21 - 30 of 78 Jobs 

Reliability / Manufacturing

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Want to make a global impact? We offer that Ready to innovate? We offer that too Welcome to AbbVie! AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people and, when we find them, we make it our business to treat them well. We are currently sourcing an experienced Reliability Engineer/Process Engineer to join our high performing Maintenance and Engineering in Westport - interested? then read on.... In this role, you will: • To provide technical support for the aseptic filling, lyophilization, inspection and packaging of biological drug product. • Act as technical expert / SME on reliability engineering on site • Subject Matter Expert (SME) in the aseptic filling process, isolator technology, packaging equipment, automated inspection and representation at various regulatory audits. • Understand the Biologics process by evaluating process and technical data, literature, and work closely with E&T dept. • Support process investigations, primarily by seeking a technical root causes and liaise with cross functional departments to perform investigations if required. • Facilitate and lead the MEP RCM & RCA program on-site; using Lean Tools to identify the root cause of problems and implement effective actions to ensure non-recurrence • Deliver maintenance systems improvements and identify technical/financial improvement opportunities • Actively work with the Maintenance & Projects Team to ensure the MEP Program and site is QA & EHS Compliant and Audit ready • Assist with product impact assessment for change controls and internal/external investigations as required. • Monitoring and analysis of process data during the manufacturing and packaging of drug product. • Identification and project management of continuous improvement projects. Work closely with other departments to deliver these continuous improvement projects. • Continuously drive to improve processes for improved performance and cost reduction wherever possible • Take ownership for reliability standards within the department (equipment, processes, systems, and utilities) Qualifications Still interested? for this role, you will have Education & Experience • Degree qualified in Engineering or relevant experience • Minimum of 3 years experience in pharmaceutical process/reliability engineering, with relevant experience of batch processing, commissioning and validation in a cGMP pharmaceutical or Biologics industry • Experience in new product introductions to Biologic facility is desirable • Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements are required • Experience working with lean methodologies is desirable. • Previous experience in lyophilization and sterilization operations preferable • Strong competency on IT systems and documentation processes. • Able to think strategically and creatively, and to establish and maintain relationships with key stakeholders and cross-functional teams. So, are you ready now to be part of this innovative Maintenance & Engineering team? then apply today! It’s important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

30+ days agoFull-time

Pharmaceutical Technology Specialist II

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Want to make a global impact? We offer that Ready to be part of a team focused on innovation? We offer that too Welcome to AbbVie! AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people and, when we find them, we make it our business to treat them well. We are currently recruiting Pharmaceutical Technology Specialists to join our high performing innovative Pharmaceutical Technology team in Westport. In this role, you will be responsible for all manufacturing activities necessary to support the tech transfer of a New Product Introduction (NPI) to accommodate clinical manufacture of a small and large molecule products within our manufacturing area. In this role, you will perform all manufacturing activities associated with the operation of the Biologics Development Manufacturing area while supporting activities for Biologics R&D and Pharmaceutical Technology (PT). Manufacturing duties can be broken into four distinct groups - Manufacturing (Clinical, Engineering, Development & Stability), Process Development, Biologic Drug Product commercial support New Product Introduction/ Project Management. Does this sound like the right next career move for you? here is a snapshot of the day-to-day activities: You will Be responsible for all aspects of drug product manufacture in the area - this includes all batch preparation activities (vial washing, load sterilization, area preparation), compounding, sterile filtration and sterile filling. Have a clear understanding around New Product Introductions (NPI) and the different requirements relating to each unique product. Be proficient in the use of single use technologies – understand the requirements around them and also be capable of working with the various vendors on the development/improvement of new/existing systems. Support the manufacturing of clinical, non-clinical and pre-clinical material in compliance with site and GMP procedures, ensuring that there is no disruption of clinical supply and that project milestones are met. Qualifications So, what education & experience do you need? You will have a relevant 3rd level qualification in a scientific discipline or chemical engineering with minimum 1 year + cleanroom experience Experience with prefill syringe technology preferred You need to be a strong trouble shooter, keen to learn with industry experience in NPIs and experience with commercial & / or clinical manufacture. You will have experience with single use technologies and an understanding of autoclave sterilization, dehydrogenation, filter integrity testing essential So, are you ready now to be part of this innovative diverse Pharmaceutical Technology team? join AbbVie! It’s important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

30+ days agoFull-time

Associate Documentation Analyst

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Want to join an award winning team? We OFFER that. Ready to make a Worldwide impact? We OFFER that too. Welcome to AbbVie! At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that's felt within healthcare and beyond. We are now recruiting a Associate Documentation Analyst for a 9 month contract to join our diverse Quality Assurance team in Westport. Associate Documentation Analyst is a member of the Document Control Department. The Document Control department in turn forms part of the QA group locally. The Document Control group is responsible for the processing of all One Vault Documentation for the Westport site. Document Control must maintain compliance with local, regulatory and legislative requirements with regards to Safety, Housekeeping, GMP and support and comply with internal environmental health and safety requirements, procedures and policies. It achieves these functions by interaction with QA, EHS, Compliance and regulatory affairs to ensure all internal procedures reflect current requirements. *So let’s tell you a little more about this role… Key Responsibilities: Monitor and coordinate content development across all manufacturing workstreams. Redline and update/obsolete SOPs, Controlled Forms, Project Documents and Manufacturing Records relating to the OMI project and submit on One Vault for Processing. Process above documents from Draft to Effective/Obsolete on One Vault as per internal procedures. Initiate training on all SOPs using LMS/Compliance wire system. Update and distribution of internal department documentation when necessary Run One Vault and LMS reports relating to department and other departments as required. Maintain all current KPI metrics at or above targets. Ensure Document Control is in compliance with all procedures at all times. Deal with Internal and External customer queries under the guidance of the department Supervisor. Qualifications Education: Proven track record in a quality discipline in the Pharma/Medical Device environment. Microsoft Office Word and Excel is essential. Clear understanding of working within a regulated environment Excellent communication skills Ability to use sound judgment to make effective decisions within appropriate timeframes. So, does this all sound like the right role for you? Then come join Abbvie! AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

30+ days agoFull-time

Service Manager

Dunnes StoresCastlebar, Mayo

Part Time Service Manager - Castlebar We are Ireland’s largest retailer providing fashion, homewares and food for our loyal customers. We operate 134 stores across Ireland, Northern Ireland, and Spain, as well as a growing online store. Our guiding principle is to deliver excellent quality products at competitive prices and we are constantly developing our product ranges.  We currently have a vacancy for a Part Time Service Manager. As a Service Manager you will learn about the business while developing your product knowledge and people management skills. As part of the management team within your store, you will also ensure that our standards of customer care are maintained and improved on an ongoing basis. This position is 120 hours per month, scheduled between 3 to 4 days per week, which will include late nights and weekends. The successful candidate will have the following responsibilities: Key Responsibilities: If this sounds like the job for you, please apply now and tell us why you would be perfect for this challenging and rewarding role! Dunnes Stores is an Equal Opportunities Employer #DunnesStores

30+ days ago

Laboratory Technician IV

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Want to make a worldwide impact? Want to join an award-winning team? Then join AbbVie! We focus on innovative new technologies, and with our high performing team, we develop and deliver products and processes to support AbbVie’s wider global needs. We are always looking for talented people to join our team and, when we find them, we make it our business to treat them well. We are currently sourcing a Laboratory Technician (Microbiology) to join our team at AbbVie, Westport Co. Mayo, on a fixed-term contract basis. As our new Lab Technician, you will carry out routine/non routine microbiology laboratory activities including environmental monitoring of cleanrooms; microbial analysis of site utilities and testing of raw material, commercial, clinical and development batches. As part of your role, you will manage the microbial analysis of AbbVie products included in the Global Stability program and show competence to ensure that the Microbiology function adds to the greater benefit of the facility from a Microbial control perspective. In association with the Microbiology Supervisors/Managers you will work to meet company goals and objectives, customer requirements and regulatory obligations as laid down by the FDA, EU and regional MOH. So, are you ready to join the AbbVie team? Then read on In your new role you will: • Maintain strong relationships with management and colleagues both within the Microbiology Lab and with associated Business units. • Articulate the necessary training/results in a clear, concise, and credible manner. • Actively participate in the training and certification of employees, safety, and quality initiative teams. • Ensure testing and monitoring is performed, results entered and validated as per determined schedules and in line with regulatory requirements • Ensure effective recording, analysis and reporting of Micro testing results ensuring issues impacting quality performance are addressed and drive continuous improvement. • Attend Departmental and OPEX meetings, Safety & Quality initiative Meetings and other meetings as directed • Provide review of Lab notebooks and documents. • Work directly with other Micro technicians to ensure that all testing is completed as per schedule. • Ensure appropriate investigation is performed on out of limit results from testing. • Ensure timely review of data generated within the team in conjunction with team reviewers. • Demonstrate active support and involvement in successful progress of compliance initiatives to enhance the site’s aseptic quality program. • Foster an environment of continuous improvements for the QC area by identifying and implementing efficiencies and quality improvements. Qualifications Qualifications • 3rd Level Qualification in Microbiology or equivalent scientific degree • Ability to articulate clearly when dealing with personnel • Relevant industry experience preferred. • Good oral, written, and presentation skills • Proven to be self-directed, self-motivated and ability to prioritize competing priorities AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Temporary Work Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

30+ days agoFull-timeTemporary

Maintenance Planner

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Challenging work with a global impact? We OFFER that. A rich innovative pipeline? We OFFER that too. Welcome to AbbVie! At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that's felt within healthcare and beyond. We are now recruiting a Maintenance Planner to join our diverse MDI Tech team in Westport, Co. Mayo. In this role, you will be responsible in facilitating the smooth and efficient operation of the maintenance function by assisting the maintenance personnel to meet the demands of the business and the associated targets. As part of your role, you will support maintenance excellence by planning maintenance activities using the company’s computerized maintenance management systems (CMMS). So let’s tell you a little more about this role… In your new role, you will: • Lead and execute the Maintenance Planning program of site equipment and utilities • Support the maintenance technicians with planning and preparing for the equipment maintenance to be performed by having the necessary tools, materials and EHS related permits needed • Implement programs and procedures required to ensure plant maintenance is performed in a compliant manner • Maintain a maintenance management system for tracking work orders, spare parts, and maintenance history of plant equipment • Track, analyze and improve key Maintenance Excellence Program (MEP) key performance indicators (KPI’s) parameters such as asset utilization, maintenance cost, site maintenance compliance, schedule etc. • Ensure adherence to company safety standards, policies, and procedures • Build and maintain strong partnership with the EHS function to ensure both the safety of staff and contractors is seen as paramount on site So does this role sound exciting? then read on..... Qualifications Qualifications To succeed in this role, you will have the following Education and Experience: Degree plus 1 years industry experience or Leaving Certificate plus 5 years in the education/experience area Knowledge of SAP/Maximo Experience working in a cGMP environment & pharmaceutical industry Strong IT Skills (MS Word, Excel, Access, Outlook) So, does this all sound like the right role for you? Then join AbbVie! As an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

30+ days agoFull-time

Sr Microbiologist

Charles RiverBallina, Mayo

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. We are seeking an experienced Senior Microbiologist for our Biologics Department located in Ballina, Co. Mayo. You shall be reporting to the Microbiology Department Manager. The main duties & responsibilities shall be; About Biologics Testing Solutions With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2018.

26 days ago

Microbiologist

Charles RiverBallina, Mayo

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. Job Spec We are seeking an experienced Microbiologist for our Biologics Department located in Ballina, Co. Mayo. You shall be reporting to the Microbiology Functional Manager. The main duties & responsibilities shall be; About Biologics Testing Solutions With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017. At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of ~85% of the drugs approved by the FDA in 2018.

26 days ago

Engineering Director

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Want to invest in your leadership career? We offer that Be part of a diverse senior leadership team? We offer that too Welcome to AbbVie! AbbVie employees work every single day to discover and address many of the world's most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions, you look for the best people and, when we find them, we make it our business to treat them well. We are currently sourcing a hardworking Engineering Director to lead our committed, innovative engineering team in AbbVie, Westport, Co. Mayo in achieving global manufacturing excellence. Reporting to the Site Director, this position has been identified as a key talent development role that will be leveraged to identify future leaders for local and international career opportunities. You will be interfacing with the global engineering group and as part of the site senior leadership team, delivering on our key strategic initiatives, influencing site financial growth and business decisions. You will be responsible for all Engineering aspects associated with an aseptic fill-finish production facility (covering Aseptic manufacture of Biologic, Eyecare and Implant Drug Products), be accountable for delivering high performing process and utility equipment, ensuring a best-in-class compliant facility to meet the stringent demands of modern Aseptic Fill-Finish processing and for providing Department leadership and direction in the areas of Process Engineering, Maintenance, Aseptic Engineering, Capital Project Engineering, Environmental Sustainability, Site Security, Business Continuity Planning, Automation and Business Technology. Does this sound like the right next leadership move for you? then read on.... Here is a snapshot of your responsibilities: Delivery of the required Safety, Environmental, Quality and Financial performance of the Engineering Department. Partnering with the Site Leadership Team, ensure that the Site meets its Safety, Environmental, Quality, Customer Service and Financial goals through the effective management of plant resources. Lead high performing cross-functional and/or matrix teams, creating a positive employee engagement culture aligned to the AbbVie Way. Accelerate the development of key talent. Build relationships across the organization. Ensure the safety of our employees through provision of a safe workplace and showing leadership in the ‘Zero, Believe It, Achieve It’ Cultural Safety initiative. Ensure Qualification status of all Equipment is maintained. Ensure optimum equipment design and set-up from an Aseptic perspective. Ensure top-tier equipment reliability through the AbbVie Maintenance Excellence Program. Deliver the approved Capital Investment plan, including all aspects of planning and execution. Ensure delivery of Engineering projects on time and within budget; Ensure alignment of Site Leadership Team on priority projects which deliver site and enterprise strategic imperatives. Develop and implement projects to support the introduction of New Products. Develop annual capital Long Range Plan (LRP) to support any investments required to maintain or increase capacity and capability. Lead the Business Continuity Plan for the site. Lead the Site Automation team, ensuring delivery of all objectives. Be the point of contact for Business Technology Systems (BTS), ensuring a strong partnership to deliver on site objectives. Lead Environmental Sustainability initiatives for the site including maintaining ISO 50001 Registration through strategic long range planning, project identification and execution, management of Energy Team, Quarterly Reviews, energy monitoring and analysis Developing and executing the site Environmental Sustainability Long Range Plan Lead the provision of Site Security services. Ensure maintenance and upkeep of site buildings, internal and external. Ensure contractor compliance with all relevant legislative and company requirements/procedures. Qualifications Still interested? for this role, you will have Bachelor’s degree in Electrical, Mechanical or Chemical Engineering (Masters an advantage) 10+ years of Engineering and/ or Operations experience (Large Molecule, Small Molecule, Biologics, Parenteral, API, Drug Product, Finishing/Packaging) Demonstrated leadership, coaching, and mentoring of diverse teams Excellence in cGMP and regulatory environments relating to the regulated healthcare industry, project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements Ready for your next move? then apply today! AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel No Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

26 days agoFull-time

Senior Manager Analytical Development

AbbvieWestport, Mayo

About AbbVie AbbVie’s mission is to discover and deliver innovative medicines 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, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Unleashing your full potential? We OFFER that. A career of limitless possibility? We OFFER that too. Welcome to AbbVie! At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that's felt within healthcare and beyond. We are now recruiting a Senior Manager Analytical Development to join our diverse Pharmaceutical Technology team in Westport, Co. Mayo. In this role you will be responsible for all Analytical activities for ongoing R&D Products, Biologics MPS Analytical and all New Product Introductions into the Biologics Pharm Tech Group. You will manage the GPT Analytical teams (WBDL, NPI Analytical and MPS) on the various activities of each NPI/Ongoing Product to implement all analytical requirements throughout the life cycle of the product and to support all products into commercial. This will require skilled analytical personnel. You will be responsible for leading all analytical teams within the GPT function and must be able to liaise with multiple sites and departments across the network to ensure product transfers and submissions. So let’s tell you a little more about this role…just a snapshot In your new role, you will: Lead, coach, mentor and develop your team, building their capabilities and helping them advance their technical & analytical aptitude Liaise with multiple sites and departments across the network to ensure product transfers and submissions Project manage all Biologic NPIs Biologics MPS Analytical management Routine Product Testing -Release and Stability Provide technical support to all aspects of analytical activities, in accordance with site SOPs and multiple product controls Review/Approval of all analytical/product documentation Support installation of new equipment as required Review/Approval of quality records in QMS Support Budgets and yearly R&D Tax Credits technical documents Support regulatory inspections as required Qualifications So does this role sound exciting? then read on..... To succeed in this role, you will have the following Education and Experience: • Bachelor’s degree required with minimum 3-5 years management experience • Minimum of 8 years in a relevant environment with applicable experience • Excellent organizational and time-management skills and respond appropriately to numerous requests and prioritize accordingly, within tight deadlines to deliver NPI/Product lifecycle activities on time and within compliance So, does this all sound like the right role for you? Then join AbbVie! As an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment. Travel Yes, 5 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

26 days agoFull-time
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