128 Manufacturing jobs in Ireland

**Manufacturing Engineer**
**23 month fixed-term role**
**Springhill**
**Who we want:**
+ **Collaborative partners.** People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers.** People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Goal-oriented developers.** Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions.
**What you will do:**
+ Ensure quality of process and product as defined in appropriate OS and
+ Material specifications.
+ Ensure GMPs and system safety.
+ Participate in FMEA, Control Plan, SOP and PPAP generation associated
+ with product transfers and scale ups.
+ Support capital acquisition activity from specifying equipment, contract
+ negotiation, Installation and validation.
+ Provide training for manufacturing team members.
+ Interface with Materials Science, Design and Quality Assurance departments
+ to provide customer with a quality product in a timely manner.
+ Validation, Appraisal and support of coating suppliers, machining suppliers
+ and raw material suppliers e.g. Forgings, titanium etc.
+ Communicate and participate in system and process troubleshooting with
+ support team members and with external agents.
+ Lead and participate cross functional and cross divisional process
+ improvement initiatives.
+ Provide engineering support for new product and new process introduction,
+ ensuring that all activities are completed and documented in accordance with
+ Stryker New product Development Process.
+ Process validation for products and processes; VP, IQ, OQ, PQ and
+ associated documentation.
+ Conduct Gauge R&R studies for products and new processes.
+ Carry out structured problem solving.
+ Application and development of statistical tools for use in driving continuous
+ improvement projects.
+ Provision of out-of-hours support to the business as required by management
+ or as mandated by shutdowns and/or equipment failures.
+ All other duties as assigned
**What you will need:**
+ Level 8 Degree in Engineering, Science or related discipline or equivalent technical experience.
+ 0- 2 years' experience in an Engineering role, ideally production, R&D, biomedical
+ Business understanding of operations and their impacts essential.
+ High level of PC and analytical skills required.
+ Flexibility essential.
+ Strong communication skills with both internal and external stakeholders.
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a dynamic and results motivated team
+ environment.
+ Experience in an FDA regulated or regulated industry is beneficial.
+ Experience in a Six Sigma and Lean Manufacturing environment with proven improvement results is beneficial
+ Green or Black Belt 6 Sigma qualifications are beneficial
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

Manufacturing Engineer
**At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.**
**Job Overview**
The Manufacturing Engineer in a sustaining role focuses on maintaining and improving existing manufacturing processes to ensure consistent production of high-quality medical devices. This role is integral to troubleshooting issues, implementing process improvements, and supporting ongoing production activities while maintaining compliance with regulatory and quality standards.
This includes advanced manufacturing processes such as, laser processing - cutting/welding, ultrasonic processing, coating processes, metal chemical processes and heat treatment, moulding/extrusion and component assembly.
**Job Requirements**
**Process Support & Troubleshooting:**
+ Provide day-to-day technical support to resolve production challenges, minimize downtime, and ensure stable operations.
+ Analyse root causes of production issues and implement corrective actions to address defects or inefficiencies.
**Continuous Improvement:**
+ Identify and implement opportunities to improve yields, reduce waste, and enhance overall production efficiency.
+ Utilize Lean Manufacturing, Six Sigma, and other methodologies to drive process enhancements.
**Change Management:**
+ Lead or support engineering changes (ECOs) to existing products, processes, or equipment.
+ Validate and document changes to ensure they meet quality, compliance, and operational requirements.
**Equipment & Tooling Maintenance:**
+ Ensure the continued functionality of production equipment through preventative maintenance programs.
+ Support equipment upgrades or replacements to improve reliability and performance **.**
**Collaboration with Cross-functional Teams:**
+ Partner with Quality, Operations,NPDand Supply Chain teams to address process deviations, non-conformances, and supplier issues.
**Documentation & Reporting:**
+ Maintain accurate process documentation, including SOPs, work instructions, validation protocols, and technical reports.
+ Track and report key performance metrics, such as yields, downtime, and defect rates.
**Health & Safety**
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
**What your background should look like**
**Qualifications & Key Requirements**
+ Engineering level 8 degree, or equivalent qualification.
+ Preferably a minimum of 3 years' experience in a similar roles
+ Strong problem-solving and troubleshooting skills.
+ Ability to prioritize tasks and manage multiple ongoing projects.
+ Excellent communication and collaboration skills to work with cross-functional teams.
+ Catheter assembly experience a definite advantage including braided/coiled shaft assembly and reflow, tip bonding and handle assembly.
+ Must be able to plan, organize, and implement multiple concurrent tasks and projects.
+ Jigs & Fixtures design and maintenance experience would be an advantage.
+ Demonstrate a practical understanding of lean manufacturing principles and statistics.
+ Equipment and Process Validation experience with working knowledge of Minitab software.
+ SolidWorks /AutoCAD skills would be an advantage.
+ Knowledge of ISO & FDA compliance.
+ Demonstrate a dynamic, motivated & flexible approach to work with results oriented attitude
#jobsEMEANR
#LI-ONSITE
**Competencies**
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork
**ABOUT TE CONNECTIVITY**
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( TE CONNECTIVITY OFFERS:**
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority!
- Competitive Salary Package
- Performance-Based Bonus Plans
- Health and Wellness Incentives
- Employee Stock Purchase Program
- Community Outreach Programs / Charity Events
- Employee Resource Group
**IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD**
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity **never requests

Purpose of Role:
The Manufacturing Engineer (ME) will provide engineering and process support to ensure successful implementation of 2D barcoding in line with EU MDR requirements.
This role will focus on supporting technical strategy execution, process validation, and operational readiness across both internal manufacturing and supplier sites.
Key Responsibilities:
+ Support technical execution of 2D barcode implementation, including validation activities (VP, IQ, OQ, PQ).
+ Partner with Quality Engineers (QEs) and Supplier Quality Engineers (SQEs) to assess and confirm laser marking equipment compatibility and process qualification at both supplier and internal sites.
+ Assist in First Article Inspection (FAI) preparation, reviewing supplier provided verification data and ensuring compliance to marking requirements.
+ Update and maintain manufacturing documentation (DCP, PFMEA, SOPs) to reflect new barcoding processes.
+ Collaborate with operations teams to ensure inspection readiness (visual inspection, barcode verifier checks).
+ Troubleshoot and provide technical support during initial marking trials and confidence runs.
+ Support scrap management, label obsolescence, and carton switchovers as required for Go-Live phases.
+ Actively contribute to risk assessments, ensuring process robustness and alignment with MDR and GMP requirements.
Required Skills & Experience:
+ 2-4 years' experience in a regulated manufacturing environment (medical device preferred).
+ Exposure to process validation and FAI/PPAP activities in a regulated environment.
+ Familiarity with laser marking or UDI/2D barcoding processes desirable.
+ Strong problem solving and root cause analysis capability (Six Sigma / Lean tools beneficial).
+ Proven ability to work collaboratively with cross functional teams (QE, SQE, and Operations).
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Project Engineer - Stryker Model Farm Road**
**(12-month FTC - with potential to extend)**
**Why engineering at Stryker?**
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development.
Need another reason to apply? Check out these 8 reasons to join Stryker's engineering team: we are looking for:**
+ **Detail-oriented process improvers** . Critical thinkers who naturally see opportunities to develop and optimize work processes - finding ways to simplify, standardize and automate.
+ **Collaborative partners** . People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.
+ **Analytical problem solvers** . People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
+ **Dedicated achievers.** People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
+ **Strategic thinkers.** People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.
**What you will do:**
+ Work with Engineering leaders to deliver business objectives through the application of engineering principles focused on quality, service, and cost.
+ Display proficiency in the use of process improvement and problem-solving manufacturing issues using Six-Sigma tools.
+ Providing technical leadership on all product and process issues and line performance monitoring to include performance management.
+ Development and implementation of appropriate supporting documentation, SOPs, and process work instructions compliant with current Good Manufacturing Practices (GMP).
+ Leading technical improvements under the business's Continuous Improvement Program (CIP).
+ Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
+ Conduct Gage R&R studies for products and new processes.
**What you will need:**
+ Level 8 degree in Engineering.
+ 0 to 2 years' experience in a manufacturing environment.
+ Demonstrable analytical and problem-solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment.
+ Excellent presentation and written / verbal communication skills.
+ Confident and effective decision maker, with a proven leadership ability to negotiate and influence others.
+ Proven Project Management skills through the delivery of business-critical projects.
**About Stryker**
Stryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better.
The company offers innovative products and services in Medical and Surgical, Neurotechnology, Orthopedics, and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 100 million patients annually.
More information is available at stryker.com ( role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Who we are:**
Abbott has a presence in over 160 countries and has over 113,000 employees. Our new manufacturing facility in Kilkenny (R95 A02A) is Abbott's 7th manufacturing site in Ireland.
The facility is a centre for world-class engineering, quality, medical device manufacturing. We have been making a difference in the lives of Irish people since 1946.
**Abbott Ireland**
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Kilkenny and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**What is this position:**
As Manufacturing Technician you will provide technical support relating to equipment utilized in the manufacturing areas by repairing, maintaining, or modifying production equipment.
Monitoring machine output on the shift to and ensure all cells are running to cycle time, to meet specific targets.
**What You'll Be Doing:**
+ Install and equipment validation
+ Conducting scheduled maintenance, diagnosing, and troubleshooting faults
+ Perform skilled maintenance and repair such as mechanical, pneumatics, electrical systems
+ Lead on maintenance and/or process issues
+ Ability to interpret blueprints and schematics.
+ Certifies and train manufacturing associates in the production processes.
+ Identifies and implements corrective actions for manufacturing related issues.
**How does this role fit into the organisation:**
You will report to a process Engineering Manager on a team of approx. 20. Your team will include process engineers and manufacturing technicians.
**What we're looking for:**
+ Min level 6 qualification (Trade or Third level equivalent)
+ Electrical and mechanical skills are desired
+ Technical and fault-finding skills
**What's in it for you:**
+ Pension
+ Healthcare
+ Bonus
+ Life insurance
+ Disability insurance
+ Paid maternity leave
+ Parental leave
+ Adoptive leave
+ Flexible working
Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

In this Manufacturing Engineering role, you will provide Engineering technical knowledge to resolve production issues and implement changes in a Medical Device Manufacturing Facility to support the sites Continuous Improvement journey. This will include providing technical leadership on cleaning, sealing and packaging Medical devices and working with the team to meet cell efficiency and monthly targets, improve reliability, reduce scrap and validation of new machinery and equipment.
This role will really suit an innovative problem solver with a positive attitude who enjoys a fast paced working environment.
Key Areas of Responsibility
+ Ensure quality of process and product as defined in appropriate OS and Material specifications.
+ Ensure GMPs and system safety.
+ Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
+ Provide training for manufacturing team members.
+ Interface with Materials Science, Design and Quality Assurance departments to provide customer with a quality product in a timely manner.
+ Validation, Appraisal and support of machining suppliers and raw material suppliers e.g. packaging components.
+ Communicate and participate in system and process troubleshooting with support team members and with external agents.
+ Lead and participate cross functional and cross divisional process improvement initiatives.
+ Provide engineering support for new Product and new process introduction, ensuring that all activities are completed and documented in accordance with Stryker New product Development Process.
+ Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.
+ Conduct Gauge R&R studies for products and new processes.
+ Carry out structured problem solving.
+ Application and development of statistical tools for use in driving continuous improvement projects.
+ All other duties as assigned.
**Key Requirements**
+ Level 8 Degree in Engineering, Science or related discipline
+ Has 0- 2 years' experience in a manufacturing environment.
+ Business understanding of operations and manufacturing principles.
+ High level of PC Skills required.
+ Flexibility essential.
+ Strong communication skills with both internal and external stakeholders.
+ Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
+ The individual should enjoy working in a dynamic and results motivated team environment.
+ Knowledge of FDA requirements.
+ Knowledge of six sigma and Lean Manufacturing
+ Ability to effectively work cross-functionally with Advanced Operations, Quality, etc.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

05 - Operations Engineering Support 2
Req ID:
Remote Position: No
Hiring Manager: Caroline Scully
Band: 05
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
**General Overview**
**Functional Area:** ENG - Engineering
**Career Stream:** OPE - Operations Engineering
**Role:** Technical Support 2
**SAP Short Name:** TS2
**Job Title:** Operations Engineering Support 2
**Job Code:** TS2-ENG-OPS
**Job Level:** Band 05
**Direct/Indirect Indicator:** Direct
**Summary**
The Equipment Maintenance Technician is responsible for the set-up, installation, maintenance and support of automated equipment ensuring optimum performance and the achievement of operational goals. The Equipment Maintenance Technician works closely with teams to resolve manufacturing issues and constraints while implementing safe and robust solutions to improve overall efficiency through improvement projects around run rate increase, cycle time gains, yields and quality.
This position for the day 8 AM - 8 PM Days.
This position will report to the Team Leader.
**Detailed Description**
- Repairs and troubleshoots electro/mechanical equipment failures.
- Schedules and performs preventative maintenance procedures.
- Helps move, install, set-up and refurbish equipment.
- Maintains accurate and up-to-date maintenance documentation.
- Records significant downtime issues and resolutions in appropriate databases.
- Interacts with other departments as required to co-ordinate equipment repairs.
- Works proactively to ensure performance targets are met; Yield/quality (using SPC/SQC)/production outs/up-time /process stability.
- Communicates potential problems that may affect capacity and quality to the Business Unit Team Leader as well as across zones/work areas where necessary.
- Attends pass-downs as required and provides status updates.
- Provides detailed inputs into failed spare parts management process.
- Supports Process Engineers to ensure Continuous Improvements are ongoing.
- Trains and assists other Technicians and Operators.
**Knowledge/Skills/Competencies**
+ Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes.
+ Strong troubleshooting/Problem solving skills.
+ Demonstrates a high level of technical ability, with hands on approach to solving technical issues.
+ Excellent written and verbal communication skills.
+ Good interpersonal skills and ability to work as part of a team.
+ Commitment to achievement of manufacturing excellence.
+ High level of flexibility: shift changes / training courses / preventative maintenance and Project support.
+ Ability to work on own initiative, is self-driven.
+ Resourceful, hands-on, enjoys a challenge.
+ Works well under pressure.
**Typical Experience**
- 2 - 4 years+ experience as a Technician in a high volume automated environment.
- Minimum Cert./Diploma/Senior Trades in Electrical/Mechanical Engineering or equivalent.
- Working knowledge of PLCs, Motor drives, pneumatic and hydraulic components is an advantage.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

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 Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
There are many ways to be a difference maker. Find yours.
We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport, on an initial 12 months fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring.
PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern, covering days, nights, weekdays and weekends.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more.
Your Key Activities will include, but are not limited to:
+ Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
+ Perform activities associated with the compounding, filling and capping of an aseptic process.
+ Prepare components and equipment for processing into a Grade A environment.
+ Accurately completing documentation on time, accurately and legibly.
+ Keeping the Manufacturing area tidy and clean.
+ Review and update documentation as requested by the Production Manager
+ Participating in root cause analysis and problem-solving.
+ Completing compliant investigations and environmental excursions.
+ Adhering to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
+ Follow gowning procedures on entry to areas
+ Report any machine issues to the Production Manager and the maintenance department.
+ Set-up, clean and maintain equipment
+

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 Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
AbbVie helps people around the world live better days and better lives each year. And that takes all of us.
We are now recruiting for a Manufacturing Analyst to join our newly formed Central Cervices Team in AbbVie Westport, Co Mayo on an initial 12 months fixed term contract.
Established in 1977, AbbVie Westport is a Centre of Excellence for Aseptic for Commercial manufacturing of Biologics & Eyecare (pharmaceutical) products. In this role you will be actively involved and manage the batch related CAPA's as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigations are complete in a timely manner.
If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more:
Key activities:
+ Use and maintenance of data within key systems such as SAP, S4HANA, Global Trackwise, POMs, One Track, One Vault and Compliance wire.
+ Document retrieval from local files and archives, as required for submissions, customer requests and others.
+ Tracking and Analysis of EM trends within the Eyecare Business Unit
+ Management of training curriculum for all using eLMS
+ Participate in and lead non-conformance and exception investigations as necessary.
+ Complete manufacturing investigations for LIRs.
+ Open and lead change control records using One Track.
+ Work with QA Teams to align and promote awareness on data integrity and good documentation practices.
+ Provide assistance when required at Regulatory Inspections.
+ Trending and co-ordination of customer complaints investigations.
+ Work close with Depts on corrective actions arising from Environmental excursions.
+ Comply with AbbVie policies and procedures and regulatory agency regulations.
Qualifications
Education and preferred experience:
+ Bachelor's degree in science, or a related field is preferred and/or a minimum of 2 years' experience in a similar role.
+ Detailed knowledge of CGMP and aseptic practices, data integrity requirements and GDP is required for this role.
+ Strong organizational skills and attention to detail are essential for this role.
+ Good interpersonal relations/communications 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: