Granulation & Blending Operator II

Aurolife was founded in 2008 as part of a group of companies that has a long history of excelling in generic pharmaceutical prouct 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.

It is the Granulation & Blending Operator II’s responsibility to ensure that the equipment’s used for e.g. Mechanical Sifter, Granulator, Fluid Bed Dryer, Fitz Mill, and blenders are clean and set up properly.  It is the operator’s responsibility to perform visual and physical checks of in-process and finished materials as per procedure of Production Batch Record.

• Clean and/or disassemble the equipment e.g. Mechanical Sifter, Granulator, Fluid Bed Dryer, Fitz Mill, Blender after the completion of product run as per SOP.
• Clean manufacturing room after the completion of product run as per SOP.
• Set up equipment as per Sop’s, and as per specifications in Production Batch Record.
• Maintain equipment in good working order, inspect equipment for wear and tear, and have any worn or evaluate malfunctioning parts and report to Production Supervisor or Manager.
• Maintain equipment parts and supplies in proper condition.
• Make any machine adjustments necessary during the batch run as required.
• Document all set up and cleaning in the log book and other pertinent paperwork.
• Visually inspect equipment as it is running to verify the machine is running within normal and safe operation.
• Take in process measurements of during the product run, and document these measurements in Production Batch Record.
• Keep the equipment and room clean during the production.
• Make sure all paperwork is complete and accurate throughout and after production.
• Keep accurate records of equipment usage and inspections.
• Perform any and all additional tasks relating to the operation of the manufacturing department as requested.
• Follow company policies, cGMP’s and Standard Operating Procedures.
• Other misc. duties as assigned.

• A demonstrated ability to follow written instructions precisely and perform basic math calculations is required.
• Should have an understanding/knowledge of cGMP, safety criteria or the ability to learn.

• High School Graduate.
• Up to one (1) year of work experience in a pharmaceutical manufacturing environment.