We are looking for an experienced Project Engineer to join our growing Engineering team. Our Project Engineers design, specify and commission new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.
As a Principal Project Manager - Engineering, a typical day might include the following:
- Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation
- Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning
- Assisting in and leading 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 preparing 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 and executing modification change control documentation
- Supervising mechanical, electrical, and automation contractors
- Traveling up to 25% of the time, both domestically and internationally
This position might be for you if you:
- Have working knowledge of biopharmaceutical equipment, including filling, device assembly, label, and packaging equipment
- Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes
- Enjoy solving puzzles and challenges, supporting investigations across the business
- Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment
- Want to do more than just project management or troubleshooting, balancing your technical and project management skills
- Have a solid understanding of process control systems and automation
- Are skilled at planning and tracking project activities and schedules
- Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements
- Have demonstrated strengths with strong interpersonal, cross-cultural communication
- Are adept at building and maintaining relationships and leading without direct authority
- Show resiliency and flexibility in the face of challenging situations
Qualified candidates must have a minimum of a Bachelor's degree in engineering, preferably Chemical Engineering or Biochemical Engineering and the following minimum years of experience in project/process engineering or an equivalent combination of advanced education and experience.
- Senior Project Engineer: 5+ years
- Principal Project Manager - Engineering: 8+ years
Direct experience with biopharmaceutical process equipment is preferred. Level will be determined based on qualifications relevant to the role.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
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.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
$87,000.00 - $166,000.00
Top Skills
What We Do
At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.
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