Engineer Principal-Framingham, MA

Job description

Key Responsibilities:

·  Ensure internal customers are provided with the right technical solution within process discipline
·  Inspire internal customers by providing innovative solutions/options for project feasibility and conceptual design
·  Development of technical solutions around operational & business goals
·  Implement Global Biologics Engineering design standards
·  Conduct reviews of risks and facilitate implementation of design approaches to mitigate those risks
·  Use specialist (SME) knowledge and experience to solve complex tasks around drug substance manufacturing operations
·  Develop and implement tools for risk assessment and early-phase project execution framework
·  Deliver on-the-job knowledge sharing/training/mentoring within DTS
·  Follow Industry technology trends and maintain knowledge within key technical disciplines
·  Convey and share knowledge within DTS
·  Review and assess lessons learned from projects, recommend improvements of tools/methods and give input to implementation
·  Review compliance aspects of process design against global regulatory standards, focused on CPPs
·  Support development of new methods/tools/ for Process design execution and improve existing solutions supporting an operational approach
·  Be engaged in local professional network

BASIC QUALIFICATIONS:

·  B.S or M.S. degree in process engineering discipline
·  Minimum 10 + years of experience in bio-manufacturing design/consulting

PREFERRED QUALIFICATIONS

·  Recognized expert within process discipline and Subject Matter Expert in the technical competencies within the process discipline
·  Knowledge of both stainless steel and single-use manufacturing equipment platforms
·  Knowledge of the life-cycle requirements for bio-manufacturing process development, plant design, tech transfer, and start-up
·  Experience in multi-product plant design in biologics
·  Act as a technical leader who sets standards within the GBE and supports knowledge transfer globally
·  Keep close contact with the market and internal customers to spot current/future requirements (trends)
·  Be passionate about technical discipline and eager to develop ideas and spread the message
·  Be adept at finding better methods and solutions for our internal customer/project requirements
·  Participate actively in global site needs
·  Experience in the execution (design, build, start-up) of capex projects for drug substance manufacturing
·  Experience and comfort working in complex corporate environment

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

#GD-SG

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.