Employment Opportunities
   
  The following openings are currently available. To view a complete job description, please click on the position title.
   
 
May 2009: Validation Engineer  PDF page_white_acrobat (1K)   HTML html (1K)
   
  The Operations Department is responsible for materials management, which includes warehousing and control of material movement, calibration and validation activities, and cGMP activities. cGMP manufacturing includes cell banking, upstream (cell culture) and downstream (protein purification) activities.

The Validation Engineer has the primary responsibility for protocol development and execution of validation qualifications. Where applicable, oversight of contractor validation may be necessary. The Validation Engineer will conduct validation activities, based upon engineering specifications that include authoring and editing protocols, executing validation protocols and writing reports. The Validation Engineer will identify deviations from test plan and will work with functional groups to resolve deviations.
   
   
   
  Gala Biotech, a Catalent Pharma Solutions Company, is an exciting and growing organization. We offer a competitive salary and benefits package, including comprehensive health, life and disability insurance, and 401(k).
   
  If you would like to apply for a position with Gala Biotech, please send your cover letter, resume, and salary requirements.
   
 
by mail: Human Resources
Gala Biotech
PO Box 620160
Middleton, WI 53562
  by e-mail:   gala.hr@catalent.com
   
  Click here for driving directions to Gala Biotech
 
 
 
 
 
 
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