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 controls
* Managing small-to-mid sized projects related to process equipment and manufacturing
* Assisting in the design review, site acceptance and installation of equipment
* Preparing piping and instrumentation diagrams and other related drawings
* Developing Process Flow Diagrams for manufacturing processes
* Supporting QA Validation department by preparation of design documents and assists in protocol execution
* Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents
* Implementing corrective/preventative actions for existing equipment and manufacturing processes
* Preparing engineering evaluations and test plans for change control documentation
* Supervising mechanical, electrical, and automation contractors
* Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations
* Maintaining company reputation by enforcing compliance with all relevant laws, policies and regulations
This role may be for you if:
* You possess excellent communication, negotiation, and stakeholder management skills
* You have the ability to think strategically and execute tactically in a fast-paced environment
* You are able to prioritise and re-prioritise as needed and adapt to change
To 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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