Supervisor, Manufacturing I

Purpose

The role of the Manufacturing 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. 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.

Responsibilities

Must be able to work flexible hours (2 days on 2 days off 3 days on 3 days off) and every other weekend.

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 ensure tasks are appropriately delegated to meet the production schedule. Ensure that team members are trained to the required standards of their job. Drives engagement with team by having regular 1 : 1s conducts performance reviews and has survey actions plans in place. Ensure time and attendance is approved on time each week so that employees are paid correctly. Communicating effectively with team cascading important info.

Operational : Responsible for the effective coordination of the activities within the shift to meet the production schedule. Ensure a smooth shift handover with the next manager to ensure departmental activities are planned and executed safely.

Compliance : 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.

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. Ensures all personnel has development actions / plans in place and arranging opportunities for growth. Be proactive in self-development by having a growth mindset towards personal development.

Operation Excellence (OpEx) : Participates in process improvement initiatives.

Qualifications : Qualifications

High Diploma or GED required. Bachelors degree preferred. A degree in sciences or engineering is strongly preferred. Pharmaceutical Industry experience is strongly preferred.

Two years of manufacturing or related experience required. Supervisor experience preferred.

Must be able to work flexible hours (2 days on 2 days off 3 days on 3 days off) and every other weekend.

Experience Systems : Proficient in Microsoft Office and other manufacturing systems such as SAP.

Experience Regulatory : Working knowledge of safety quality systems and cGMPs is required. Familiarity with documentation in a highly regulated environment; good writing skills.

Experience Aseptic (If applicable) : Experience working in an aseptic production environment desirable.

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 ofthis posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic locationand 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.

This job is eligible to participate in our long-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 anybonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys soleand 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

Key Skills

Lean Manufacturing,Six Sigma,Continuous Improvement,FDA Regulations,Lean,Packaging,Production Planning,cGMP,Cell Culture,Leadership Experience,Supervising Experience,Manufacturing

Experience : years

Vacancy : 1