Manufacturing Technician - Third Shift

ZipRecruiter; Lexington (KY); On-site; USD 30,000 - 50,000; Full time

Job summary

Join a leading company in the pharmaceutical sector as a Manufacturing Technician in Lexington, KY. Contributing to the production of life-saving nasal spray medications, you'll be responsible for equipment operation, documentation, and maintaining production integrity. The role offers growth opportunities in a thriving environment focused on improving patient outcomes.

Qualifications

• 0 - 5 years of applicable experience in pharmaceutical manufacturing.
• 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.

Skills

Written communication skills

Interpersonal skills

Education

High School diploma or GED

Job description

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:

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 improving 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.

# LI-Onsite

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

Equal Opportunity Employer:

Kindeva Drug Delivery is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other basis covered by applicable federal, state, and local laws. Employment decisions are based on qualifications, merit, and business needs.