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Manufacturing Shift Manager

AbbVie

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AbbVie

Manufacturing Shift Manager

Onsite Kansas City, MO, United States Full Time Senior
Posted a day ago
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powertofly approved 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.

Job Details


Company Description

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.


Job Description

More than a job - It's a chance to make a real difference

Working at AbbVie is more than a job. It’s a career with meaning. A chance to make a difference, in the world and in your life. We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thrive—at AbbVie and beyond

 

We are now recruiting Shift Manager to join our diverse Unit Dose Eyecare Manufacturing team in Westport on an initial 12 month Fixed Term Contract.

Flexibility around shifts is essential for these roles as it will include a rotational shift pattern of Days and Nights.

Is this a team you want to be part of? Then read on… 

 

Purpose:

Lead and facilitate the safe operations of the primary container labelling process in the Unit Dose Department in line with all safety, regulatory and operational requirements. Assuring the long-term effectiveness of the team: delivering high levels of customer service, ensuring quality of product and services, complying with all regulatory requirements, achieving desired financial performance including cost reductions, and building a culture of high performance for the team

 

Responsibilities:

  • Act as key point of technical contact for coding and printing activities
  • On the floor Management and execution of equipment, preparation and support processing activities in the Eye Care facility to meet clearly stated operating objectives.
  • Team leadership, motivation and direction to maximize the effectiveness of your team, clearly communicating task details and goals to your team members, to allow them to work effectively.
  • Daily reporting on the status of all operations and support activities. Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
  • Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and clinical manufacturing/filling
  • Resolve operations/project issues by working with team members, project customers, and others as appropriate.
  • Drive operations excellences and Key operations targets including OEE where applicable.
  • Provides direct interface as a subject matter expert with QA department to interact with HPRA, FDA, applicable health authority and internal audits.
  • Develop direct reports by securing appropriate training, assigning progressively · challenging tasks and managing mid-year and annual reviews

 


Qualifications

  • You will have a Bachelor’s degree or equivalent required in an engineering or Science related field 
  • Minimum of 5 years’ experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry 
  • A working knowledge of safety, quality systems, and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required. familiarity with equipment and facilities validation
  • Must be flexible to handle multiple tasks including ability to handle pressure in a professional manner. Effectively work in a team environment. Maintain high level of energy and professionalism on the job. Build effective working relationships with customers, co-workers, cross-functioned groups, and management.
  • A minimum of 1 year direct supervisory experience in a team environment 
  • Intermediate to High computer and MS Office skills

Additional Information

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

Required Skills
  • engineering
  • science
  • batch processing
  • automation
  • commissioning
  • validation
Company Details
AbbVie
 Chicago, IL, United States
Work at AbbVie

Together, we break through We believe the paths we take to achieving our breakthroughs matter. At AbbVie, every one of our 50,000 employees is a... Read more

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