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Product Development - Solid Dosage Formulator

 

Job ID

2013-19430

# Positions

1

Location

US-SC-Greenville

Posted Date

10/18/2013

Category

Product Development

Job ID

2013-19430

# Positions

1

Location

US-SC-Greenville

Posted Date

10/18/2013

Category

Product Development

More information about this job:

More information about this job:

Job Summary:

Job Summary:

Responsible for formulating and supporting solid dose product formulations from the prototype stage through the production stage.

Responsible for formulating and supporting solid dose product formulations from the prototype stage through the production stage.

Essential Duties and Responsibilities:

Essential Duties and Responsibilities:

Essential Job Functions

  • Develop new and reformulate existing products to meet customer requirement (Tablets/Hardshell Capsules).
  • Cost formulas for new and revised products.
  • Prepare and approve Master Batch Records (MBR’s), Master Change Requests (MCR’s), Formula A-Pages.
  • Provide Technical support to SD Manufacturing and Operations and monitor initial production batches of new product formulations.
  • Perform/assist with special or non-routine project assignments.

Non-Essential Job Functions

  • Maintain required records, such as laboratory notebooks and computer logs. Perform special projects as assigned.
  • General knowledge of cGMP’s, SOP’s and knowledge of FDA and OSHA regulations. Generate finished product costing.

Essential Job Functions

  • Develop new and reformulate existing products to meet customer requirement (Tablets/Hardshell Capsules).
  • Cost formulas for new and revised products.
  • Prepare and approve Master Batch Records (MBR’s), Master Change Requests (MCR’s), Formula A-Pages.
  • Provide Technical support to SD Manufacturing and Operations and monitor initial production batches of new product formulations.
  • Perform/assist with special or non-routine project assignments.

Non-Essential Job Functions

  • Maintain required records, such as laboratory notebooks and computer logs. Perform special projects as assigned.
  • General knowledge of cGMP’s, SOP’s and knowledge of FDA and OSHA regulations. Generate finished product costing.

Job Specifications:

 

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