Supervisor, Line I (M-F) 630am to 300pm.

Purpose

The Line Supervisor I will work in a high performing and fast-paced pharmaceutical finishing operation to meet our production requirements while maintaining the utmost focus on safety and quality. He or she will support setup changeover packaging equipment troubleshooting on multiple or improvement focused packaging lines. He or she will be expected to contribute to and influence a team environment by leading and working with his or her peers daily on finishing lines. He or she will be responsible for creating a safety and quality-focused environment by optimizing line resources to drive performance to meet or exceed production targets.

Responsibilities

• Satisfy responsibilities for the Line Supervisor I role.
• Demonstrated ability to actively manage line clearances for lot and list changes and blowing of the finishing line/equipment on multiple value stream(s).
• Work as a direct team member or a Production Technician on assigned line as required to maximize performance.
• Back up and support to Operations Coordinator.
• Effectively trains Line Supervisor candidates as qualified Subject Matter Expert.
• Identify implement and drive process improvement on dedicated lines focused on reducing human error increasing OEE and enhance yield
• Communicate and drive improvement opportunities through cross functional teams. Works closely with the production schedule and understands line priorities while working with minimal/limited supervision.

Qualifications :

• High School Diploma or GED required.
• 2 years cGMP or related manufacturing experience.
• Demonstrated knowledge of cGMP requirements in a regulated industry.
• Must be goal oriented able to lead within a team environment self-motivated and work with a sense of urgency to meet business needs. Ability to effectively influence team without direct authority over line personnel.
• Must possess strong organizational skills and the ability to make quick decisions.
• Computer skills and ability to learn new programs and applications required.
• Understanding and experience with production systems such as Enterprise Resource Planning Manufacturing Execution Systems etc. preferred.
• Requires standing up to 8-12hrs per day and lifting up to 25 pounds.
• Work 40 to 48 hours per week and may work as many as 60 hours depending on manufacturing demands.

Additional Information :

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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time