Manufacturing Supervisor I (Biologics, 3rd shift)

AbbVie'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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Purpose

• To lead and facilitate safe operations in line with all safety, regulatory and operational requirements.
• Assure the delivery of high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team.
• The role of Supervisor I has basic knowledge and experience in its field and develops competence by performing structured work. Receives guidance and direction from more senior peers.

Responsibilities

• Safety :Create an environment where safety is the number one priority in every activity that you do, driving safety improvements and conducting safety gembas routinely.
• Be present on the floor promoting a culture of zero safety incidents in compliance with all EHS requirements.
• People: Responsible for daily effective deployment of team members and ensuring tasks are appropriately delegated to meet the production schedule.
• Ensuring that team members are trained to the required standards of their job.
• Driving engagement with your team by having regular 1:1s, conducting performance reviews and having survey actions plans in place.
• Ensuring time and attendance is approved on time each week so that employees are paid correctly.
• Communicating effectively with your team to ensure important communications are cascaded.
• Compliance / Operational:
• Responsible for the effective coordination of the activities within the shift to meet the production schedule. 
• Ensure compliance with applicable regulatory agencies.
• Execute a proactive compliance management process where material checks, line clearance checks and spot checks are conducted routinely.
• Effectively manage any compliance issue that arises during shift that could potentially impact on lot completion.
• Ensure a smooth shift handover with the next manager to ensure departmental activities are planned and executed safely.
• Performance
• Responsible for complete cycle time management and continuously seek to identify improvements.
• Responsible for change-over time management and continuously seek to identify improvements.
• Development
• Develop direct reports by securing appropriate training and assigning progressively challenging tasks.
• Be proactive in self-development by having a growth mindset towards personal development.
• Ensures all personnel has development actions/ plans in place and arranging opportunities for growth.
• OpEx: Participates in process improvement initiatives.

• Bachelor’s degree is required.  A bachelor’s degree in sciences or engineering is preferred. 
• Experience in regulated pharmaceutical industry is preferred. Supervisory experience is not required.
• Proficient in Microsoft Office and other manufacturing systems, such as SAP.
• Working knowledge of safety, quality systems, and cGMPs is required. Familiarity with documentation in a highly regulated environment; good writing skills.
• Experience working in an aseptic production environment desirable.

The selected candidate must be available to work on the 3rd shift. 

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​​

​​

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​​

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​​

• This job is eligible to participate in our short-term incentive programs. ​​

​​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​

AbbVie 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html