Join us as a Principal Process Engineer, where you'll be at the forefront of resolving technical issues, optimizing processes, and implementing new equipment. This role is a unique opportunity to break new ground and leave a collective legacy in our Operations department. You will report to the Director of Engineering.
You Will:
Design and implement new systems and equipment.
Develop and implement strategies for the maintenance and development of utilities and infrastructure.
Analyze current systems and processes to recommend improvements and innovations.
Provide expert advice on utilities systems including electricity, water, gas, and waste management.
Address and resolve any issues or concerns related to infrastructure and utility operations.
Implement best practices for risk management and environmental compliance.
Advocate for sustainable practices and innovative approaches to infrastructure challenges.
Provide input to the site master plan and capital portfolio.
Lead change control and management.
Evaluate new technology for GMP manufacturing equipment, Utilities, and Site Infrastructure.
Interact with the automation team.
Manage or support capital projects.
Lead or support validation activities and provide technical support during cGMP audits.
Train manufacturing and facilities staff on equipment operation and contribute to operational continuous improvement initiatives.
Provide leadership to less experienced engineers, technicians, and staff.
You Have:
Bachelor’s degree in engineering/life science.
Minimum of 10 years of Engineering Experience in a GMP environment.
Minimum of 10 years of Biopharmaceutical industry experience.
Experience in applying engineering best practices, methodologies, tools, software, and principles.
Experience leading a team of engineers or a cross-functional team.
Experience in systems such as SAP, Quality Systems, CAD, document management systems, and SharePoint.
Continuous improvement mindset: LEAN experience is strongly preferred.
Broad understanding of the technical/operational stages of production processes and project execution.
Excellent written and verbal communication skills.
Preferred Qualifications:
Experience in process automation.
Experience in managing complex projects within time and budget constraints.
Experience with regulatory inspections and internal audits.
The annual base salary for this position ranges from $129,859.20 to $184,288.80. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Our Benefits:
Benefits offered include:
A qualified retirement program [401(k) plan]
Paid vacation, holidays, and paid leaves
Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.
#celltherapy #LI-Onsite
Date Posted
20-Mar-2025Closing Date
29-May-2025Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.
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