Job Role: Industrial Engineer II 

Overview: 

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com

Our Fortune 500 Medical Device client has an exciting opportunity for Industrial Engineer II. 

Job Summary:  

The Industrial Engineer II will provide support for new building site transfer activities to achieve project and production goals (i.e., safety, quality, delivery, cost, and productivity). 

Responsibilities and Job Requirements:  

• Optimize process flow and facility layout for material handling and production using lean principles. 

• Analyze the specifications and requirements of the line design modifications and adjust layout plan accordingly. 

• Complete time studies, standard times and labor calculations, and estimate savings to measure impact of process and layout changes. 

• Develop capacity planning tools and production models to quantify impact of process and layout changes. 

• Execute for operational readiness including 5S, production area signage, material flow, and safety and quality requirements. 

• Develop site signage to global branding standards. 

• Apply project management skills (scope, schedule, cost) and collaboration with cross-functional partners to execute projects in a timely and cost-effective manner. 

• Proficiency in various layout design and development software tools and programs, such as AutoCAD, DraftSight, and Microsoft Products Suite. 

Quality Systems Duties and Responsibilities: 

Build Quality into all aspects of their work by maintaining compliance to all quality requirements 

Qualifications 

• Bachelor’s Degree or equivalent in Industrial Engineering or similar 

• Minimum 2 years' proven experience. Anything under 2years will be DQ'd. 

• Must have proficiency in layout design & development software tools & programs (such as, AutoCAD, DrafSight and Microsoft Products Suite). 

• Must have a 'quality' mindset, detailed, and collaborative. 

• Project management skills. 

Preferred Qualifications: 

• Lean manufacturing and process improvement experience 

• Facility layout and design 

• Medical device industry experience 

Other Details: 

• 6-month Contract 
• Full Time - (08:00:AM - 04:30:PM)
• On-site at Alpharetta, GA 30009 

EEO Employer:  

Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com. 

Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.