Manufacturing Supervisor Jobs

Do you have expertise in, and passion for problem-solving, leading teams, and continuous improvement in a GMP or regulated production environment? If so, then this position might be a great fit!

The AstraZeneca Newark Supply Site was established in 1971 and currently employs approximately 260 people. Over the course of these years, Newark has undergone many product portfolio changes since it first began as Stuart Pharmaceuticals through today as the designated AZ North America Packaging Center of Excellence and a Flexible Formulation site for the global supply of complex products. The site provides a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities. It’s important to us that you bring your full self to work every day. To help maintain your best self, here’s a sneak peek into some of the things this site provides: on-site fitness center access, lunch & learns, sustainable office working environment, team, site and family activities, life-long learning, diversity & inclusion, tuition reimbursement, and a dining center.

The Supervisor/Manager is a leader for the Process Operation team (ie. Manufacturing) and will be filled at either the Process Facilitator (Manufacturing Supervisor) or the Sr. Process Facilitator (Manufacturing Manager) level depending on the experiences and skills of the successful candidate.

What you'll do:

• Coach and provide feedback for performance management of direct reports. This includes building a positive work environment and career development opportunities for direct reports.
• Manage the Process / Package Operation to produce a high-quality product in accordance with the PET operating strategy. As a responsible leader for the operation, this must be done while maintaining effective employee relations and compliance to cGMP, other regulatory and SOX requirements, as well as Safety, Health & Environment obligations and AstraZeneca standards.
• Lead PET activity for a designated GMP asset or area to produce quality products with efficient use of equipment and materials including coordination of support staff, scheduling, and improvement initiatives. This coordination may be across shifts and across other Process Facilitators within the PET. Ensure that all Safety, Health & Environment standards and Quality cGMP’s are followed during the production of products.
• Communicate effectively through conveying information both to/from the shop floor and listening to their feedback/concerns.
• Accountable for the training of PET personnel on equipment, processes, and SOPs, including authoring, reviewing, and approving Standard Operating Procedures and other documents to ensure integration of cGMPs and improve process efficiencies.
• Work collaboratively to continuously improve the operation through rigorous problem-solving using LEAN tools and deviation investigations to recommend/implement solutions to improve the process measured by key performance indicators.

Qualifications:

Essential:

• Bachelor of Science in Engineering, Pharmacy, related Science or business

Process Facilitator / Manufacturing Supervisor:

• Problem-solving skills
• Proven collaboration / teamwork capability
• Effective communication and leadership skills
• Minimum two (2) years’ experience working in a regulated production environment (preferred) or industrial setting
• Knowledge of FDA cGMP’s

Sr. Process Facilitator / Manufacturing Manager

• Meet all requirements of the Process Facilitator
• Minimum five (5) years of demonstrated experience in GMP or regulated production environment
• Minimum of four (4) years of previous supervisory experience.

Desirable:

• Experience working in a LEAN manufacturing environment
• Strong mechanical, electrical, troubleshooting, and problem-solving abilities
• Ability to direct and participate in cross-functional teams
• Project management skills
• Training or experience in formulation, filling, packaging, validation, technology transfer, change control.
• Knowledge or previous experience in handling technical programs/projects
• Proven understanding of TDMS, Microsoft applications, SAP, Trackwise

Why AstraZeneca

At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth, and development.

So, what’s next

Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you!

Find out more on Social Media:

• About Operations https://www.youtube.com/watch?v=gak5Ham8oUw
• LinkedIn https://www.linkedin.com/company/1603/
• Facebook https://www.facebook.com/astrazenecacareers/
• Instagram https://www.instagram.com/astrazeneca/?hl=en