Within this role you'll be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment, providing engineering support and problem solving for existing equipment and manufacturing processes.A typical day might include, but is not limited to, the following:Designing and specifying cGMP process equipment, piping, and controlsManaging small-to-mid sized projects related to process equipment and manufacturingAssisting in the design review, site acceptance and installation of equipmentPreparing piping and instrumentation diagrams and other related drawingsDeveloping Process Flow Diagrams for manufacturing processesSupporting QA Validation department by preparation of design documents and assists in protocol executionAssisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidentsImplementing corrective/preventative actions for existing equipment and manufacturing processesPreparing engineering evaluations and test plans for change control documentationSupervising mechanical, electrical, and automation contractorsMaintaining a clean and safe working environment by enforcing procedures, policies, and regulationsMaintaining company reputation by enforcing compliance with all relevant laws, policies and regulationsThis role may be for you if:You possess excellent communication, negotiation, and stakeholder management skillsYou have the ability to think strategically and execute tactically in a fast-paced environmentYou are able to prioritise and re-prioritise as needed and adapt to changeTo be considered for this opportunity you should have a BS/BEng in Chemical, Process or Mechanical engineering with 8+ years related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.
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