Job Description:
This role involves designing, specifying, and commissioning new and renovated biopharmaceutical process equipment.
Responsibilities include providing engineering support and problem-solving for existing equipment and manufacturing processes.
A typical day may involve:
* 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 assisting 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 requires excellent communication, negotiation, and stakeholder management skills.
Candidates should have a BS/BEng in Chemical, Process, or Mechanical Engineering with 8+ years of related experience.
Direct experience with biopharmaceutical process equipment is preferred.
Regeneron is an equal opportunity employer and provides comprehensive benefits, including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels.