8 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
We are looking for a QC Manager Projects to join our team on our Manorhamilton Road site in Sligo. The QC Manager Projects drives project-related activities within the QC department, focusing on the introduction of innovative analytical techniques, automation, and the transition to a paperless lab environment. This role is pivotal in the implementation of the "Lab of the Future" concept and managing lab expansion projects.
Responsibilities:
+ Lead and manage all project-related activities in the QC department.
+ Oversee the introduction of new analytical techniques, focusing on automation and paperless laboratory systems.
+ Manage the implementation of the Lab of the Future initiative in the QC department.
+ Coordinate and oversee laboratory expansion projects.
+ Ensure compliance with data integrity policies and regulatory requirements.
+ Liaise with cross-functional teams to facilitate project goals and timelines.
+ Participate in internal and external audits and address audit findings.
+ Present project updates and technical data to stakeholders effectively.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Experience working in API and OSD QC laboratories.
+ Minimum 4 years of experience in people management within a QC lab setting.
+ Strong project management, presentation, and communication skills.
+ Innovative thinking, with a commitment to advancing laboratory practices 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:

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
Aseptic Manufacturing Specialist
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X ( , Facebook, Instagram ( , YouTube and LinkedIn.
Job Description
We are currently looking for an Aseptic Manufacturing Specialist to join our team in AbbVie Ballytivnan, Sligo. This person will be responsible for defining and updating procedures for the site in relation to gowning, aseptic behaviours and contamination control strategy. This person will be an SME in sterility assurance, microbiological, environmental monitoring and contamination control topics and has the opportunity to have a positive impact on our growing site in Sligo.
+ Implement an effective and robust training and requalification program for isolator activities, Grade C and Grade D gowning and aseptic behaviours on site.
+ Provide governance and support for sanitisation programs on site.
+ Support the facilities sterility assurance program and microbiological support activities to ensure the facility design, equipment and filling process met aseptic requirements from design to end user.
+ Represent AbbVie Ballytivnan in aseptic governance for projects to ensure all requirements for aseptic processing, facility design and filling of sterile product are met as per regulatory and global requirements.
+ Support the EM and utilities program process, aseptic programme and contamination control strategy in a multiproduct facility.
+ Understand Regulations and business processes required to maintain AbbVie's and cGMP requirements for sterile product, inclusive of facility design, cross contamination controls and Data Integrity.
+ Define and update procedures for site relative to gowning, aseptic behaviours and contamination control strategy.
+ Carry out training as per training plan to support facility sterility assurance program.
+ Adheres to and supports all EHS & E standards, procedures and policies. EHS Responsibilities.
+ Comply with the EHS policy and procedures and demonstrate EHS best practices in all work activities.
+ Continually be conscious of your own safety and that of others, always complying with safety notices and barriers.
+ Report any EHS incidents and/or Near Misses (unsafe acts and conditions) immediately to your supervisor and always raise the event in eAchieve.
+ Support a culture of EHS excellence by recognizing and submitting opportunities for EHS improvement on eAchieve.
+ Wearing of PPE as required.
Qualifications
Qualifications
+ A thorough knowledge of aseptic and sterile processes together with experience within a GMP environment and knowledge of current EU/FDA/ICH/HPRA and Annex 1 guidelines.
+ 3 -5 years' (minimum) experience in microbiology is a requirement & working in a sterile/aseptic/pharma environment is a distinct advantage.
+ Experience in supporting regulatory inspections HPRA, FDA etc is an advantage
+ Bachelor Degree qualification in biology or microbiology
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
Join our dynamic TPM Management Group, a team dedicated to ensuring rigorous oversight of Third Party Manufacturing (TPM) operations for key late pipeline and newly commercialized products. Collaborate with stakeholders across Operations to drive excellence and efficiency in the manufacturing process.
In this role you will manage a team of Manufacturing Professionals assigned to Third Party Manufacture (TPM) contracts for small molecule products. You will assure that high quality product is manufactured in compliance with local and international regulations, and released and delivered according to the established forecasts, schedules, and cost planned.
Responsibilities
+ Lead a team of AbbVie TPM Account Managers to: Negotiate Manufacturing Service Agreement and amendments, and assure compliance with the terms of the agreements and Assure effective planning and material procurement strategies are in place to efficiently supply TPMs with required
materials.
+ Assure global logistics are in place to support all phases of the manufacturing agreement in accordance with Purchasing and Supplier quality expectations.
+ Ensure timely communication to the TPM in all aspects of the product agreement including product forecasts, manufacturing and delivery schedules.
+ Lead the development of Financial Operating Plan, Updates, LRP, and Standard processes, and assure the financial goals are met.
+ Monitor manufacturing performance; apply performance metrics as appropriate and ensure work processes and standards align to deliver product in accordance with AbbVie quality 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 QA, 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.
+ Lead a performance improvement culture & programs across TPMs; guide Account Managers to anticipate and act on ideas to increase efficiency and effectiveness.
+ Coach managers in the organization and establish clear expectations with them and all employees regarding responsibilities, goals and behaviours and champion and model exceptional AbbVie performance and talent management practices.
+ Coordinate routine management reviews and provide on-going communication informing internal and TPM stakeholders of TPM performance against expectations, highlighting issues, actions, and on-going improvements to increase performance at TPMs.
+ Represent Manufacturing as required with internal Brand Teams related to all aspects of the manufacturing process with TPMs and develop and manage staff through hiring, managing performance, developing talent and providing clear expectations.
Qualifications
+ Bachelor's Degree required in a technical field: advanced technical degree (Master's or Doctorate Degree) strongly
preferred.
+ 15+ years' experience including: work as an individual contributor building technical expertise and proven project
management skills.
+ Progressively increased responsibility and performance as supervisor, department manager and leader of diverse teams
in Operations (Manufacturing, Quality, Supply Chain, Engineering, etc.)
+ Business acumen coupled with functional leadership experience is required to ensure effectiveness and high performance in a complex operation.
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:

Our client, a leading manufacturing company based in Sligo, is seeking an experienced Manufacturing Engineering Manager to join their team on a full-time permanent basis.

Reporting directly to the Plant Manager, this newly created position will lead the Engineering Department, overseeing new product and process development, process optimization, continuous improvement initiatives, and environmental functions. The Engineering Manager will drive strategic investments in manufacturing equipment, tooling, and production systems, with a strong focus on "right-sizing" — ensuring optimal flexibility, minimal investment risk, and capitalizing on emerging technologies to support growth and innovation.

Key Responsibilities include but are not limited to the following:

• Act as the Strategic Manager across multiple technologies, overseeing all local site services (air, water, electricity).

• Develop and implement systems, procedures, and protocols in line with Quality Management Systems and Design Control standards.

• Ensure compliance with all Health and Safety, Environmental, and Quality regulations.

• Lead the development and execution of a comprehensive asset management system, incorporating all maintenance functions.

• Identify and select best-value technologies that align with operational goals.

• Prepare and manage annual operational and capital expenditure budgets.

• Oversee day-to-day team management, project resourcing, and hiring.

• Deliver profitable and timely product and project launches.

• Prioritize and drive the execution of complex engineering projects, promoting value improvements across the operation.

• Facilitate efficient transfer of process knowledge to manufacturing teams; coordinate training of production personnel on new equipment and processes.

• Foster a culture of continuous improvement in support of customer quality standards.

• Lead cross-functional collaborations to identify and resolve production and engineering challenges.

• Build, lead, and develop a high-performing engineering team, ensuring all operational, training, and health and safety standards are met.

• Degree in Engineering or a related discipline.

• 5+ years’ experience at a senior level within a manufacturing environment.

• Highly organized, motivated, and goal-driven individual with strong cross-functional collaboration skills.

• Proven expertise in project management and resource management within complex, high-volume manufacturing environments.

• Technically strong, numerate, with excellent analytical and problem-solving abilities.

• Quality-focused mindset with a "Right First Time" approach and strong attention to detail.

• Exceptional interpersonal, communication, and leadership skills, with the ability to engage effectively at all organizational levels.

• Strong people management skills and proven team leadership experience.

• Working knowledge of modern manufacturing technologies including plastic injection moulding, metal stamping, and automation.

• Solid understanding of technology deployment and continuous improvement methodologies.

• Familiarity with quality systems and standards, including PSW, PPAP, APQP, and Lean principles.

• Strong business and financial acumen with the ability to measure and improve operational effectiveness.

Immediate interviews available for suitable candidates.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other future vacancies.

 Pale Blue Dot® Recruitment

The Experts in STEM Workforce Solutions

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:

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
Join our dynamic TPM Management Group, a team dedicated to ensuring rigorous oversight of Third-Party Manufacturing (TPM) operations for key late pipeline and newly commercialized products that require Aseptic Manufacturing.
The Third-Party Manufacturing (TPM) Senior Manager will be the main supplier relationship contact person in charge of providing the organization, supervision, strategic initiatives, and technical support necessary to manage supply of designated products. The role will ensure that high quality product is manufactured in compliance with local and international regulations, and released and delivered according to the established forecasts, schedules, and cost planned.
This position also manages projects and programs impacting AbbVie to ensure a cost effective, marketable and manufacturable product and maximizes profitability throughout its life cycle. Through matrix management of cross functional groups/individuals, the Senior Manager, TPM is responsible for leading various teams without direct authority, providing program management support, and is the primary AbbVie representative to coordinate operations for existing and new products manufactured with the supplier.
Key Responsibilities:
+ Ensure effective planning and material procurement strategies are in place to supply the TPM with the required materials.
+ Participate in the negotiation of the Manufacturing Service Agreement and amendments and ensure compliance with the terms of the agreements.
+ To visit Third Party Manufacturer sites on a regular basis to increase engagement, with proactive in-plant assessments, identifying opportunities for safety, quality and process improvement
+ Communicate to the TPM the product forecasts and agree on manufacturing and delivery schedules.
+ In coordination with Supply Chain and Planning, ensure the supplier delivers the product according to the demand forecasted.
+ Actively participate in the development of Financial Operating Plan, Updates, LRP, and Standard processes, and ensure the financial goals are met
+ Coordinate the Steering Committee and monitor that the Virtual Operation Teams meet periodically to evaluate performance, address issues, and if necessary, escalate.
+ Review status reports and prepare updates for Senior leadership.
+ In collaboration with technical and quality teams, periodically review process performance, quality trends, and agree on process improvement plans.
+ Establish governance, guidelines, and communication channels. Ensure in coordination with the quality units that the supplier has the required quality systems and documentation to meet regulatory requirements, follow up inspection responses and commitments.
+ Coordinate with QA, the annual quality management review and periodic audits of the TPM. Ensure deviations are properly investigated and product disposition decisions are made in a timely manner.
+ Establish performance metrics and periodically track performance.
+ Develop, implement and manage the programs or projects such as scope, cost, time & resource management, communication and risk management through the initiating, planning and executing phases of the project.
.
Qualifications
+ Bachelor's Degree, preferably in science or technical related field. MSc or MBA degree is preferred.
+ A minimum of 10+ years of experience, in areas such as manufacturing, engineering, project management, quality and S&T. Ideally, with direct experience of Aseptic manufacturing.
+ The individual needs a broad business perspective, knowledge and understanding of manufacturing processes.
+ Strong project experience and an ability to influence others are essential.
+ Previous experience managing subcontracted relationships preferred.
+ Proven leadership ability with superior communication skills including listening, verbal, presentation and written.
+ Strong strategy development and planning skills coupled with necessary knowledge of pharmaceutical development, manufacturing and supply activities.
+ Issue identification and strong problem analysis and solution development skills.
+ Demonstrated team player and ability to work in a globally oriented work environment.
+ Strong knowledge of business financial systems and tools
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: