Manufacturing Operator
Listed on 2026-01-25
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Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing Production, Operations Engineer
Division Overview
Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10 year history of extraordinary manufacturing practices in the solid oral dose arena. The support and expertise of our parent organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly.
The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations under manufacture, we have a robust pipeline of products. Aurolife's aim is to provide healthcare at economical prices to make this a healthier world to live in.
Manufacturing Operator is to perform all required Batch manufacturing, packing, equipment cleaning, area cleaning, in-process testing & sampling for Manufacturing and Packaging batches. Perform maintenance and troubleshooting of the equipment and machinery. Perform verifications using special instruments (Caliper, Balance, etc.)
Responsibilities- Assist the Batch manufacturing, Packing & Cleaning of the equipment machinery and area.
- Assist all required in-process testing & sampling of batches in progress and products to be packaged.
- Assist Calibration of weighing and required equipment.
- Perform packaging activities.
- Perform other duties as assigned.
- Handle various requests from departments for developmental or investigative reasons.
- Complete all applicable training forms in a timely manner.
- Troubleshooting the manufacturing equipment as needed.
- Perform dispensing activity as needed.
- Experienced with Metered dose inhaler (MDIs) production environment.
- Familiar with proper documentation and correction practices.
- Must be a Team player.
- Be able to effectively communicate with Supervisor, IPQA, Quality Control, Production, Warehouse and Engineering.
- Possess the ability to analyze information and make consistently good decisions.
- High School Diploma with some college courses, Associates Degree.
- 1+ year experience performing Batch Manufacturing and Packing, In-process checks/verifications in the Manufacturing and Packaging areas of pharmaceuticals manufacturing environment.
- A familiarity with cGMPS, CFRs, OSHA and FDA regulations.
- Knowledge of deviations/incidents and CAPA.
WAREHOUSE OR PRODUCTION POSITION – While performing the duties of this job the employee is required to:
Regularly lift and/or move objects 10-50lbs Frequently required to stand, walk, stoop, kneel, crouch or crawl Occasionally required to sit and climb or balance Specific vision abilities required for this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust and focus The worker is subject to environmental conditions. Protection from weather conditions but not necessarily from temperature changes The worker is subject to both environmental conditions.
Activities occur inside and outside Medium work Exerting up to 50 pounds of force occasionally, and/or up to 30 pounds of force frequently, and/or up 10 pounds of force constantly to move objects.
Physical Requirements Blood/Fluid Exposure Risk
Category III:
Tasks involve no exposure to blood, body fluids or tissues. Category I tasks are not a condition of employment.
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