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Process Engineer II-Framingham, MA

Sanofi

This is a Contract position in Framingham, MA posted June 12, 2019.

Process Engineer II-Framingham, MAPosition: Process Engineer II, Upstream Pilot LabDEPARTMENT DESCRIPTION:The Process Engineer (PE) II position is part of Process Science in Global Manufacturing Science & Technology (MSAT) Pilot Lab and is based at the biologics hub in Framingham, MA.

The Global MSAT function assures robustness and economics of cell-culture based manufacturing processes in support of life cycle management (LCM) of biological proteins expressed from mammalian systems by:Driving next generation LCM process development & supporting key strategic initiativesLeading technology transfer, scale-up development & adaptation, process automation, process control strategy, process validation, and comparability at Sanofi and external industrial sitesProviding technical assistance for commercial manufacturing at Sanofi & external sites including change assessment, process monitoring, troubleshooting, and continuous process improvementPosition overview /Key responsibilities:The PE II will be a key contributor in the Process Science Upstream Pilot Lab group.

The successful candidate will apply scientific and engineering principles and utilize cell culture, bioreactor, and separation technologies to: improve current commercial and develop next-generation processes of monoclonal antibodies and recombinant proteins, with responsibilities spanning bench and pilot-scale process development & characterization, as well as support of technology transfer to manufacturing facilities.

This individual will work in a team environment, collaborating with various colleagues in the organization to solve a wide range of complex problems in creative and practical ways.

Specific Responsibilities include:Work collaboratively within the MSAT group to execute and participate in the design of Pilot scale operations; contributes to data analysis and interpretation of resultsSet-up and maintain upstream Pilot laboratory equipment, systems, and trainingAuthor internal procedures and technical reportsPresent data and results within department and project teamsMay contribute/ lead small project teams for technology transfer to manufacturingKey responsibilities may differ among employees and change over time, in accordance with business needsBasic qualifications:Bachelor’s degree in chemical engineering, biology, biochemistry or equivalent with 4 years of professional experience, or MS with 2 years.Preferred qualifications:MS degree with at least 2 years professional cell culture experience in chemical engineering, biology, biochemistry or equivalentExperience in biotechnology or pharmaceutical industryHands-on experience at laboratory, pilot, or manufacturing scale for biologics productsKnowledge in cell culture process development, bioreactor design and control strategies, scale up and scale down as applied to mammalian-expressed proteinsExcellent scientific backgroundHighly motivated individual with the ability to work independently and on cross-functional and cross-site teamsStrong technical writing and presentation skillsExperience with statistical analysis softwareLEADERSHIP QUALIFICATIONS: Strives for results: sets ambitious tangible and measurable targets; takes personal responsibility for achieving results; reviews and evaluates progress against agreed targets, timelines and budgetsCooperates transversally: Shares information and seeks input from outside direct team.

Develops strong cross functional relationships and partnerships with science and commercial organizationCommit to customers: Shares relevant information openly and seeks appropriate input from others outside of the direct team; develops and maintains effective cross-functional working relationships and partnerships; responds positively and constructively to requests for support from across the organizationAct for Change: Creatively challenges the status quo to find new ways of working; looks for the opportunities that arise during times of change; readily adapts to new environment, jobs, technologies and processes.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-SGLI-GZAt 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.Sanofi is dedicated to supporting people through their health challenges.

We are a global biopharmaceutical company focused on human health.

We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering.

We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.Sanofi, Empowering Life