What are the responsibilities and job description for the PET Formulation - Process Engineer position at AstraZeneca?
Job Description
The AstraZeneca Mt. Vernon site was established in 1972 and is the flagship site delivering innovative, life changing oral solid medicines. At the site we formulate and pack OSD tablets and capsules for over 60 markets. The Mt Vernon site is complex, the largest AZ production site in the US with over 700 employees. We are located in the southwest corner of the state of Indiana, approximately 15 miles from Evansville, Indiana – the third largest city in the state. The Mt. Vernon site is both collaborative and Inclusive. We have several employee resource groups (ERGs) onsite that are aimed at promoting, celebrating, and educating employees about diversity, inclusion, philanthropy, networking, etc. Each of these groups provide employees with opportunities for interactive and engaging events and initiatives which enhance professional development and provide opportunities to engage with likeminded co-workers.
It is important to us that each employee feels welcome to bring their whole self to work every day. Here is a sneak peek of some of “perks” the MTV site offers: on-site fitness center with access to a personal trainer, on-site walking trail, walking desk, on-site basketball court, ping pong, massage chair, lunch & learns, sustainable & ergonomic office working environment, tuition reimbursement, training/ lifelong learning opportunities, book club, dining center with hot meals, snack market, free coffee and hot tea, climate controlled work environment.
Are you ready to break new ground and leave a collective legacy? As a PET Formulation - Process Engineer, you will provide technical support for process manufacturing, investigating and correcting process-related problems and deviations from standards. This role offers the opportunity to play a pivotal part in evolving our Supply Chain, reimagining how we do things, and creating a lasting impact.
Accountabilities
Ready to take ownership and reshape the ecosystem? Apply now!
The AstraZeneca Mt. Vernon site was established in 1972 and is the flagship site delivering innovative, life changing oral solid medicines. At the site we formulate and pack OSD tablets and capsules for over 60 markets. The Mt Vernon site is complex, the largest AZ production site in the US with over 700 employees. We are located in the southwest corner of the state of Indiana, approximately 15 miles from Evansville, Indiana – the third largest city in the state. The Mt. Vernon site is both collaborative and Inclusive. We have several employee resource groups (ERGs) onsite that are aimed at promoting, celebrating, and educating employees about diversity, inclusion, philanthropy, networking, etc. Each of these groups provide employees with opportunities for interactive and engaging events and initiatives which enhance professional development and provide opportunities to engage with likeminded co-workers.
It is important to us that each employee feels welcome to bring their whole self to work every day. Here is a sneak peek of some of “perks” the MTV site offers: on-site fitness center with access to a personal trainer, on-site walking trail, walking desk, on-site basketball court, ping pong, massage chair, lunch & learns, sustainable & ergonomic office working environment, tuition reimbursement, training/ lifelong learning opportunities, book club, dining center with hot meals, snack market, free coffee and hot tea, climate controlled work environment.
Are you ready to break new ground and leave a collective legacy? As a PET Formulation - Process Engineer, you will provide technical support for process manufacturing, investigating and correcting process-related problems and deviations from standards. This role offers the opportunity to play a pivotal part in evolving our Supply Chain, reimagining how we do things, and creating a lasting impact.
Accountabilities
- Provides technical support for Formulation areas, including investigation and correction of process-related problems and deviations from standards.
- Responsible for identifying and executing projects to reduce product cost, improve product quality, improve yield, and reduce material usage.
- Collaborates with Production, Engineering, Automation, and Quality to optimize productivity, yield, product quality, and supply reliability.
- Designs and executes process and cleaning qualifications and validations.
- Initiates Formulation area change proposals as required for projects managed by the Process Engineering group.
- Updates, reviews, and approves area procedures to ensure correct content and compliance with Good Manufacturing Practices.
- Authors, reviews, and approves Formulation master batch records.
- Assists as a subject matter expert for technical projects affecting Formulation during internal audits and regulatory inspections.
- Supports technical transfer and implementation of new technologies, equipment, and processes from R&D and other sites to the Mount Vernon site.
- Bachelor’s degree required, preferably in Science, Chemical Engineering, or other related technical discipline.
- 0-1 year of Industry Experience
- Strong understanding of cGMPs, demonstrated leadership, management, and technical capabilities.
- Excellent verbal, written, and interpersonal communication skills are essential.
- Must have demonstrated ability to plan, implement, and achieve significant, complex goals and objectives.
- Demonstrated ability to organize and implement projects that improve the operational effectiveness of process manufacturing.
- Master’s degree or 2 years’ relevant experience is highly desirable.
- Experience with IQ/OQ/PQ and Lean Manufacturing is highly desirable. Six Sigma certification is preferred.
Ready to take ownership and reshape the ecosystem? Apply now!
