Manufacturing Engineer

Kindeva Drug Delivery; Missouri; On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive base salary + performance bonus

Comprehensive benefits package

Structured mentorship programs

Job summary

Kindeva Drug Delivery is looking for a motivated Manufacturing Engineer in Missouri to support technical operations in Inspection, Assembly, and Packaging. This entry-level role is perfect for those wanting to build a career in pharmaceutical manufacturing, supporting equipment qualification, process optimization, and production data analysis.

You'll have the chance to work on high-speed automated inspection systems and participate in Lean initiatives while receiving structured mentorship.

Qualifications

• Bachelor’s degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, Biomedical Engineering, or a related technical discipline.
• 2+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environment.
• Exposure to Assembly, Inspection, or Packaging processes is preferred.

Responsibilities

• Support achievement of safety, quality, delivery, and cost objectives.
• Monitor and optimize assembly, inspection, labeling, and packaging processes.
• Collect and analyze production data to improve yield and throughput.

Skills

Analytical skills

Problem-solving skills

Familiarity with statistical tools

Basic understanding of cGMP principles

Education

Bachelor’s degree in Mechanical Engineering or related

Tools

Microsoft Office (Excel, Word, PowerPoint)

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 a motivated and detail‑oriented Manufacturing Engineer to support technical operations in our Inspection, Assembly & Packaging plant. This is a great opportunity for an entry‑level engineer looking to build a strong foundation in pharmaceutical manufacturing.

Key Responsibilities

• Support achievement of safety, quality, delivery, and cost objectives for operations.
• Support the monitoring and optimization of assembly, visual inspection, labeling, and packaging processes for vials, syringes, cartridges, and other pharmaceutical products.
• Assist in developing and updating process documentation, including SOPs, batch records, and process flow diagrams.
• Collect and analyze production data to identify opportunities for improving yield, throughput, and Overall Equipment Effectiveness (OEE).
• Participate in troubleshooting manufacturing issues related to automated packaging lines, vision systems, and serialization equipment.
• Assist in the execution of validation protocols (IQ/OQ/PQ, process validation) for inspection, assembly and packaging equipment.
• Support deviation investigations, CAPA implementation, and change control processes.LI>
• Help maintain equipment and processes in a validated state in accordance with cGMP, FDA, and EMA regulations.
• Participate in internal audits and prepare documentation for regulatory inspections.
• Collaborate with cross‑functional teams (Process Development, Quality Assurance, and Production) to ensure smooth scale‑up and successful product launches.
• Track actions, timelines, and deliverables to support project execution and site priorities.
• Support equipment qualification, preventive maintenance, and calibration activities.
• Work with senior engineers and maintenance teams to improve equipment reliability and uptime.
• Learn and support the operation of high‑speed automated inspection systems, assembly and packaging lines.
• Participate in Lean and continuous improvement initiatives (Kaizen events, 5S, etc.).
• Prepare technical reports and presentations as required.
• Support daily production floor activities and provide engineering support during manufacturing campaigns.

Qualifications & Requirements

• Bachelor’s degree in Mechanical Engineering, Chemical Engineering, Industrial Engineering, Biomedical Engineering, or a related technical discipline.
• 2+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environment (internships or co‑op experience in manufacturing is highly valued).
• Exposure to Assembly, Inspection, or Packaging processes is preferred but not required.
• Basic understanding of cGMP principles and pharmaceutical regulatory requirements.
• Strong analytical and problem‑solving skills.
• Familiarity with statistical tools, root cause analysis, and Microsoft Office (Excel, Word, PowerPoint).
• Ability to read and interpret technical drawings and equipment manuals is a plus.

Preferred Qualifications

• Internship or co‑op experience in pharmaceutical manufacturing or packaging operations.
• Knowledge of Lean Manufacturing or Six Sigma principles.
• Familiarity with automated inspection systems, serialization, or high‑speed packaging equipment.
• Experience working in a cleanroom or GMP environment.

What We Offer

• Competitive base salary + performance bonus
• Comprehensive benefits package (health, dental, vision, 401k, etc.)
• Structured mentorship and professional development programs
• Exposure to cutting‑edge pharmaceutical manufacturing technologies
• Clear career progression path toward Senior Manufacturing Engineer roles
• Collaborative and supportive work culture

California residents should review our Notice for California Employees and Applicants before applying.

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.