Material Management Supervisor (2nd Shift 4PM to 12AM Mon-Fri)

PowerToFly; New Jersey; On-site; USD 105,000 - 145,000; Full time

Benefits offered by this job

Benefits package

Job summary

AbbVie is seeking a Supervisor of Material Management to lead a 12-person team in a cGMP manufacturing setting. You will drive safety, quality, and productivity while coordinating cross-functional projects and training compliance across the site.

Responsibilities include optimizing inventory, SOP management, and supporting site strategy with operations leadership. Strong leadership and GMP knowledge are essential.

Qualifications

• Bachelor’s degree or equivalent; eight+ years in manufacturing/production
• Strong computer proficiency and scheduling experience
• Understanding of GMP standards and quality systems
• Clear oral and written communication, and basic arithmetic
• Proficiency with MS Office and SAP

Responsibilities

• Leads and develops a team of material technicians in manufacturing operations
• Analyzes staffing needs to support 24/7 production
• Supports quality deviations and safety investigations
• Coordinates training and maintains 100% training compliance in FDA environment
• Reviews production documentation for completeness and accuracy
• Develops, writes, reviews, and updates SOPs
• Maintains inventory accuracy and stock levels for production supplies
• Ensures cleaning and housekeeping of production areas
• Prioritizes activities to meet planning and business objectives
• Supports site strategy and process improvements for long-term goals
• Collaborates cross-functionally on OpEx, projects, training, talent development

Skills

GMP knowledge

Communication skills

Critical thinking

Attention to detail

Writing skills

Education

Bachelor’s degree or equivalent

Tools

SAP

MS Office

Excel

Word

Access

PowerPoint

Job description

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

The supervisor of material management is responsible for the direct performance of the material management team. The individual is responsible for safety, quality, productivity, product movement and support of cGMP manufacturing operations. This role leads a team of 12 employees working in a collaborative environment to drive continuous improvement, maintain quality compliance, and resolve problems affecting production performance. Other key areas of responsibility include:

• Leads and develops a team of material technicians supporting manufacturing operations activities.
• Analyzes material management staffing needs to support 24/7 production operation.
• Supports quality deviations and safety investigations.
• Coordinates training and maintains 100% training compliance in an FDA regulated environment.
• Reviews documentations for production processing for completeness and accuracy.
• Develops, writes, reviews and updates Standard operating procedures as required.
• Maintains inventory accuracy and appropriate stock levels for all production supplies and tissue to support functions.
• Ensures cleaning and housekeeping of production areas are in compliance.
• Prioritizes activities to achieve planning and business objectives while driving positive engagement throughout all levels of the business.
• Supports development of site strategy, process improvements to achieve long term business objectives.
• Work cross-functionally to support all business initiatives, such as, OpEx, special projects, production training, talent acquisition, talent development, goal setting and performance development.

Qualifications

• Requires a bachelor’s degree or equivalent; Eight plus years’ experience in all aspects of manufacturing/ production processes.
• Computer proficiency, scheduling experience required and good writing skills.
• Demonstrate a clear understanding of GMP standards and quality systems.
• Demonstrated oral and written communication, critical thinking, basic arithmetic, and proper business etiquette skills.
• Computer proficiency including MS office (Excel, Word, Access, and Power point).and SAP.

Preferred

• 3+ supervisory experience highly desired.
• Experience in managing multiple shifts highly desired
• Experience in materials management desired.
• Ability to work in a cleanroom environment desired.
• Ability to work occasionally offshift.

Additional Information

• 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 employer 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

What AbbVie Has to Offer

Our work can—and does—have a tangible, lasting impact on millions of people. But it’s not just the results that matter. How we achieve them matters, too. Leading with purpose, we work to build a more sustainable future for generations to come. We do that by putting our expertise, resources and talent to work to make a real difference for patients, communities and our world.