Manufacturing Supervisor ; 2nd Shift

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience, and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit our website.

A2 Shift 2:30PM–11:00PM, Monday–Friday.

The Manufacturing Supervisor I role involves basic knowledge and experience in its field and develops competence by performing structured work. The position receives guidance and direction from more senior peers and leads and facilitates safe operations in line with all safety, regulatory and operational requirements. It assures the delivery of high levels of customer service, ensures quality of product and services, complies with all regulatory requirements, achieves desired financial performance including cost reductions, and builds a culture of high performance for the team.

• Ensure safety is the number one priority, driving safety improvements and conducting safety checks routinely. Promote a culture of zero safety incidents in compliance with all EHS requirements.
• Deploy team members daily and delegate tasks to meet the production schedule. Ensure team members are trained to the required standards, conduct regular 1:1s, performance reviews, and survey action plans. Approve time and attendance on time each week to ensure correct pay. Communicate effectively with team and cascade important information.
• Coordinate activities within the shift to meet the production schedule and ensure a smooth shift handover with the next manager.
• Maintain compliance with applicable regulatory agencies. Manage compliance issues promptly and conduct material checks, line clearance checks and spot checks routinely.
• Manage complete cycle time and continuously seek improvements, including change‑over time.
• Develop direct reports by securing appropriate training and assigning progressively challenging tasks. Ensure all personnel have development actions or plans in place and arrange opportunities for growth. Adopt a growth mindset toward personal development.
• Participate in process improvement initiatives to support Operation Excellence (OpEx).
• Generate and manage non-hazardous and hazardous waste in accordance with internal operating procedures and in compliance with local and federal regulations.

• Bachelor's degree required. A degree in sciences or engineering is strongly preferred.
• Pharmaceutical industry experience strongly preferred.
• Two years of manufacturing or related experience required; supervisory experience preferred.
• Proficiency in Microsoft Office and other manufacturing systems such as SAP.
• Working knowledge of safety, quality systems and cGMPs required; familiarity with documentation in a highly regulated environment and good writing skills.
• Experience working in an aseptic production environment desirable if applicable.

Compensation and benefits information will be provided during the interview process. The company offers a comprehensive benefits package including paid time off (vacation, holidays, sick), medical, dental, vision insurance and a 401(k) plan to eligible employees. The position is eligible to participate in the company's short‑term incentive programs.

Abb Vie is an equal‑opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer / Veterans / Disabled.

US & Puerto Rico only – to learn more, visit  Applicants seeking a reasonable accommodation,  to learn more: