead for technology transfers and scale-up of new products into the IAP plant.
  • Collaborate with Process Development, Quality Assurance, and Regulatory Affairs to ensure manufacturability and compliance.
  • Support design for manufacturability (DFM) reviews during product development.
  • Evaluate, select, and implement new assembly, packaging and inspection technologies (e.g., automated visual inspection systems, high-speed labelers, cartoners, case packers).
  • Manage equipment reliability programs, including preventive maintenance optimization and spare parts strategy.
  • Work closely with Reliability, Maintenance and Automation Engineering teams on equipment uptime and performance.
  • Mentor and provide technical guidance to junior Manufacturing Engineers and technicians.
  • Lead cross-functional teams on major projects and Kaizen events.
  • Drive OEE improvement initiatives and cost reduction programs.
  • Prepare technical reports, presentations, and documentation for leadership and clients

Qualifications & Requirements
  • Bachelor's degree in Mechanical, Chemical, or Industrial Engineering, or a related technical field; master's degree preferred.
  • Minimum 6+ years of experience in pharmaceutical or biotechnology manufacturing, with at least 2 years in a Senior Engineer or equivalent role.
  • Strong experience in Assembly, Inspection, and Packaging of sterile injectables or complex drug-device combination products is required.
  • Proven track record with high-speed automated packaging lines, vision inspection systems, and serialization systems.
  • Deep knowledge of cGMP, validation principles (GAMP 5 - Risk Based approach to compliant GxP design and systems), and pharmaceutical regulatory requirements.
  • Experience with statistical process control (SPC), Design of Experiments (DOE), and root cause analysis tools (FMEA, Fishbone, etc.).
  • Proficiency in reading technical drawings (P&ID, mechanical layouts) and working with CAD software.
  • Familiarity with Track-and-Trace, 2D coding, and anti-counterfeiting technologies.
  • Lean Six Sigma Green Belt or Black Belt certification is highly desirable.
  • Strong leadership and project management skills.
  • Excellent technical writing and communication abilities.
  • Ability to thrive in a fast-paced, client-focused CDMO environment.

Preferred Qualifications
  • Experience supporting commercial manufacturing for large pharmaceutical clients.
  • Knowledge with integrated packaging systems such as feeders, labelers, cartoners, checkweighers, case packers, reject systems, vision inspection, and serialization/aggregation platforms preferred.Previous experience in a multi-product CDMO facility.
  • Project management certification (PMP) or equivalent.

What We Offer
  • Competitive base salary + performance bonus
  • Comprehensive benefits package (health, dental, vision, 401k, etc.)
  • Professional development and conference opportunities
  • Exposure to cutting-edge pharmaceutical manufacturing technologies
  • Collaborative and innovative work culture

#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.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

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