Supervisor - Production - Night Shift

Our Frederick Manufacturing Center (FMC) creates life-changing medicines for people around the world and has been recognized by our local community as being a Top 50’ Business in Frederick and awarded Frederick County’s Best Place to Work’.

This distinctive biologic manufacturing facility, with over 800 employees, makes a direct contribution to treating people with cancer, respiratory and autoimmune conditions across the globe.

We work hard to deliver life-changing medicines to patients, and we take time to have fun and celebrate our accomplishments.

From catered site festivities to competitive events, community outreach activities, environmental and wellness showcases and team-building functions, we take time to recognize our achievements and celebrate our diversity.

We are dedicated to creating a culture of inclusion and collaboration and are committed to continuous learning by offering ongoing skill building and training for our staff.

Fueled by our aspiration to deliver accelerated growth for our company and to make people’s lives better, there’s never been a more exciting time to join the team and shape the future of AstraZeneca Operations.

Shift : 6pm-6 : 30am (2-2-3 schedule)

Join us as a Production Supervisor in our Operations department, where you will be responsible for daily supervising and performing on-the-floor operations pertaining to biologics manufacture in a cGMP environment.

This role is an exciting opportunity to adapt and innovate at pace, experiencing the thrill of launching new products and developing innovative processes.

Accountabilities :

As a Production Supervisor, you will be responsible for coaching, counselling, training / development, discipline and recognition of direct staff, including performing annual performance reviews.

You will ensure the performance of all process steps specific to the phase or stage of operation and execute production and resource schedule against operational plan.

Off-floor support will also be part of your responsibilities, including generating SOPs, MPRs, and SPRs for equipment and procedures used in routine biologics manufacture.

Essential Skills / Experience :

• 5-7 years work experience in pilot or commercial biologics manufacturing under cGMP with Bachelors.
• 3-5 years experience with Masters degree.
• 10-15 years experience with Associates Degree
• 15+ years experience with High School education.

Desirable Skills / Experience :

• BS / BA degree preferred in biological sciences or biotechnology / life sciences.
• Masters degree accepted.
• Associates and High School Diploma acceptable with appropriate experience

At AstraZeneca, we are driven by the challenge to stay ahead in rapidly changing markets as we continuously seek new and better ways to deliver medicines all the way to our patients.

Our resilience helps us to thrive as we innovate and evolve. We foster an encouraging, positive environment where ideas are welcomed and rewarded.

If you are self-driven, thrive at pace, continuously learning and proactively taking on more, then AstraZeneca is the place for you.

Ready to make a big impact? Apply now and join us in our mission to deliver life-changing medicines!

Date Posted

12-Jun-2024

Closing Date

Our 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.AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.