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Open nowPosted 402 days ago

Manufacturing Technician - 2nd Shift

kindeva78 open roles

Where
Lexington, KY, USA
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Your applicationOpen nowManufacturing Technician - 2nd Shiftkindeva · Lexington, KY, USA

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.6%1 day
  2. 3.4%3 days
  3. 7.8%7 days
  4. 14.3%14 days
  5. 33.7%30 days
This job: posted 402 days ago

The posting

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

  # LI-Onsite

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