Process Coordinator - Military Veterans

The Philadelphia, PA site manufactures a life-saving influenza vaccine. Our product is aseptically filled into sprayers for nasal administration. The site consists of two geographic locations - a production facility at Red Lion Road in NE Philadelphia and a storage and distribution facility in Bensalem. The two facilities employ approximately 140 employees. The facilities are about 8 miles apart and both are situated close to I-95, the city of Philadelphia, and Philadelphia International Airport. Our product is sold in the US, UK, and other countries. Operations continue year-round, with the production season being in the summer (typically May-August). Our site is highly collaborative where we show our Philly pride in all we do. We work closely together, always striving to be better every day. We have a network of employee teams who deliver many kinds of employee engagement activities, from our famous Wingbowl, to inclusion events, site celebrations, community outreach, health and wellness activities

This is 2nd shift working M-F 2pm - 10:30pm.

Accountabilities:

As a Process Coordinator, you'll ensure schedule adherence and recommend alternatives to scheduling exceptions. You'll be responsible for SAP transactions, perform SOP revisions, and coordinate trainers for on-the-job training. You'll also liaise with QA, Facilities, and QC to ensure timely batch release. Other tasks include reviewing completed batch records, receiving requests for future activities which may impact the production schedule, monitoring schedule via computer terminals and adjusting as needed. You'll provide communication to affected departments of schedule changes in a timely fashion and communicate to adjacent shifts, changes and events which may affect production schedules.

Essential Skills/Experience:

- High School Diploma or general education degree (GED)

- 1 year of experience in pharma/biomed industry

Desirable Skills/Experience:

- Bachelor's degree is preferred

- 2 years related experience; experience with GMP in a pharmaceutical environment preferred.

When we put unexpected teams in the same room, we unbind bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we workthe entire shift onsite, but that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and bold world.

Why AstraZeneca?

At AstraZeneca, we are at an exhilarating time of new products and launches. We work with innovative and scientific products on our pioneering end-to-end supply chain, using the latest technologies and modern facilities. We are active players in growth and evolution, promoting a Lean approach and leading on sustainability. As a global business in stable growth, there are long-term opportunities and multiple pathways to take. We foster an encouraging, positive environment where ideas are welcomed and rewarded. If you want to make a big impact, this is the place for you. Our contribution to life-changing medicines is why people have been here for decades. We do it for the patients.

Ready to embrace constant challenges and work at the cutting-edge? Join us! Together we can push the boundaries of Supply Chain and shape our future with a big contribution to life-changing medicines.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.