Supervisor Production - Night Shift at AstraZeneca

Posted in Other 12 days ago.

Location: Frederick, Maryland





Job Description:

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.


Join us as a Supervisor Production - Night Shift, where you will be responsible for daily supervising and performing on-the-floor operations pertaining to biologics manufacture in a cGMP environment. This role provides direction to subordinates using established policies and precedents, ensuring that projects are completed on schedule following established procedures and schedules.



Accountabilities:

As a Supervisor Production, you will spend 70-80% of your time on the shop floor, coaching, counselling, training/development, discipline and recognition of direct staff. You will also be responsible for ensuring performance of all process steps specific to the phase or stage of operation. Off-floor support provided includes generating SOPs, MPRs, and SPRs for equipment and procedures used in routine biologics manufacture, monitoring and creating documents and/or spreadsheets to support business reporting requirements, and collaborating with Manufacturing Process Lead to resolve problems.



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.


At AstraZeneca, our work in Quality is important and valued. We are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes. We are a team of ambitious people, who want to go far and we're all here to achieve. We take Quality seriously and there's a clear ambition to shift the mindset around Quality. It's more than just following procedures and regulations; it's about adding value for our patients, which ultimately benefits the business.


Join us in Operations and accelerate our Lean journey! Take advantage of the huge opportunities to drive efficiencies in our processes and produce better-quality outputs. Now is the time to join and make a bigger impact, as we commit and accelerate our growth in Lean.


Ready to make a difference? Apply now!


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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