Senior Process Engineer

Kindeva Drug Delivery; Lexington (KY); On-site; USD 80,000 - 110,000; Full time

Job summary

An innovative pharmaceutical company is seeking a Senior Process Development Engineer to enhance the efficiency of life-saving nasal spray medications. In this pivotal role, you will drive process optimization, establish quality metrics, and lead training initiatives within a rapidly expanding facility. This position offers exceptional opportunities for professional growth while directly impacting patient care. If you're passionate about improving healthcare solutions and thrive in a collaborative environment, this is the perfect opportunity for you to make a difference.

Qualifications

• 7+ years of experience in process development within pharmaceutical manufacturing.
• Strong background in statistical methods and risk management.

Responsibilities

• Design and develop manufacturing processes for pharmaceutical production.
• Lead training initiatives for cleanroom operations.

Skills

Process Optimization

Statistical Methods

Risk Management

Technical Documentation

Education

Bachelor's Degree in Engineering

Master's Degree in Engineering

Tools

Statistical Analysis Software

Manufacturing Equipment

Job description

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

Why Kindeva?

• Collaborative team culture
• Direct impact on patient care

At Kindeva – Lexington, KY, we're not just making products – we're manufacturing life-saving nasal spray medications that make a difference.

The Impact You Will Make:

Join a rapidly expanding pharmaceutical CDMO where your work directly enhances the scalability and efficiency of life-changing treatments. As a Senior Process Development Engineer , you will drive process optimization by designing, testing, and deploying equipment and systems for pharmaceutical manufacturing. You will establish quality metrics, apply scientific and statistical methods to improve production, and solve complex processing challenges. With a high level of independence, you will serve as a technical specialist, supporting major production initiatives and potentially leading teams to ensure operational excellence.

Our Lexington facility is experiencing exponential growth, offering exceptional opportunities for professional development and advancement. Join us during this exciting expansion phase and grow your career while contributing to meaningful healthcare solutions.

Responsibilities:

• Design and develop manufacturing processes for routine pharmaceutical production.
• Draft batch records, protocols, and technical documents.
• Lead site-wide application of Risk Management and root-cause analysis tools, leveraging statistical methods
• Identify, qualify, and integrate new manufacturing equipment to enhance site capabilities.
• Serve as an industry resource, driving new technology adoption and product opportunities.
• Lead training initiatives for cleanroom operations in non-commercial manufacturing.
• Stay ahead of regulatory changes, ensuring seamless project execution from initiation to filing.
• Act as Lead Engineer in project teams and technical meeting with clients.

Qualifications:

• Looking for 7+ years of related experience

Join our One Team mission of manufacturing more tomorrows. Your expertise will help ensure better health and well-being for patients worldwide.

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!

• Job Family B - Engineering - Process Engineering