7 Manufacturing jobs in Sligo

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
Join our dynamic team at AbbVie Ballytivnan (Sligo) and be part of groundbreaking work in Antibody Drug Conjugation (ADC).
As a Team Lead in our Biologics division you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, and build an inclusive culture of high performance for the team.
+ Lead and manage the operations team, ensuring adherence to safety, regulatory, and operational requirements.
+ Foster a high-performance culture focused on customer service, quality, compliance, financial performance, and inclusion.
+ Oversee and execute filling, lyophilization, equipment preparation, formulation, buffer preparation, and support processing activities.
+ Prioritize safety and compliance in all activities, conducting regular safety Gembas and promoting a culture of zero safety incidents.
+ Review daily work activities to identify and address high-risk activities.
+ Ensure compliance with EHS standards, procedures, and policies.
+ Promote a culture of contamination control and adherence to aseptic best practices.
+ Effectively deploy and manage team members to meet production schedules.
+ Provide daily reporting on the status of operations and support activities.
+ Lead, motivate, and direct the manufacturing team to maximize effectiveness.
+ Foster team engagement through regular one-on-ones, clear expectations, feedback, performance reviews, and action plans.
+ Develop direct reports through training, challenging tasks, and performance reviews.
+ Promote a culture of Right First Time execution, Behavioral Based Safety, Always Audit Ready, and Human Error Reduction.
+ Drive operational excellence and achieve key operations targets, including OEE.
+ Ensure compliance with safety, environmental, and quality-related SOPs.
+ Collaborate with other Technical Shift Leaders for interdepartmental planning and execution.
+ Schedule human and material resources to meet production schedules.
+ Utilize management infrastructure tools, trackers, visual management, tier meetings, and Gemba walks.
+ Ensure smooth shift handover and communication of performance metrics.
+ Identify and supervise critical process steps during your shift.
+ Achieve financial targets by improving overhead spend, material usage, and labor efficiency.
+ Manage cycle time and identify improvement opportunities.
+ Collaborate with program management, supply chain, technical operations, quality, and engineering for effective planning, scheduling, and execution.
+ Provide technical guidance and approval for manufacturing batch records.
+ Verify and update manufacturing control system transactions accurately and timely.
+ Serve as the key technical contact for aseptic fill-finish activities.
+ Support the documentation and investigation of NCRs.
+ Interface with QA department for interactions with HPRA, FDA, and other health authorities.
+ Lead cross-functional risk assessments and continuous improvement projects.
+ Compile and analyze data to track process performance.
+ Provide technical expertise for investigations, root cause analysis, CAPAs, process improvements, and change control reviews and approvals.
+ Manage compliance issues that may arise during shifts and ensure adherence to regulatory requirements.
Qualifications
+ Degree, Masters or PhD in Life Sciences, Process Engineering, Biopharmaceutical Engineering or Chemical Engineering discipline
+ A minimum of 5 years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
+ Has a technical background in pharmaceutical, biologics, or similar industries
+ Experience of start-ups and/or new product introductions to bio-pharmaceutical/pharmaceutical facilities (Biologics Preferred). Must be able to lead & project manage these activities.
+ Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality and safety requirements.
+ A minimum of 1 year team direct supervisory experience in a team environment
+ Possesses a strong technical knowledge and application of concepts, practices, and procedures.
+ Works on problems of complex scope where analysis of situations or data involves multiple competing factors.
+ Exercises judgment and advises management as to the appropriate actions. ·
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:

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
*Please note that job level/grading my differ from country to country*
Purpose
Manage a team of Manufacturing Professionals responsible for Third Party Manufacture (TPM) contracts for Medical Devices or Combination Products. Assure that high quality products are manufactured in compliance with local and international regulations, and released and delivered according to the established forecasts, schedules, and cost planned. On going monitoring quality and delivery performance while minimizing risks associated with outsourcing production to a Third-Party Manufacturer.
Responsibilities
+ Lead a team of AbbVie TPM Account Managers to: Negotiate and manage Manufacturing Service Agreements (MSA), contract Amendments, and updates as needed, while ensuring compliance with the terms of the agreements. Asure global logistics are in place to support all phases of the manufacturing agreement in accordance with Purchasing and Supplier Quality expectations.
+ Lead the development of ECM Device Financial Operating Plan, Updates, LRP, and Standard processes, and assure the financial goals are met. Monitor and control manufacturing costs to ensure efficient use of resources while maintaining product quality.
+ Ensure timely communication with TPM in all aspects of the product agreement including product forecasts, manufacturing and delivery schedules. Identify, evaluate, and maintain strong relationships with third-party manufacturers to ensure quality production and timely delivery.
+ Monitor manufacturing performance; apply OPEX (Operational Excellence) metrics as appropriate and ensure TPM manufacturing processes and standards align to deliver product in accordance with AbbVie quality & performance expectations.
+ Assure in coordination with internal AbbVie functional partners that the TPM has the required quality systems and documentation to meet regulatory requirements, follow up inspection responses and commitments. Coordinate with PQA, the annual quality management review and periodic audits of the TPM. Assure deviations are properly investigated and product disposition decisions are made in a timely manner.
+ Coordinate routine management reviews and provide on-going communication informing internal and TPM stakeholders of performance against expectations, highlighting issues, actions, and on-going improvements to increase performance at TPMs.
+ Identifying and Selection of Third-Party Manufacturers (TPM); ensure team engagement on cross functional evaluation of new product needs and TPM's due diligence initiatives.
+ Identify, evaluate, and maintain strong relationships with third-party manufacturers to ensure quality production and timely delivery from onboarding, contract negotiations though renewals of the TPM.
+ Identify potential disruptions like geopolitical instability, natural disasters, or labor issues and develop mitigation strategies.
+ Ensure the manufacturer adheres to all relevant regulations regarding safety, environmental standards, and labor practices.
+ Foster a collaborative partnership with TPMs to ensure mutual understanding and commitment to quality & performance.
+ Lead a performance improvement culture & programs across TPMs; guide Account Managers to anticipate and act on ideas to increase efficiency and effectiveness.
+ Establish and manage clear team expectations regarding roles & responsibilities, G&O's while champion and model AbbVie's performance and talent management practices.
+ Develop and manage staff through hiring, managing performance, developing talent and providing clear expectations.
Qualifications
Qualifications
+ Bachelor's Degree required in a technical field: advanced technical degree (Master's or Doctorate Degree) strongly
preferred.
+ 15+ years' experience including: manufacturing of Medical or Electro-Mechanical Devices
+ Strong technical and manufacturing assembly management experience
+ Progressively increased responsibility and performance as supervisor, department manager and leader in Operations (Manufacturing, Quality, Engineering, etc.) Proven ability to inclusively manage and develop teams.
+ Strong communication skills, ability to build trust and rapport, clear goal setting, fostering collaboration, promoting creativity, and adapting leadership style to suit the team's needs.
+ Business acumen coupled with functional leadership experience is required to ensure effectiveness and high performance in a complex operation.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
+ This job is eligible to participate in our long-term incentive programs

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

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:

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects. Visual Inspection Engineer Responsibilities: To work as a team member to support Visual Inspection operations in line with all safety, regulatory and organizational requirements. Develop and modify procedures as needed to support the manufacturing operation. Participate in process, equipment, and facilities validations efforts and projects implementations. Review and approve process related commissioning, qualification and validation protocols for completeness and accuracy. Execute protocols in a timely basis to meet the project schedule requirements. Participate and lead (as required) Process FMEAs for Visual Inspection Establish, Lead and Optimize the process for certification of technicians for visual inspection. Establish and maintain the defect library. Establish and execute the process for the trending of Visual Inspection Defects. Ensure all Site Visual Inspection procedures are aligned with Global Guidance Documents and Regulatory Requirements Provide Technical Input to guide the development of SOPs for Visual Inspection. Leadership of manufacturing and validation activities during project life cycle. Coordination with internal/external stakeholders for the evaluation of particles/defects Support of technical transfers for future product introductions to the site. Investigate process exceptions or malfunction incidents affecting the process. To liaise with Internal/External Engineering Personnel and Internal/External Quality personnel as required Support the Production Team in ensuring that manufacturing process is enabled and maintained to meet the output and yield requirements. Requirements: A relevant third level qualification in an engineering, science or technical discipline (Degree Level or Masters Preferable) At least three (3) years of total combined experience in Technical/Operations/Operations/Quality or equivalent in a Pharmaceutical and Health Care Organization. At least three (3) years of experience in the manufacturing environment of a biotechnology, pharmaceutical or health care plant. Previous experience in manufacturing processes of biotechnological drugs, parenteral drugs, solutions preparation, fill finish, Lyophilisation, sterilisation operations preferable. Experience in clean utilities is desirable. To start the process click the Continue to Application or Login/Register to apply button below.

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
If you want to be a difference maker our people are waiting. See the difference you can make at AbbVie.
Working at AbbVie is more than a job. It's a career with meaning. A chance to make a difference, in the world and in your life.
We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thrive-at AbbVie and beyond.
Join our dynamic team at AbbVie Ballytivnan (Sligo) and be part of groundbreaking work in Antibody Drug Conjugation (ADC).
As a Team Lead in our Biologics division you will assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, and build an inclusive culture of high performance for the team.
+ Lead and manage the operations team, ensuring adherence to safety, regulatory, and operational requirements.
+ Foster a high-performance culture focused on customer service, quality, compliance, financial performance, and inclusion.
+ Oversee and execute filling, lyophilization, equipment preparation, formulation, buffer preparation, and support processing activities.
+ Prioritize safety and compliance in all activities, conducting regular safety Gembas and promoting a culture of zero safety incidents.
+ Review daily work activities to identify and address high-risk activities.
+ Ensure compliance with EHS standards, procedures, and policies.
+ Promote a culture of contamination control and adherence to aseptic best practices.
+ Effectively deploy and manage team members to meet production schedules.
+ Provide daily reporting on the status of operations and support activities.
+ Lead, motivate, and direct the manufacturing team to maximize effectiveness.
+ Foster team engagement through regular one-on-ones, clear expectations, feedback, performance reviews, and action plans.
+ Develop direct reports through training, challenging tasks, and performance reviews.
+ Promote a culture of Right First Time execution, Behavioral Based Safety, Always Audit Ready, and Human Error Reduction.
+ Drive operational excellence and achieve key operations targets, including OEE.
+ Ensure compliance with safety, environmental, and quality-related SOPs.
+ Collaborate with other Technical Shift Leaders for interdepartmental planning and execution.
+ Schedule human and material resources to meet production schedules.
+ Utilize management infrastructure tools, trackers, visual management, tier meetings, and Gemba walks.
+ Ensure smooth shift handover and communication of performance metrics.
+ Identify and supervise critical process steps during your shift.
+ Achieve financial targets by improving overhead spend, material usage, and labor efficiency.
+ Manage cycle time and identify improvement opportunities.
+ Collaborate with program management, supply chain, technical operations, quality, and engineering for effective planning, scheduling, and execution.
+ Provide technical guidance and approval for manufacturing batch records.
+ Verify and update manufacturing control system transactions accurately and timely.
+ Serve as the key technical contact for aseptic fill-finish activities.
+ Support the documentation and investigation of NCRs.
+ Interface with QA department for interactions with HPRA, FDA, and other health authorities.
+ Lead cross-functional risk assessments and continuous improvement projects.
+ Compile and analyze data to track process performance.
+ Provide technical expertise for investigations, root cause analysis, CAPAs, process improvements, and change control reviews and approvals.
+ Manage compliance issues that may arise during shifts and ensure adherence to regulatory requirements.
Qualifications
+ Degree, Masters or PhD in Life Sciences, Process Engineering, Biopharmaceutical Engineering or Chemical Engineering discipline
+ A minimum of 5 years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.
+ Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
+ Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
+ Has a technical background in pharmaceutical, biologics, or similar industries
+ Experience of start-ups and/or new product introductions to bio-pharmaceutical/pharmaceutical facilities (Biologics Preferred). Must be able to lead & project manage these activities.
+ Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality and safety requirements.
+ A minimum of 1 year team direct supervisory experience in a team environment
+ Possesses a strong technical knowledge and application of concepts, practices, and procedures.
+ Works on problems of complex scope where analysis of situations or data involves multiple competing factors.
+ Exercises judgment and advises management as to the appropriate actions. ·
Additional Information
You're here to make a difference. We have the science to turn you into difference makers.
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
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.
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
We are looking for a QC Manager to join our team on our Manorhamilton Road site in Sligo. The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD products, and coordinating with internal teams to meet testing schedules.
Responsibilities:
+ Manage a lab team performing QC testing, ensuring compliance with data integrity policies and regulatory requirements.
+ Conduct and supervise all aspects of API and OSD analytical testing.
+ Ensure timely sampling, inspection, and testing, coordinating with teams for schedules and priorities.
+ Participate in internal and external audits and address audit findings.
+ Prepare technical reports, lead investigations, and implement CAPAs.
+ Provide training and support to lab team to achieve daily and long-term goals.
+ Present technical data to stakeholders to facilitate prompt decision-making.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Minimum 4 years of experience in people management within a pharmaceutical lab setting.
+ Strong knowledge of QA/QC operations, analytical testing for API and OSD.
+ Excellent presentation and technical report writing skills.
+ Strong communication and interpersonal skills, with a commitment to quality and compliance.
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: