169 Senior Manufacturing jobs in Ireland

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.

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).
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: 122868
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
+ Transfer of waste material out of the cleanroom areas
+ Perform environmental monitoring
+ Participate in media runs
+ Adhere to and support all EHS & E standards, procedures, and policies.
Qualifications
Education and Experience:
+ Leaving cert or equivalent qualification required, 3rd level qualification in a Science/Engineering or related discipline is preferred
+ 1-2 years GMP experience, preferably Aseptic/Sterile Manufacturing in a cleanroom environment
+ Experience working with SAP within a similar industry is preferable.
+ Strong communication, documentation, and IT skills.
+ Ability to multitask and adapt in a fast-paced environment.
+ Outstanding organization, flexibility, and time management skills
+ High attention to detail and methodical in approach
+ Ability to build strong relationships and work within cross-functional teams.
+ Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
+ Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
+ Team player who can collaborate with others to achieve organizational targets and goals.
So, does this all sound like the right role for you?
Then apply now and join AbbVie today!
#Monster
Additional Information
Multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) - a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.
At AbbVie, your individual contributions count - help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined. Sounds like the perfect career opportunity for you? We look forward to receiving your application! All you need is a complete CV - we will discuss everything else with you in person.
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:

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:

**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 ( 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

Catalyx are seeking a Manufacturing Technician to join our team and work a 24/7 (4 cycle) shift on our customer site in Cork. As a Manufacturing Technician, you will require a working knowledge of manufacturing methods and procedures in our customer's pharmaceutical tableting production facility. Who We Are : Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Work on routine assignments following established SOPS, Master Batch Record and cGMPs Perform moderately complex tasks associated with aseptic processing, dispensing, compaction, granulation, milling and coating Reporting any issue that needs to be resolved on line performance to Operations Lead Perform more complex troubleshooting unassisted Work on more complex manufacturing processes and assignments Clean (manually, and clean in place) and assembles equipment for production Perform detailed SAP (computerised software) and MES transactions in resolving inventory discrepancies Clean manufacturing area, including walls, ceilings, and floors Complete and maintain documentation related to assigned work, including log books, batch records etc Act as a point of contact for a compliance audit Operate drum coater and compression equipment or roller compactors Dispenses ingredients for batches Perform MBR manufacturing batch report updates Perform manual handling of product - loads and unloads tablets Deliver on agreed KPIs and metrics Other duties as requested Requirements: Three years relevant industrial experience in a cGMP manufacturing environment A relevant level 6 qualification is an advantage A technical/ engineering qualification or background is an advantage Excellent written and spoken communication skills with established interpersonal skills Proficiency in MS applications Demonstrates strong safety orientation with strict adherence to established safety practices and standards Detail orientated A can-do attitude towards customer delivery and performance Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Company description: WuXi Biologics is a world-class biologics services provider (from discovery, through to commercialisation) with global clients in the biopharmaceutical and healthcare industries. Our mission is to accelerate and transform discovery, development and manufacturing in the fast growing field of biologics to benefit patients worldwide. The company has sites/offices in China, US, EU, Asia. The company currently employs over 5,000 employees worldwide, and are providing services to over 200+ clients globally, including 13 of the top 20 biopharmaceutical companies. Job description: Manufacturing Director This position is the lead role for the MFG 7 Batch-Fed Single Use facility in the Manufacturing Department of the WuXi Biologics Manufacturing Organisation. The role is an integral part of the Manufacturing Department, responsible initially for the establishment of the MFG 7 facility during construction and commissioning and latterly the long-term leadership to ensure all customer requirements are delivered on time and in full. The MFG 7 Lead is responsible for building the MFG 7 Upstream and Downstream Teams in addition to the Manufacturing Technology technical group. The role is a critical leadership role on site requiring close collaboration with all functions on site. Organization Description WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. Were one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. Our mission is to accelerate and transform discovery, development, and manufacturing in the rapidly growing field of biologics to benefit patients worldwide. We have sites/offices in China, the US, the EU, Asia, and Ireland. We currently employ over 10,000 people and provide services to more than 600 customers worldwide, including the top 20 biopharmaceutical companies. Department Description As Manufacturing Director you will be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives. In this role you will report into the Senior Manufacturing Director. Your Responsibilities Key member of Manufacturing leadership team for WuXi Biologics Ireland. The incumbent will play an important role in the strategy and business planning processes, ensuring cross functional collaboration and leadership execution. The role will require extensive liaison with counterparts and business leaders in WuXi Biologics corporate to include the highest level of professional representation of the local site Manufacturing organisation. Support the development of the overall Manufacturing strategy aligned with the facilitys strategic business plans and global Manufacturing strategy. Build the newly formed MFG 7 Organisation in Dundalk establishing clear team identity, roles, responsibilities, and hand-over with other functions. Supervisor to the MFG 7 Upstream Lead, MFG 7 Downstream Lead, MFG 7 Innoculation Lab and Cell Bank Lead and the MFG 7 Manufacturing Technology Lead. Provide oversight of the design, construction, and qualification of the MFG 7 facility in Dundalk. Serve as MFG 7 drug substance (inclusive of Upstream cell culture and Downstream purification) process subject matter expert, providing technical oversight to teams, and coaching to associate staff. Technical Point of Contact for customers in relation to MFG 7. Providing technical and commercial leadership of: Oversight of day-to-day Upstream and Downstream manufacturing activities ensuring production timelines are met. Collaboration with QC & QA groups to ensure GMP compliance, manage deviation investigation and CAPA implementation, and support client auditing and agency inspections. All MFG 7 product quality related investigations and corrective or preventative action. Equipment, Facility and Documentation Changes within the facility. Collaboration with MSAT, Process Development and Project Management groups on technical transfer and process validation. New Product Implementation, including scale-up, through technology/process transfer to clinical and commercial manufacturing. Providing technical input to manufacturing process validation plans, protocols, and reports. Supporting all RFP business requests with required facility fits and technical information. Ensuring continual improvement of all manufacturing documentation (SOPs MBRs, OJTs) to ensure they are current, accurate, and clear. Communicate operational status regularly to senior management, as required, at the appropriate level of detail. Collaborate closely to assist the Senior Manufacturing Director in coordinating the work between the MFG 7 group and other functional groups to meet the production objectives and timelines. Authoring and reviewing standard operating procedures and technical reports. Support multidisciplinary teams (manufacturing science and technology, quality, analytics, regulatory) for process improvement and troubleshooting with end-to-end product focus. Perform all duties in accordance with GMP requirements, SOPs and controlled documents recommendations relating to production management activities. Flexibility to take on additional tasks and responsibilities at the discretion of the Senior Manufacturing Director. Will act as a role model for the manufacturing function and also the wider organisation in adherence to the WuXi corporate core values and PROUD culture. Your Profile The ideal candidate for this position, will have the following: Education: BSc in a scientific or engineering discipline is required. Masters level qualifications is advantageous. Knowledge/Experience More than 15 years experience in a cGMP biological manufacturing environment with previous experience managing and/or leading functional and project teams. Experience across both Upstream and Downstream manufacturing activities. Greenfield or large site expansion experience is beneficial. Experience working with lean principals and implementing CI processes within a complex manufacturing operation. Must have a proven track record of extensive manufacturing knowledge and experience gained within the biopharmaceutical/pharmaceutical industry sector. Significant expertise in manufacturing processes and systems. Proven track record in delivering large scale manufacturing projects. Technical Competencies Ideally, experienced in establishing a Manufacturing facility and large-scale design and construction project in a greenfield context of similar size and scale. Technology transfer to commercial facility and trouble shooting skills are important for this position. Demonstrated success in scientific and technical proficiency, bioprocess implementation, cGMP operation, and teamwork are critical for this position. Personal Skills: Excellent written and oral presentation skill, detail-oriented organizational skill, clear understanding of process control strategy and data management are also required for this position. Good decision making with strong judgment through collaboration and consideration of others point-of-view. Strong leadership competencies with demonstrated management skills Excellent people influencing and project management skills Self-motivated, flexible and creative leader, able to prioritize, multi-task, and work in a fast-paced & demanding environment. Onerous requirements: Must be willing to travel as required internationally to fulfil the responsibilities of the position As we extend our global reach, we need colleagues interested in change, in challenge, and in building a new future together. Reach beyond yourself and discover your true potential! If you have the ability to thrive in a dynamic and fast-paced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our vision - Any drug can be made, and any disease can be treated - dont miss out on this opportunity to join us and reach beyond yourself and discover your true potential. Apply now! Would you like to know more before you apply? Please visit us at or contact us via WuXi Biologics is an equal opportunities employer. Skills: Leadership MFG Bioprocessing Science Analytical Benefits: Bonus Parking Pension Sports & Social Club VHI