Manufacturing Technician - 2nd Shift

Kindeva Drug Delivery Company; Lexington (KY); On-site; USD 40,000 - 60,000; Full time

Job summary

Kindeva Drug Delivery Company is seeking a Manufacturing Technician in Lexington, Kentucky, to support the manufacturing of life-saving medications. In this role, you will operate equipment, maintain high standards of cleanliness, and participate in team efforts to improve patient outcomes.

Ideal candidates will have a high school diploma or GED with 0-5 years of experience in a pharmaceutical setting. This position emphasizes teamwork, communication skills, and adherence to safety protocols.

Qualifications

• 0-5 years of experience in pharmaceutical manufacturing environment.
• Experience with sterilization processes or aseptic technique preferred.
• Ability to write SOPs and other cGMP documents.

Responsibilities

• Operate and monitor production equipment.
• Clean and maintain manufacturing areas and equipment.
• Complete and review production documentation.

Skills

Attention to detail

Team collaboration

Written communication

Education

High School diploma or GED

Job description

Posted Thursday, January 15, 2026 at 5:00 AM

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

If you are ready to work for a purpose, join Kindeva Drug Delivery! Working on the KDD Manufacturing Team as a Manufacturing Technician, you will play a crucial role in supporting the manufacturing of life‑changing and life‑saving prescription nasal spray medications.

The Lexington location is experiencing exponential growth. Join our team, learn our processes and grow with our organization. Together, as One Team, we will manufacture more tomorrows!

Responsibilities

Responsibilities include cleaning, sanitizing, operating, and maintaining process equipment used to manufacture sterile nasal spray drug products and completing the associated documentation. By collaborating with cross‑functional teams, you’ll directly contribute to the improvement in patient outcomes around the world.

Key Manufacturing Duties

• Operate and monitor production equipment following PBRs and SOPs
• Clean and maintain manufacturing areas, equipment, and facilities
• Complete and review production documentation, including batch records and logbooks
• Train team members and coordinate with other departments
• Assist with validation protocols and improvement projects.
• Lead improvement projects and identify cost‑saving opportunities
• Ensure compliance with cGMPs, SOPs, and safety protocols

Qualifications

• High School diploma or GED.
• 0 – 5 years of applicable experience working in a pharmaceutical manufacturing environment.
• Experience with sterilization processes or aseptic technique preferred.
• Good written communication skills to write SOPs and other cGMP documents.
• Qualified to work with controlled substances.
• Strong interpersonal skills and the ability to work well in a team environment.

Physical Requirements

• Regular use of hands for documentation, equipment operation, and material handling
• Extended periods of standing and walking
• Ability to lift/move up to 60 pounds occasionally
• Full range of vision capabilities (close, distance, color, peripheral, depth)
• Must wear required PPE and follow cGMP/safety procedures
• Demonstrate proper lifting techniques and hazard awareness

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.

Job Family D - Quality - Manufacturing Quality Assurance