7 Shift Manager jobs in Ireland
Manufacturing Shift Manager

Posted 4 days ago
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Job 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 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. 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 is an advantage.
+ 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 & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Production Shift Manager
Posted today
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Manufacturing Shift Manager - Biologics

Posted 4 days ago
Job Viewed
Job 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 Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
Do your best work at AbbVie-as part of a brilliant, curious team
We are currently sourcing an experienced Manufacturing Shift Manager to join our Biologics Manufacturing team in AbbVie Westport on a permanent basis. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements.
This is a shift based role, you will be required to work 12-hour shifts between days and nights on a monthly rotation.
As part of your new and exciting role you will assure the long-term effectiveness of the team: deliver 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
Does this interest to you? then read on.
Here's a snapshot of your key responsibilities for this role:
+ Act as key point of technical contact for aseptic fill finish activities.
+ Supervision and execution of compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
+ You will lead, coach & mentor your manufacturing team, across a 12-hour rotating shift, to maximize the effectiveness through clear and effective communication of task details and goals to their team members, to allow the biologics technicians to work effectively
+ As part of this diverse and inclusive team, you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
+ Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner
+ We believe in collaboration so in this role, you will liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing
+ Resolve operations/project issues by working with team members, project customers, and others as appropriate.
+ Responsible for driving operations excellences and Key operations targets including OEE where applicable
+ Provides direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits
Qualifications
So, what do you need to do this role?
+ Minimum of 3 year's experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.
+ A minimum of 1 year team direct supervisory experience in a team environment
+ 3rd level qualification in a Science, Engineering or related scientific field, advanced degree is preferred
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
+ Has a technical background in pharmaceutical, biologics, or similar industries
+ Flexibility with working 12-hour shift, rotating between days and nights on a monthly rotation
+ Possess a strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions
So, are you ready now lead this ambitious and diverse Manufacturing team? Apply today!
It's important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment.
Additional Information
All your information will be kept confidential according to EEO guidelines.
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:
Trainee Production Shift Manager
Posted 9 days ago
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Clinical Nurse Manager(Night shift)
Posted 74 days ago
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Clinical Nurse Manager 2 (Shift leader) - PICU
Posted 4 days ago
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Clinical Nurse Manager 2 - Shift Leader - Emergency Department
Posted 5 days ago
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