QC Supervisor
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.
Join us as a QC Supervisor in our Operations department, where you'll be responsible for the analytical and microbiological quality control of pharmaceutical manufacturing for Mt Vernon products. This role is a unique opportunity to face exciting new challenges every day, with the support of a dedicated team, in our constantly changing manufacturing environment.
SHIFT: 2nd shift start time will be between 12 and 2pm
Accountabilities:
As a QC Supervisor, you will serve as the primary link between the first shift and off-shift QC teams and production. You will coordinate workflow within your QC team, direct priorities and testing schedules for staff, and verify and approve QC data while monitoring for trends and abnormalities. You will also lead and assign projects, develop and maintain effective relationships with internal and external customers, regulators, and other stakeholders.
Essential Skills/Experience:
- Bachelor degree
- At least 5 years laboratory experience
- Strong organizational skills
- Strong understanding of technical areas related to lab operations (including instrumentation, statistical methods, and quality assurance)
- Ability to analyse and solve complex problems in a cross-functional team environment
- Demonstrated ability to work with, manage and develop people in a complex, changing environment
Desirable Skills/Experience:
- Bachelor degree in a Science subject (Chemistry, or closely related subjects)
- 7 years QC chemistry laboratory experience
- Project management experience
- Higher level degree
At AstraZeneca, we are leading our Operations function at an exciting time of growth and evolution. We pioneer new approaches and processes across our sites, empowering our teams to foster a Lean mindset and sustainable practices. Every change we make is to deliver better outcomes for our patients. We are inspiring and credible leaders, ensuring everyone on our site has a platform and opportunity to speak up and share their ideas. We are the champions of Lean, ensuring our teams understand and embody the benefits it can bring. There's improved quality and safety, as well as speed. Our manufacturing sites are environments of constant and rapid change. It's a place to expect the unexpected.
Are you ready to face the unexpected every day? Apply now to join our team!
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.
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