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QC Lab 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 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 QC Lab Analyst to join our team at AbbVie, Westport Co. Mayo, on a fixed-term contract basis. As our new QC Analyst, you will ensure that all raw material, in-process, finished product and method transfer testing is carried out per schedule and records are maintained to appropriate requirements. Working in the quality control labs, you will be equipped with the latest design technology for chemical and microbiological analytical testing to meet customers’ needs. So, are you ready to join the AbbVie team? Then read on Key Responsibilities: Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements. Understand Regulations and business processes required to maintain Laboratory Data Integrity. Responsible for the timely completion of chemical testing. Ensure that all test equipment is used and maintained correctly. Raise change requests and data verification as assigned. Ensure all in-process sampling and testing is completed on time. Maintain up-to-date, complete and precise records of all tests performed. Adhere to cGMP and GLP requirements. Assist in the resolution of quality problems as required. Develop in-house laboratory procedures as appropriate. Support the transfer of new products. Adhere to and supports all EHS & E standards, procedures and policies Qualifications Education 3rd level degree qualification in relevant scientific discipline. Experience using HPLC/GC analytical methods is essential. Relevant industry experience preferred. Good oral, written, and presentation skills Strong analytical skills, ability to analyze data and trends and draw conclusions 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-timeTemporary

Quality Systems 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. Unleashing your full potential? We OFFER that. Rewarding career with ongoing professional development? 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 worldwide. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact felt within healthcare and beyond. We are now recruiting a Quality Systems Analyst at our Westport Site in Mayo on a 1-year fixed-term contract basis. In your new role, you will join a talented project team as part of the MSTU project to deliver the Windows 10 upgrade on laboratory systems, identifying gaps, planning interim actions and remediations inclusive of evaluating data integrity. So, if you are ready to make a significant impact with your next role and want to be part of an exciting project, read on to find out more and get your application started today! Key activities: Advising project team on related topics including data management and control. Generating and managing non-conformance records in Global TrackWise. Understanding and advising on change control and change management. Managing changes and maintaining existing Laboratory systems in a validated state. Supporting existing quality systems and aiding in the investigation/resolution of issues as they arise. Working on new systems planning phases to include defining processes. Assessing the Risk associated with changes. Partaking in Vendor consultation & functional specification definition. System configuration and supporting re-qualification. Writing and reviewing SOPs, test protocols and reports. Completing user access reviews and delivering training to end-users. Working in a cross-functional capacity between BT and the Laboratories SMEs to ensure planned and unplanned systems downtime does not impact business function. Assisting the Project Manage Team in identifying opportunities for improvement and delivery efficiency. Qualifications Education and Technical Skills: Degree qualified in relevant scientific discipline. Extensive knowledge of laboratory systems, ideally including validation testing, commissioning and decommissioning. Knowledge of computer systems pertinent to role preferred. Proven track record in quality systems configuration/validation implementation OR support. Knowledge of DI and CSV regulatory standards and compliance requirements with an emphasis on European and US regulatory environments. Excellent communication skills. Ability to use sound judgment to make effective decisions within appropriate timeframes. Proven to be self-directed, self-motivated, and able to prioritise competing priorities. So, if all this sound like the right role for you, then apply today! The closing date for the application is the 8th of Oct. 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-timeTemporary

Snr Cost Accountant

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. Ongoing learning and development? We offer that. Fantastic work-life balance? We offer that too. Welcome to AbbVie! Our employees work every day to discover and address many of the world's most pressing health challenges. When you have patients depending on your solutions, you look for the best people to join the team. We now have an opportunity for a Senior Cost Accountant Analyst to join our Westport team on a fixed-term contract basis. In this position, you will help create and maintain plant standard costs in SAP for the global internal and external manufacturing network. As a subject matter expert for global Operations SAP financial and costing functions, you will help ensure consistency and optimise cost accounting practices across the AbbVie plant network. Does this sound like an exciting role? Then read on and come join the AbbVie team! Key responsibilities: Create and maintain standard costs in SAP across manufacturing plants with the AbbVie Europe network. Support holistic analysis of plant information by creating reports that consolidate spend and volume data from SAP. Provide critical data and support to site finance business-facing teams. Promote process standardization throughout the plant network, including Budgets, Forecast, LRP and Month End Reporting. Actively seek practices that will improve accounting processes and efficiencies. Ensure compliance with relevant governmental agencies, EHS and quality. Qualifications Ongoing learning and development? We offer that. Fantastic work-life balance? We offer that too. Welcome to AbbVie! Our employees work every day to discover and address many of the world's most pressing health challenges. When you have patients depending on your solutions, you look for the best people to join the team. We now have an opportunity for a Senior Cost Accountant Analyst to join our Westport team on a fixed-term contract basis. In this position, you will help create and maintain plant standard costs in SAP for the global internal and external manufacturing network. As a subject matter expert for global Operations SAP financial and costing functions, you will help ensure consistency and optimise cost accounting practices across the AbbVie plant network. Does this sound like an exciting role? Then read on and come join the AbbVie team! Key responsibilities: Create and maintain standard costs in SAP across manufacturing plants with the AbbVie Europe network. Support holistic analysis of plant information by creating reports that consolidate spend and volume data from SAP. Provide critical data and support to site finance business-facing teams. Promote process standardization throughout the plant network, including Budgets, Forecast, LRP and Month End Reporting. Actively seek practices that will improve accounting processes and efficiencies. Ensure compliance with relevant governmental agencies, EHS and quality. Education and experience: Bachelor's degree in Accounting, Finance, or Business Administration. Four years of experience as a cost accountant in a multinational manufacturing environment. Direct SAP experience with general knowledge of support programs and third-party system applications. Expertise in cost accounting principles for manufacturing and corporate accounting practices and accounting theories required. Customer-focused able to provide outstanding service to the plant assigned Strong Excel, Word, and PowerPoint experience. Strong communication time management skills. 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

Lab 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. Challenging work with a global impact? We offer that. Competitive compensation and benefits? We offer that too. Welcome to AbbVie! At AbbVie Westport, we are now recruiting our newest Lab Analyst (Microbiology) to join our talented Microbiology Lab team on a 12-month fixed-term basis initially. As our new Micro Lab Analyst, you will perform routine microbiology laboratory activities, including environmental monitoring of cleanrooms, microbial analysis of site utilities and testing of raw material, commercial, clinical and development batches. You will have the opportunity to manage the microbial analysis of products and develop your career with an industry leader and all in the surrounds of Ireland's beautiful Westcoast. So if you are ready to join the AbbVie team in Westport, read on to find out more... In your new role, you will: Perform testing which may include environmental monitoring, water sampling, bioburden, endotoxin, growth promotion, in-process testing, Sterility testing, APET, Antibiotic Assay Complete all required report writing, including drafting and reviewing documentation, SOPs, protocols, training modules, investigations, reports, CAPAs and deviations. Perform trending of results and investigations into adverse or out of limit results Participate in the validation of equipment and microbiology test methods Support raw material, utility, in-process, release and stability testing of sterile products. Perform routine and non-routine Microbiological testing activities as required. Ensure that all testing is completed, reviewed and approved within agreed turnaround times. Ensure activities comply with product license commitments, cGMP, company quality standards, and legislative regarding health, safety, and environment. Qualifications Education and Experience 3rd Level Qualification in Microbiology or equivalent scientific degree 1-2 years experience in a similar role, preferably in Aseptic processing Working knowledge of both the Biopharma Industry and sterile processing Strong background in Aseptic and/or Microbiology preferred Excellent communicator, both verbal and written. Strong IT skills So, does this all sound like the right role for you? Then 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.

11 days agoFull-timeTemporary

Nchd, Psychiatry Department, Mental Health Services

HSEMayo

Post Specific Related Candidates must have at the latest date of application: Previous experience working in Psychiatry in the Irish Health Service at Senior House Officer/Registrar level is desirable. Full clean driving licence desirable Location Mayo Mental Health Services, Community Healthcare West, Co. Mayo Proposed Interview Date It is proposed to hold interviews as soon as possible after the closing date for CV submissions. HSE Area CHO 2 - Galway, Mayo and Roscommon Category Medical/Dental Informal Enquiries Dr. Orfhlaith McTigue - Consultant Psychiatrist - Tel: (094) 9042175 - Email: orfhlaith.mctigue@hse.ie Application Details Please send your CV to: E-mail: mcs.hrdept@hse.ie Contract Type Fixed Term Contract

5 days agoTemporary

EHS Engineer

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. Great salary and benefits? We offer that Ongoing learning and development? We offer that too Welcome to AbbVie! Our employees work every day to discover and address many of the world's most pressing health challenges. When you have patients depending on your solutions, you look for the best people to be part of the team. We are now inviting an EHS Engineer to join our team at AbbVie Westport, Co. Mayo on a 12-month fixed-term contract initially. As our new EHS Engineer, you will be responsible for creating a culture of strong safety engagement amongst employees and utilising the Operational Excellence framework to drive EHS improvements, compliance with EHS requirements, and the achievement of EHS KPIs. We have a diverse team here at AbbVie Westport and this role will give you the opportunity to work with a wide range of processes and products that make a real impact on patients on a global scale. So if you are ready to advance your career with AbbVie in Westport then read on and get your application started today! Key Responsibilities Actively engage with employees within the Business Unit (BU) to create an inclusive / ownership culture for Safety. Motivate, energise and influence the management teams to ensure fresh and leading-edge EHS programs, initiatives and activities are effectively implemented. Maintain EHS KPIs ensuring they are continuously up to date. Attend and chair safety meetings with key stakeholders to drive positive action and performance, ensuring appropriate timely action on KPIs showing a declining trend. Attend and support safety forums, provide direction for forums to ensure focus on key safety topics, provide safety information as relevant, and influence management and employees to ensure active engagement. Develop and deliver EHS Training modules in accordance with EHS Training Plan and risk assessment. Lead EHS Risk Assessment program and ensure all elements of facility, equipment, tasks, ergonomics and chemicals are appropriately risk assessed. Support our Supervisors/Managers to implement our EHS policy educating and encouraging them to drive the EHS programme. Support accident/incident investigation to ensure appropriate root cause analysis is completed and CAPAs implemented. Develop and support a system whereby Safety interventions/Good Observations are effectively recorded and managed. Promote and develop the Behavioural Safety Program, by active engagement and support of management and core teams. Coordinate EHS promotional activities to create a culture of engagement. Complete regular audits to ensure the business meets all EHS Regulatory and Corporate requirements and engage relevant team members on the GEMBA. Qualifications Education and Experience: Degree qualification in health & safety or degree in science/engineering with minimum diploma qualification in health & safety. Minimum 5 years EHS experience in a pharmaceutical or medical device environment. Experience in influencing others, including influencing upwards, to drive safety improvements. Experience in engaging employees to continuously improve the safety culture. Demonstrated knowledge of Irish health and safety regulations and industry best practices. Excellent teamwork, interpersonal, communication, organisation and decision-making skills. Good time management. Ability to handle multiple tasks simultaneously whilst maintaining close attention to detail. Thrives in a fast-paced work environment. Results-focused and committed. Demonstrated commitment to achieving high results in a demanding work environment If all this sounds like the right opportunity for you 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.

2 days agoFull-timeTemporary
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