Mechanical Engineer - Madison, WI | Biospace
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Mechanical Engineer

Catalent Pharma Solutions, Inc.

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Location:
Madison, WI
Posted Date:
5/18/2017
Position Type:
Full time
Job Code:
0021472
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:
Engineering,

Job Description


About Catalent

Catalent Pharma Solutions is the leading global provider of advanced delivery technologies and development solutions for drugs, biologics and consumer health products.  With over 80 years serving the industry, Catalent has proven expertise in bringing more customer products to market faster, enhancing product performance and ensuring reliable clinical and commercial product supply. Catalent is headquartered in Somerset, N.J. For more information, visit www.catalent.com
                                             
More products. Better treatments. Reliably supplied.™

Job Duties:                                                                                        

-   Supports the multi-use facility, including HVAC systems and bio-containment systems.
-   Supports selection and installation of manufacturing equipment.
-   Proactively and effectively partners with the facility commissioning/validation team, including operational protocol development, to implement compliance with FDA GMP requirements.
-   Drafts Standard Operating Procedures for building operation, maintenance and calibration.
-   Identifies improvements and efficiencies of facility preventative maintenance.
-   Provides engineering guidance and execution on facilities and equipment projects.
-   Performs hands-on activities as needed to help trouble shoot facility problems and support facility staff.
-   Develops standard processes to evaluate future capital projects.
-   Drives continuity and development of standards in Project Engineering to ensure smooth and effective communication flow between internal resources and customers, operational efficiency, and equipment and personnel safety.
-   Creates and maintains all aspects of equipment design files.
-   Maintains project compliance in accordance with the site quality management system.
-   Guides the specification and selection of manufacturing / utility equipment to support site facility / process needs.
-   Other duties as assigned.

Requirements


Education:

-   Minimum B.S. degree with concentrated studies in Engineering or Science.
 
Experience:

-   Minimum 3 years’ facilities operation/engineering experience in a cGMP environment (preferably biopharmaceutical)