MSAT Process Engineer/Scientist III - Downstream

MSAT Process Engineer/Scientist III – Downstream Location: On-site, Portsmouth, NH.   The MSAT Engineer/Scientist III is responsible for being the primary technical support for mammalian manufacturing processes. This person has in-depth experience with supporting manufacturing processes and/or technical transfer. The supervisor provides direction and oversight, as this level of Process Engineer/Scientist is expected to have a good grasp of the requirements of the role. The individual is a subject matter expert for key aspects of the role, and it is expected that questions on tasks or issues will be raised by this individual when clarification or greater technical expertise is required. What you will get: Competitive salary and comprehensive benefits package. Opportunities for career development and advancement. Supportive and collaborative team environment. Access to cutting-edge technology and tools. Commitment to employee well-being and safety. Inclusive workplace culture. Recognition and reward for your contributions. Access to our full list of global benefits:  https://www.lonza.com/careers/benefits What you will do: Performs all functions associated with process transfer and process support, e.g. develop process understanding, perform gap analysis/FMEA, generate process models, author / review Process Descriptions and Batch Records, author/review planned deviations and change controls, perform process monitoring author campaign summary reports, perform activities for lot release. May provide guidance on process transfer and support activities to junior members of the team. Assess all major deviations including those that impact product quality and identify potential root causes using a systematic approach.  Experience using variety of problem solving tools e.g. Fishbone, Kepner-Tregoe etc. Able to identify potential solutions.  Performs or is able to understand all types of complex data analysis such as multiple linear regression analysis, ANOVA, multivariate analysis. Author and review process descriptions, definitive formulations, batch records, raw material listings, change controls independently and authors/reviews/modifies the corresponding templates.  Assess change controls for impact of any change to the process, equipment or procedures that can affect process performance and product quality. Supports documentation preparation for regulatory purposes. Represent MSAT on project teams and interfaces with customer technical and quality representatives. Represent MSAT on internal teams (e.g. Deviation and Run Daily Management System meetings).  Participate in Customer and Regulatory Audits. What we are looking for: Bachelor’s degree in Biotechnology, Biological Sciences, or Chemical Engineering. 5+ years of biotech industry experience (3+ years with Master’s, 2+ years with PhD) in process development and process scale up / manufacturing.  Experience with large scale manufacturing…