Technical expert in Parenteral Technologies focusing on inspection equipment at a global healthcare leader. Partnering with sites to provide technical support and compliance in manufacturing operations.
Responsibilities
Partners with other technical staff to direct discipline activities
Ensure personal and team compliance with all applicable regulatory and corporate policy requirements
Assists sites globally with technical evaluations, master planning, technology assessments, and specific problem resolution
Provides ongoing technical support to site engineering groups, domestic and global.
Monitors and, when appropriate, influences change in external codes and standards on Lilly’s behalf.
Provides technical consulting and leadership to Lilly’s external manufacturing partners.
Requirements
Bachelor's degree in engineering or related technical field
Minimum 5+ years of experience in cGMP manufacturing or manufacturing support role
Extensive knowledge of parenteral visual inspection equipment (5+ years) and operations including automated, semi-automated and/or manual inspection equipment.
Qualified applicants must be authorized to work in the United States on a full-time basis.
Benefits
eligibility to participate in a company-sponsored 401(k)
pension
vacation benefits
eligibility for medical, dental, vision and prescription drug benefits
flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
life insurance and death benefits
certain time off and leave of absence benefits
well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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