7 Cell Lead jobs in Ireland

Lean Manufacturing & Production Supervisor ? County Cavan ? Packaging Manufacturer Overview Are you a hands-on leader with a passion for lean manufacturing and continuous improvement? A well-established packaging manufacturer in County Cavan is seeking a Lean Manufacturing & Production Supervisor to join their team. This is a pivotal role that blends day-to-day production oversight with strategic lean initiatives, offering the opportunity to make a real impact on operational performance and team development. Responsibilities Lead daily production operations to meet output, quality, and safety targets. Champion Lean Manufacturing principles across the plant. Drive continuous improvement through Kaizen, 5S, and Value Stream Mapping. Monitor and report on KPIs including efficiency, downtime, and quality. Collaborate with maintenance, quality, and logistics teams. Mentor and train staff in lean tools and best practices. Support SOP development and contribute to capital projects and upgrades. Criteria Proven experience in a supervisory or team lead role within manufacturing. Strong working knowledge of Lean Manufacturing tools and techniques. Excellent leadership, communication, and problem-solving skills. Ability to inspire and develop high-performing teams. Experience in production planning and performance tracking. A technical or engineering qualification is a plus, but not essential. Reward Competitive salary and benefits package. A key role in shaping the future of production operations. Ongoing professional development in lean and leadership. A collaborative, innovative, and forward-thinking work culture. Ready to Lead Change? If you're driven by efficiency, passionate about people, and ready to take the next step in your manufacturing career, we want to hear from you. Apply now to be part of a company that values innovation, teamwork, and continuous improvement. At Wallace Myers International Recruitment Agency we specialise in sourcing professionals for key industries and services. See our website for more details. Privacy Policy: By applying for this role you are agreeing that your details will be stored in our database and may be considered for similar future positions. For more info see Skills: Production Supervisor Manufacturing Engineer Lean Manufacturing

Company description: . Job description: Work Your Magic with us! Ready to explore, break barriers, and discover more? We know youve got big plans so do we! Our colleagues across the globe love innovating with science and technology to enrich peoples lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us. The Role The Manufacturing Maintenance Supervisor is responsible for directing and coordinating all technical and maintenance activities in support of production in a safe, cost-effective and environmentally friendly manner, assuring capacity and achieving plant performance metrics. Duties Include: Lead Technical Team with a key focus on timely completion of PMs, Calibrations (on or before due date on SAP) and Equipment Downtime Resolution. Responsible for the development and tracking of the departments KPIs in order to measure equipment and maintenance performance i.e. MTBF, MTTR, OEEs, schedule attainment, labour utilisation, work order backlog, PM / calibration completion rates, spare usage and costs control. Responsible for all maintenance information including specifications, drawings, manuals and SOPs are up to date and located in shared folders for access and retrieval by colleagues. Follow the appropriate SAP Next procedures. Use defined maintenance data generated allied to equipment and business understanding of site needs and impact (e.g. knock-on effects of poor equipment reliability) to justify capital expenditure. Plan, organise, direct and control maintenance project activities to meet defined site objectives and to provide technical support to the maintenance group by taking the lead on issues. Develop scientific risk-based approach to identifying key critical spares for plant and equipment and ensure that critical spares are in stock or are always readily available. Ensure that an effective program is then maintained. Placement of Purchase Orders for equipment and spares is within the job role as is other administration work required to carry out your functional work. Setup of SLAs as appropriate. Timely resolution of Unplanned Works and recording of resolution, resource hours, costs via SAP Work Order. Work with the Planner (where applicable) to setup Optimised PM and Calibration Frequencies. Present technical data and lead tours of internal and external audit groups and customer visits Manage on site contractors under area of responsibility including the preparation of all required work permits and the review of risk assessments and method statement for the required tasks or work. Ensure that comprehensive maintenance documentation exists for each equipment item & that it is filed in an organised & legible manner in the designated shared folders. Ensure strict compliance of GMP and SOP procedures during the diagnosis, repair and maintenance of mechanical, electrical, instrumentation and electronic plant and systems associated with producing the finished products. Lead shutdown activities including planning, execution and lessons learnt. Travel as appropriate to support project FATs, development work or training as needed. Reporting of equipment and process performance utilising OEE tools to identify and address efficiently losses i.e. Availability x Performance x Quality. Formal Setup of Equipment associated Spares, PMs and Calibrations in SAP. Manage the department discretionary spend and capital budgets on a monthly and quarterly basis and avoid overspends. Lead and drive continuous improvement initiatives identified through on-going assessment of equipment issues and reliability (based on gathered data and statistical analysis). Who You Are Minimum 8+ years experience in an Engineering / Maintenance Leadership role, preferably within the Life Science, Medical Device and / or Pharmaceutical Industry. Engineering Degree (Minimum Level 7, Level 8 an advantage) in Mechanical or Electrical Engineering or recognised equivalent. Experience or Qualification in Reliability Engineering an advantage. Trades Qualified an advantage. Work Experience High level of energy, positivity and enthusiasm and the ability to motivate others. Demonstrated high performance history, proven ability to execute and get results. Excellent leadership, facilitation, and communication skills Strong project management experience Ability to influence within a matrix organisation with direct and indirect authority. Ability to work with employees at all levels of the organisation. Experience with planning and executing change within a high work paced environment. Keen ability to teach and coach. Preferable experience with SAP Next / PM system. Preferable experience with a Calibration System. Previous experience within an ATEX environment an advantage. Experience with Planned Preventative and Proactive Maintenance approaches. Excellent awareness and experience in relation to Quality and Environmental Health and Safety Skills The ability to work effectively within a team environment. Lead a high performing technical group. Keen to learn & take responsibility. Analytical with experience in Lean Six Sigma Methodologies Familiar with GMP requirements within a regulated industry. Effective verbal, written & interpersonal communication skills. Self-motivated. Strong organisational, time management and planning ability. Computer Literate Excel, Word, Powerpoint etc. Methodical Work Approach. Profile description: Please see Job Description We offer: What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life! Skills: Maintenance Engineering People Management Benefits: Bonus Health Plan Pension

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. For more information, visit  embecta.com  or follow our social channels on  LinkedIn ,  Facebook ,  Instagram  and X ( . 
**Why join us?**
A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work.  Here our employees can fulfill their life's purpose through the work that they do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture.  Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees.
**SPN Production Team Leader**
+ Reporting to the SPN Value Stream Leader, the SPN Production Team Lead role is responsible for coordinating production activities across Safety Pen Needle operations in addition to being a critical partner with relevant stakeholders including PQS Operators, Technicians, Process Engineering and QA Personnel
**Responsibilities**
+ Coordinate and lead the shift SPN team to meet SQDCP goals.
+ Champion safety within the cell and promote a positive safety culture within the team.
+ Work as part of a team to ensure optimum flow of units through the production process.
+ Ensure compliance with Work Instructions, SOP's and GMP requirements at all times.
+ Identify opportunities to improve work processes and methods as part of site CI/ Op Ex program.
+ Assist in drawing up and communicating production schedule plans - liaise with buyer / planners and moulding suppliers as required.
+ Monitor hour-by-hour performance across the assembly cell and support the team to improve performance where required and escalating where appropriate.
+ Champion the NOE Quality process within the cell and ensure the team are raising NOEs for defective / suspected defective materials and support the material investigation to conclusion.
+ Review documents in the device history records to ensure accuracy and timely completion.
+ Work in conjunction with the Shift Manager and Training Team to develop team cross skilling capabilities.
+ Liaise with the Quality department as required . Manage any sampling of lots and document as appropriate.
+ Manage levels of WIP and take appropriate decisions with relevant personnel to
+ Monitor raw material inventory and take action to address where required.
+ Support the shift teams in managing work order accuracy to 100%
+ Ensure production area is compliant with required quality standards
+ As required, be involved in project planning and future developments.
+ Perform other duties as assigned by management
**Educational Requirements and Relevant Experience:**
+ Second-level qualification coupled with appropriate experience
+ Training in Good Manufacturing Practices
+ Relevant Further Education - eg: Supervisory/Production management or Quality
**Relevant Experience:**
+ Minimum of 3 years' experience in a regulated manufacturing environment
+ Leadership/Coordination experience in a production operation
+ Lean Manufacturing
+ Excellent documentation skills and attention to detail
+ The ability to follow tasks through to completion
+ Knowledge of Standard Operating Procedures.
+ Excellent interpersonal and communication skills
+ The ability to work as part of a team and on your own initiative
+ Good PC skills
+ Proactive - someone who anticipates potential problems and is a step ahead.
embecta is an Equal Opportunity/Affirmative Action Employer.  We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

embecta is a global diabetes care company that is leveraging its 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of more than 2,000 employees around the globe. Why join us? A career at embecta means being part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here our employees can fulfill their life's purpose through the work that they do every day. You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program - which includes competitive pay, benefits, continuous learning, recognition, career growth and life balance components - is designed to support the varying needs of our diverse and global employees. SPN Production Team Leader Reporting to the SPN Value Stream Leader, the SPN Production Team Lead role is responsible for coordinating production activities across Safety Pen Needle operations in addition to being a critical partner with relevant stakeholders including PQS Operators, Technicians, Process Engineering and QA Personnel Responsibilities Coordinate and lead the shift SPN team to meet SQDCP goals. Champion safety within the cell and promote a positive safety culture within the team. Work as part of a team to ensure optimum flow of units through the production process. Ensure compliance with Work Instructions, SOP's and GMP requirements at all times. Identify opportunities to improve work processes and methods as part of site CI/ Op Ex program. Assist in drawing up and communicating production schedule plans - liaise with buyer / planners and moulding suppliers as required. Monitor hour-by-hour performance across the assembly cell and support the team to improve performance where required and escalating where appropriate. Champion the NOE Quality process within the cell and ensure the team are raising NOEs for defective / suspected defective materials and support the material investigation to conclusion. Review documents in the device history records to ensure accuracy and timely completion. Work in conjunction with the Shift Manager and Training Team to develop team cross skilling capabilities. Liaise with the Quality department as required . Manage any sampling of lots and document as appropriate. Manage levels of WIP and take appropriate decisions with relevant personnel to Monitor raw material inventory and take action to address where required. Support the shift teams in managing work order accuracy to 100% Ensure production area is compliant with required quality standards As required, be involved in project planning and future developments. Perform other duties as assigned by management Educational Requirements and Relevant Experience: Second-level qualification coupled with appropriate experience Training in Good Manufacturing Practices Relevant Further Education - eg: Supervisory/Production management or Quality Relevant Experience: Minimum of 3 years' experience in a regulated manufacturing environment Leadership/Coordination experience in a production operation Lean Manufacturing Excellent documentation skills and attention to detail The ability to follow tasks through to completion Knowledge of Standard Operating Procedures. Excellent interpersonal and communication skills The ability to work as part of a team and on your own initiative Good PC skills Proactive - someone who anticipates potential problems and is a step ahead. embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

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
We are seeking a highly motivated and experienced Operations Shift Supervisor to join our Drug Product Pharmaceutical manufacturing team. In this key leadership role, you will oversee the safe and compliant production of drug product materials, ensuring all operations meet regulatory, safety, and organizational standards.
You will lead a team of pharmaceutical technicians, drive continuous improvement, and play a crucial part in maintaining AbbVie's reputation for quality and excellence.
Key Responsibilities:
+ Supervise and execute pharmaceutical processing activities to meet operational objectives.
+ Lead, motivate, and develop a team of 10-12 direct reports, ensuring clear communication of tasks and goals.
+ Plan resources and coordinate training to ensure safe and efficient operations.
+ Measure, report, and own key departmental performance metrics (yield, rate, usage, attendance, overtime, etc.).
+ Ensure compliance with all safety, environmental, and quality SOPs.
+ Collaborate with other shift supervisors and internal/external stakeholders to ensure smooth interdepartmental operations.
+ Manage employee relations, performance reviews, and growth plans in partnership with HR.
+ Maintain accurate personnel records and update manufacturing control systems.
+ Support and implement key site and departmental strategies.
+ Adhere to all EHS & E (Environment, Health, Safety & Environment) standards and policies.
+ Lead and participate in continuous improvement initiatives.
+ Represent your area during regulatory inspections and audits.
Supervision & Leadership:
+ Operate with a high degree of autonomy, reporting to the DP Operations Leader.
+ Set annual goals, conduct performance reviews, and manage team development.
+ Act as a site Subject Matter Expert (SME) for DP Manufacturing issues.
+ Provide technical leadership and collaborate with key stakeholders.
Qualifications
+ Diploma in a relevant science or engineering discipline, or equivalent experience.
+ Minimum 3 years' experience in batch processing operations within an FDA/HPRA regulated pharmaceutical environment.
+ Detailed knowledge of cGMP and regulatory requirements.
+ At least 3 years' experience in a highly automated environment.
+ Minimum 3 years' direct supervisory experience or relevant training.
+ Proven experience leading teams and participating in improvement programs.
Skills & Attributes:
+ High attention to detail and commitment to compliance.
+ Innovative thinker with strong problem-solving skills.
+ Results-driven, with the ability to prioritize and meet business demands.
+ Strong verbal and written communication skills.
+ Excellent interpersonal and leadership abilities.
+ Demonstrates integrity, a strong work ethic, and a "Right First Time" mindset.
+ Flexible to meet business needs, including shift work.
Additional Information
Why AbbVie? Join a global leader in the pharmaceutical industry, where you'll have the opportunity to make a real impact, develop your career, and work with a passionate team dedicated to improving lives.
How to Apply: If you are ready to take the next step in your career and lead a high-performing team in a world-class manufacturing environment, we want to hear from you!
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.
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Lead Production Operator Our client is a world leader in diagnostics for clinical healthcare, toxicology and food security and they are looking to add a Lead Production Operator to join their Manufacturing department in Dungloe, County Donegal. What does the Biochip team do? The Biochip team manufacture products for use across the Biochip Array Technology Analysers. Our clients cutting-edge technology is used in Laboratories and Hospitals to diagnose health tests as wells as veterinary samples, and food testing. Location: Dungloe, County Donegal. Contract Offered: Full-time, permanent. Working Hours / Shifts: 4 days week. 7am-5:40pm. Monday to Thursday. What does the Lead Production Operator role involve? The role of Lead Production Operator will be working on the production of the Biochip Array products. A varied role with preparation of buffers, operation of automated equipment and use of vision QC spotting process and live monitoring of spotting equipment. Key duties: - The Lead Production Operator will be an advanced operator in carrying out all tasks associated with the Production Operator role and will be deemed highly competent in carrying out aspects of Production procedures, specialising in either: Spotting, Assembly, Buffer Formulation or a combination of the three. - The Lead Production Operator will be directed by, and report to - the Production Team Leader or Production Supervisor on daily tasks. (Refer to: Teo Biochip manufacturing organisational chart). - The Lead Production Operator will act as a reference point for Production Operators and Trainee Operators and will also be involved in the training of staff in Biochip/Assembly/Buffer Preparation processes. - The Lead Production Operator will be trained in the majority of aspects related to Biochip Formulation, and in the event of Team Leader absence, will be capable of acting as the Production Team Leader. - They will have added responsibility in the monitoring of critical aspects relating to the continued operation of the cleanroom areas, including: - Stock control/generation of purchase requisitions. - Ensuring productivity logs are maintained. - Trouble shooting and conveying pertinent issues to senior staff. Who can apply? Essential criteria: - Be qualified to GCSE level or have previous experience in a production or manufacturing environment. - Experience of working within a Clean room environment. - Computer literate and be confident in the use and application of Microsoft Office packages. - Good team working skills. - Possess excellent communication skills (written and verbal). - Possess good organisational skills. - Have the right to work in ROI. Desirable: - Working knowledge of Health and Safety procedures, including CoSHH. - Experience in working to quality systems. How do I apply? Apply on the site you are seeing this advert on, and they will submit your CV to our client for review. This advert may be open for as long as 30 days although they may close the advert early if they receive sufficient applicants to fill the roles. The Organisation: An international company operating in over 145 countries that continues to have unparalleled growth, our client was at the centre of the UKs National COVID Testing Programme throughout the pandemic. In early 2020, they recognised the threat from COVID-19 and based on over 40 years of diagnostic experience, quickly developed a test to accurately identify the virus. Testing at scale commenced within weeks to support the UKs National Testing Programme and private clients alike. Additionally, as a world leader in diagnostics for clinical healthcare, toxicology and food security, their expertise and product portfolio have assisted laboratories across the world in improving health and saving lives. Their global success is a result of their pioneering products and the commitment & skill of their workforce, which continue to grow exponentially. Central to our clients ethos is their drive and determination to improve healthcare worldwide and every one of their talented staff play a role in this. In order to serve their growing international markets, they require high calibre applicants with scientific, engineering, software, and broader business skills including sales, marketing, logistics, finance and many more. Join the team and play your part in improving the health of millions. Our client is an Equal Opportunities Employer.