Within this role you will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. You will provide engineering support and problem‑solving for existing equipment and manufacturing processes.
Typical Day
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 (P&IDs) and other related drawings.
Developing Process Flow Diagrams (PFDs) for manufacturing processes.
Supporting the QA Validation department by preparing design documents and assisting in protocol execution.
Reviewing and approving lifecycle documentation, cleaning validation protocols, and summary reports.
Assisting with investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents.
Assisting management with tracking of department throughput and efficiency.
Representing the engineering department at cross‑functional meetings.
Supervising direct reports as needed.
Implementing corrective/preventative actions for existing equipment and manufacturing processes.
Preparing engineering evaluations and test plans, and executing change control documentation.
Supervising mechanical, electrical, and automation contractors as needed.
Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations.
Maintaining company reputation by ensuring compliance with all relevant laws, policies, and regulations.
Qualifications
You have excellent technical and analytical skills.
You are skilled at problem‑solving and continuous improvement.
You possess strong communication and collaboration skills.
You are adaptable and can work in a fast‑paced, regulated environment.
To be considered for this opportunity you should have a B.S./B.Eng. or higher in chemical, process, or mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred; relevant experience may replace educational requirements.
Regeneron is an equal‑opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company’s business.
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