ZipRecruiter

Log In

1

Kindeva Jobs (NOW HIRING)

kindeva

Director of Engineering

Lexington, KY

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

kindeva

Senior CPR Project Manager

Bridgeton, MO

Why Kindeva? * Purpose-driven work environment * Significant growth potential * Collaborative team culture * Direct impact on patient care * Industry-leading innovation The Impact You Will Make: Join ...

Kindeva Drug Delivery

Financial Analyst

Woodbury, MN · On-site

$60K - $80K/yr

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 The Financial Analyst role will be ...

kindeva

Director of Engineering

Lexington, KY

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

kindeva

Senior CPR Project Manager

Bridgeton, MO

Why Kindeva? * Purpose-driven work environment * Significant growth potential * Collaborative team culture * Direct impact on patient care * Industry-leading innovation The Impact You Will Make: Join ...

Kindeva Drug Delivery

Process Engineer

Saint Louis, MO · On-site

Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our ...

kindeva

Senior CPR Project Manager

Bridgeton, MO

Why Kindeva? * Purpose-driven work environment * Significant growth potential * Collaborative team culture * Direct impact on patient care * Industry-leading innovation The Impact You Will Make: Join ...

Kindeva Drug Delivery

Senior Planner

Saint Louis, MO · On-site

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. Responsibilities * Generating an 18-month finished goods supply plan ...

kindeva

Senior CPR Project Manager

Bridgeton, MO · On-site

Why Kindeva? * Purpose-driven work environment * Significant growth potential * Collaborative team culture * Direct impact on patient care * Industry-leading innovation The Impact You Will Make: Join ...

Kindeva Drug Delivery

Manufacturing Engineer II

Lexington, KY · On-site

$72K - $93K/yr

Why Kindeva? * Purpose-driven work environment * Significant growth potential * Collaborative team culture * Direct impact on patient care * Industry-leading innovation At Kindeva - Lexington, KY, w ...

next page

Showing results 1-20

All JobsKindeva Jobs

Kindeva information

What is the difference between Kindeva vs Pharmacist?

AspectKindevaPharmacist
Required CredentialsTypically involves pharmaceutical manufacturing or research certificationsRequires a Doctor of Pharmacy (PharmD) degree and licensure
Work EnvironmentLaboratories, manufacturing plants, research facilitiesCommunity pharmacies, hospitals, clinics
Industry UsagePharmaceutical development, drug manufacturingDispensing medications, patient counseling

While Kindeva is involved in pharmaceutical manufacturing and research, pharmacists focus on dispensing medications and patient care. Both roles are integral to the pharmaceutical industry but differ in credentials, work environment, and daily responsibilities.

What are the key skills and qualifications needed to thrive as a Kindeva employee, and why are they important?

To thrive at Kindeva, you typically need a background in pharmaceutical sciences, chemistry, engineering, or related scientific fields, often supported by relevant degrees or experience. Familiarity with GMP regulations, pharmaceutical manufacturing equipment, and quality control systems is essential. Strong analytical thinking, teamwork, and effective communication skills help you excel in a collaborative and regulated environment. These competencies ensure the safe, efficient development and production of pharmaceutical products, meeting industry standards and patient needs.

What is Kindeva and what does the company do?

Kindeva is a global contract development and manufacturing organization (CDMO) specializing in drug delivery solutions, particularly inhalation, transdermal, and injectable products. They partner with pharmaceutical and biotechnology companies to develop, manufacture, and commercialize complex drug products. Kindeva offers services including formulation development, process scale-up, clinical manufacturing, and commercial production. Their expertise supports the advancement of innovative therapies for patients worldwide.

What types of projects and cross-functional teams can I expect to work with at Kindeva?

At Kindeva, employees often collaborate on multidisciplinary teams that include scientists, engineers, quality assurance specialists, and project managers. Project work typically involves developing and manufacturing drug delivery systems, so you'll have the opportunity to engage in innovative product development from concept through commercialization. This environment encourages frequent communication and knowledge sharing across departments, offering a dynamic setting for professional growth. Being part of these teams allows you to expand your expertise and build strong relationships across the organization.
What cities are hiring for Kindeva jobs? Cities with the most Kindeva job openings:
What states have the most Kindeva jobs? States with the most job openings for Kindeva jobs include:
Kindeva jobs near you
Infographic showing various Kindeva job openings in the United States as of May 2026, with employment types broken down into 85% Full Time, and 15% Nights. Highlights an 100% Physical job distribution.

Director of Engineering

kindeva

Lexington, KY

Other

Posted 17 days ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

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

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

As a Director of Engineering, you will lead Engineering, Maintenance, and Validation functions while also serving as the primary operations, portfolio, and business management point of contact for an assigned portfolio of clients and Kindeva’s Commercial/Business Development leadership. This role integrates technical leadership with client relationship management, ensuring operational excellence and client satisfaction

Responsibilities:

Engineering, Maintenance & Validation Leadership

  • Lead Engineering, Maintenance, and Validation teams in support of manufacturing operations.
  • Oversee plant commissioning, equipment procurement, and validation activities.
  • Ensure completion of equipment qualification and cleaning validation.
  • Maintain responsibility for the qualification and ongoing maintenance of production areas and equipment.

Client Portfolio & Business Integration

  • Lead Client Portfolio & Relationship Management actions and serve as the primary site operations point of contact to the client.
  • Ensure orchestrated client engagement models are established and executed.
  • Act as liaison with the Kindeva Commercial team and connect site functions with business development.
  • Champion operational engagement and provide leadership for client-facing routines and performance reviews.

People Leadership & Development

  • Develop and coach direct reports across engineering and client management functions.

 

Basic Qualifications:

  • Bachelor of Science (BS) degree in a science-related field, engineering, or equivalent experience.
  • BS/MS in Engineering or related field.
  • 10+ years in GMP manufacturing/engineering.
  • 3+ years in managing technical teams.
  • Hands-on experience in validation, equipment troubleshooting, and repair.
  • Strong understanding of client relationship management in a CDMO environment.
  • Excellent communication, leadership, and organizational skills.
  • Physical ability to work across office and manufacturing environments, lift/move up to 25 pounds, and follow safety protocols.

 

Preferred Qualifications:

  • M.B.A. preferred
  • 15+ years cGMP experience in biotech, pharmaceutical, or biopharmaceutical manufacturing environment, ideally pre-clinical phases through commercial, and/or equivalent amount of experience managing commercial operations or client portfolio management roles.
  • 5 years of experience with FDA/EU and participation in regulatory agency inspections, preferred.
  • Strong leadership, high level of personal/departmental accountability, and responsibility.

Physical Requirements:

  • Position requires the ability to sit and/or stand for extended periods and to work in a variety of settings, including office areas, manufacturing areas, and warehouse etc.
  • Must be able to walk to and access all work areas. Routinely climbing stairs is necessary.
  • Use of eye protection, gloves, and other PPE is required.

 

Non-Standard Work Schedule / Travel or Environment Requirements:

  • Position requires regular onsite attendance – responsibilities for this position cannot be performed on a remote or telecommute basis.
  • Must have the ability to simultaneously multi-task across multiple capabilities, functions, and manage competing priorities, including performing site and functional responsibilities, frequent e-mail and phone communications, and attending multiple meetings and conference calls. Note: these activities may not be time-bound to core hours or presence at the site.
  • Must have the ability to effectively manage strict production, time, and performance deadlines.
  • Must be willing and able to work beyond the hours typically defined as a “regular” workday, which may or may not include weekends and holidays.

 

#LI-Onsite

Apply