Manufacturing Technician - First Shift

ZipRecruiter; Lexington (KY); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading company in drug delivery is seeking a Manufacturing Technician in Lexington. The role involves supporting the production of life-saving nasal medications, ensuring compliance with safety standards, while collaborating with cross-functional teams to improve patient outcomes. Ideal candidates should have a high school diploma and relevant experience in a pharmaceutical setting.

Qualifications

• 0 - 5 years of applicable experience in a pharmaceutical manufacturing environment.
• Experience with sterilization processes or aseptic technique.
• Qualified to work with controlled substances.

Responsibilities

• 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.

Skills

Written Communication

Interpersonal Skills

Education

High School diploma or GED

Job description

Job DescriptionJob 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:

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 .
• 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, , peripheral, depth)
• Must wear required PPE and follow cGMP/safety procedures
• Demonstrate proper lifting techniques and hazard awareness

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