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Employment Opportunities |
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The following openings are currently available.
To view a complete job description, please click on the position title.
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May 2009: Validation Engineer
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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.
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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). |
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If you would like to apply for a position with Gala
Biotech, please send your cover letter, resume, and salary requirements. |
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by mail: |
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Human Resources
Gala Biotech
PO Box 620160
Middleton, WI 53562
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by e-mail: |
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gala.hr@catalent.com |
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Click here
for driving directions to Gala Biotech |
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