Overview

The Rotational engineer will be a part of a two-year entry-level program. The program is designed to provide recent graduates accelerated training through real world, hands-on experience associated with roles and projects needed to support the business while promoting personal and professional growth for participants. Throughout the two years, you will be paired with a program mentor who will provide guidance and oversight of your development in the program.  

Why Patients Need You:  

Our breakthroughs would not make it to the hands of patients without our team members. We rely on a team of dedicated and agile colleagues, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them. 

What You Will Achieve:  

You will develop and enhance your communication skills as you may be responsible for leading project teams, participating in meetings, and providing presentations to other Pfizer colleagues at all levels of the organization.  You will gain knowledge on various departments throughout Gene Therapy and contribute to department projects. There is also an opportunity for you to be engaged in colleague resource groups and become certified in Lean/Six Sigma so you can obtain your Yellow Belt in the program.  Through this two-year program, you will have the opportunity to explore available full-time roles and find your permanent position at Pfizer. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. 

How You Will Achieve It:  

You will rotate through two to four fast-paced, collaborative, and diverse assignments in different disciplines within Gene Therapy Stage 1. These rotations are targeted to provide career growth and experience.  You will report to a department manager in each assignment who will oversee your day-to-day responsibilities. You will have the opportunity to gain experience in multiple disciplines that may include clinical manufacturing operations, clinical technical operations, clinical program management, automation, quality, manufacturing systems, manufacturing science and technology.  

You will be expected to: Conduct all activities that are in accordance with company policies and Standard Operating Procedures, global regulatory guidelines, environmental guidelines, etc. Be an actively engaged colleague that exemplifies our company values and our Actively Caring safety culture. Contribute to completion of project milestones and organize own work to meet project task deadlines. Provide input to support continuous improvement efforts, investigation corrective actions etc. Track and follow-up on assigned commitments, investigations, change controls, change control and general compliance initiatives. All other duties as assigned.  

Qualifications  

• Bachelor's Degree or master's degree in Engineering (Chemical, Mechanical, Industrial, Biomedical Engineering) or Life Sciences (Chemistry, Biochemistry, Microbiology) 

• Strong academic performance preferred (minimum 3.0 GPA)  

• Passion for learning and pursuing a career in the biopharmaceutical industry   

• Preferred experience within thebiopharmaceutical industry 

• Ability to perform mathematical calculations and learn new processes  

• Proactive in engagement with key stakeholders  

• Excellent verbal and written communication skills  

• Ability to efficiently use current computer packages including Excel, PowerPoint, MS Project and Word 

PHYSICAL/MENTAL REQUIREMENTS

Capable of sitting and/or standing for extended periods of time during the work shift.  

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Off shift extended days required intermittently to cover 24/7 biological processes. 

Relocation assistance may be available based on business needs and/or eligibility.