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Open nowPosted 25 hours ago

Manufacturing Technician (Second Shift)

Kindeva Drug Delivery69 open roles

Where
Lexington, KY, USA
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Your applicationOpen nowManufacturing Technician (Second Shift)Kindeva Drug Delivery · Lexington, KY, USA

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Kindeva Drug Delivery's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. Kindeva Drug Delivery postings stay open a median of 20 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted 25 hours ago

Kindeva Drug Delivery median: 20 days open

The posting

Location: Lexington, KYShift: Second Shift | On-site Shift Schedule: 3:00 PM – 1:30 AM, Monday through Thursday and every other Friday 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! As a Manufacturing Technician, you will play a crucial role in supporting the manufacturing of life-changing and life-saving prescription nasal spray medications. Our Lexington facility continues to grow, creating opportunities to join our team, learn our processes, and develop your skills as we prepare for the future. Together, as One Team, we will manufacture more tomorrows! Responsibilities

Follow batch records to operate, monitor, and control equipment and process parameters during manufacturing. Complete training and follow Standard Operating Procedures (SOPs) to clean, sanitize, and prepare process equipment and production rooms for manufacturing. Accurately complete all required Good Manufacturing Practice (GMP) documentation. Maintain assigned manufacturing areas in accordance with 5S principles. Assist with training and onboarding other manufacturing team members. Assist with the execution of validation protocols for manufacturing and support equipment. Participate in routine preventive maintenance on facilities and equipment. Identify and escalate equipment or process issues affecting manufacturing operations. Recommend manufacturing process or facility improvements and cost-saving opportunities. Perform other duties as assigned by management.

Qualifications

High school diploma or GED. Minimum of 1 year of applicable experience in a GMP-regulated manufacturing environment. Pharmaceutical manufacturing experience preferred. Experience with sterilization processes or aseptic techniques preferred. Ability to follow SOPs and accurately complete GMP manufacturing documentation, including batch records and logbooks. Strong communication and interpersonal skills and the ability to work effectively in a team environment. Ability to meet applicable requirements for working with controlled substances.

Physical Requirements

Regularly use hands to handle materials and supplies. Use computers for extended periods each day. Communicate effectively by telephone and electronically. Stand and walk for extended periods of time. Occasionally lift and/or move up to 25 pounds. Use proper lifting techniques and remain aware of workplace hazards. Have adequate vision to read and execute documentation and perform job tasks compliantly and safely. Follow all site safety procedures.

Occupational Exposure / Risk Potential The work environment includes potential exposure to highly potent chemical compounds, hazardous materials, and toxic or controlled substances. Employees must adhere to stringent personal protective equipment (PPE) requirements, safe work methods, and established practices to ensure the safety and quality of personnel and finished products.

#LI-Onsite #WH

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