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Office Administration Assistant

McSharry Foley Ltd t/a whoops.ieSligo

Whoops.ie are busy and growing Insurance Brokers based in Stephen Street, Sligo for over 30 years. We are currently recruiting an Office Administration Assistant for our team. This is an office-based role, with no weekend work. The ideal candidate will have: Full training will be provided along with opportunities for career progression and an industry qualification. Unqualified applicants must be willing to study alongside work to obtain their insurance qualifications.

22 days agoFull-time

Sales Executives / London Based / Immediate Start

The Directory GuysOutside of Ireland

Due to continuing expansion, TDG is looking to recruit a number of experienced Sales Executives for our location in Uxbridge, West London. This role involves developing new client relationships and opening doors for new business development. Fantastic career progression, with the potential to work and travel overseas to any of our other 3 offices (Canada, Australia, New Zealand) The company is the market leader in their sector, renowned for their innovative nature. The company boasts an impressive product portfolio allowing a creative salesperson to flourish. What you will need: • Previous experience working in a sales/telesales/account management environment is essential • Strong communication skills • Experience working towards monthly targets • Ability to cross-sell and upsell • Strong ability to overcome objections • You. must be a great problem solver • Excellent communication skills - written and verbal • Ability to manage your own workload • Strong customer focus On Offer: • Salary is negotiable based on experience level + Bonus and commission • Opportunities for travel and work abroad • Defined targets for career progression • Constant training and development • Sales and Team Leader roles available To apply click APPLY NOW to submit your CV.

10 days agoFull-time

Basic Grade Physiotherapist

North West Therapy CentreSligo

The Multiple Sclerosis North West Therapy Centre (MS Centre) Ballytivnan, Sligo Invites applications for the post of 1 X Basic Grade Physiotherapist (full-time) Dual role position required to work in Sligo University Hospital/MS Centre (Fixed term contract until 31st December 2022) 1 X Basic Grade Physiotherapist Post (30 hours per week) Role-based at the MS Centre (Fixed term contract initially until 31st December 2022, contract may be extended) Job Descriptions are available from Front Office Manager: 071 91 44748. Please send a CV with a cover letter to the MS Centre Manager by Friday 28th January 2022 via post or Click Apply Now to upload your CV and cover note. NB: Please ensure to specify your interest in 30/35 hour contract or both in the subject line of your covering letter. The MS NW Therapy Centre is an Equal Opportunities Employer. A company limited by guarantee

2 hours agoFull-time

Music Teachers

Creative KeyboardsNationwide€35 per hour

Creative Keyboards are now hiring! Teachers wanted to teach beginner keyboard as an after-school activity in the following counties: Dublin / Wexford / Kildare / Cork / Galway / Carlow This role would suit a student or parent returning to work with music experience up to Grade 4 in Piano. Requirements: Salary:  €35 per hour. Additional Info:  Lesson plans provided. Hours of work:  from 1 pm 3/5 afternoons per week for 2/3 hours. Click  Apply Now  to submit your application today!

3 days agoPart-time

Women Managing Business: Female Leadership Program

Optimum Results LtdNationwide

Women Managing Business: Female Leadership Program Free Webinar this Thursday 27th: Click Here To Sign Up To Our Free Webinar Do you need help in formulating a plan to  achieve career progression  in your current organisation or industry? Are you excited by the prospect of senior management roles but  fearful of the increased responsibility ? Do you want to  become a more confident communicator  at work and learn the art of self-promotion? Do you want to gain the confidence and skills to  excel at the same level as your male peers ? A Program Inspired by the Gender-Related Challenges to Career Progression Experienced by Women Every Day at Work. The identification by research experts of distinctive barriers faced by women in the workplace has inspired the development of The Optimum Results Women Managing Business series of courses.  We continue to see talented women drop out of industry prematurely, losing the confidence and ambition to progress their careers.  The  Women Managing Business  series has been designed by women with first-hand experience of these gender-specific barriers experienced by female corporate executives. Click Here To Visit Our Website For More Information

2 days agoRemote

Technical Shift Lead

AbbvieBallytivnan, Sligo

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 lead a high performing team? We OFFER that. Be part of a Great Place to Work? 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 Technical Shift Lead (Biologics) to be part of our extended leadership team in our Ballytivnan site in Sligo. Reporting directly to the Operations Lead, you will be lead, and coach your team and be responsible for producing biologics fill finish materials as per organizational needs in line with all relevant safety and quality compliance requirements. Day to day in this role, you will: Lead, coach and mentor your team Be responsible for the supervision and execution of filling, lyophilization, equipment preparation, formulation, buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives. Promote a culture of contamination control and compliance with aseptic best practice. Liaise with functional leadership teams (Ops, Quality, Engineering, Supply Chain etc) on operational activities Daily reporting on the status of all operations and support activities. Provide clear and concise communication to your team on their tasks and goals so that they can work effectively. Provide technical expertise for investigation and resolution of process deviations, root cause investigation, CAPAs, process improvements, review and approval of change controls Responsible for verification and update of manufacturing control system transactions accurately and in a timely fashion. Act as key point of technical contact for aseptic fill finish activities. Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing. Responsible for driving operations excellences and Key operations targets including OEE where applicable. Provide direct interface as a subject matter expert with QA department to interaction with HPRA, FDA and applicable health authority and internal audits. Lead cross functional risk assessments and continuous improvement projects Ensure the execution of fill finish, lyophilization, equipment preparation, buffer preparation and formulation processing activities to meet clearly stated operating objectives. Responsible for manufacturing compliance with all safety, environmental and quality related SOPs. Drive safety improvements and initiatives across the operation Promote a culture of Right First Time, Behavioural Based Safety, Always Audit Ready and Human Error Reduction within their team. Work closely with the other Technical Shift Leaders to ensure interdepartmental activities are planned and executed safely. Qualifications Does this sound like the right role for you? so read on for the education and experience requirements.... You will have a Degree, Masters or PhD in Life Sciences, Process Engineering, Biopharmaceutical Engineering or Chemical Engineering discipline With 5 + years experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry and 1+ years team leadership experience 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) Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality and safety requirements. Still interested? 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

Biologics Technician

AbbvieIreland; Ballytivnan, Sligo

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. Ready to invest in your career? We offer that Recognition for your commitment & hard work? We offer that too Welcome to AbbVie! At AbbVie, our strength lies in our team of experts who conduct ground breaking science on a global scale every day. At our site in Ballytivnan, we are expanding our facility into a multi-million dollar state of the art biologics plant that will bring ground breaking scientific research to real life solutions for our patients. We are currently sourcing Biologics Technicans to join our operations team that is responsible for the manufacture of our biologics products in a safe, quality focused enviroment. Here is a snapshot of your day to day responsibilities: Daily production operations operating different equipment while documenting all activities in line with cGMP requirements. Efficiently operating all biologics processes minimizing material loss - Fill Line, Autoclave, Equipment Washer, Headspace Analyzer, Bioreactors, Chromatography Columns, Filtration Systems, Equipment Cleaning and Sterilization, Equipment Pressure Tests, Equipment/Filters Integrity Tests, Water Baths, Isolators and Lyophiliser, Headspace Analyser, as applicable. Perform final product visual inspection and perform product intermediary packaging, as applicable. Assemble and inspect equipment in the manufacturing area to confirm its operational status. Perform all in process testing methods and monitor Process Alarms. Material receipt from warehouse, verifying all pertinent documentation and transfer of final material to warehouse inventory. Diagnose and resolve events or exceptions of production equipment and processes. Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations following the procedures and policies of the plant, division, and the corporation. Active Participation in Factory Acceptance testing, Site Acceptance Testing and commissioning and qualification of equipment. Adhering to all relevant policies relating to Quality & Safety. Ensure successful external inspections, and Division and Corporate audits. Active participant in the development of batch records and electronic batch records for the site. Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures. Qualifications So what education & experience do you need? You will have Irish Leaving Certificate or equivalent with manufacturing experience (3rd level qualification is preferred) 1 year in Batch processing operations in an FDA/ HPRA regulated industry is highly desirable A good knowledge of cGMP and regulatory requirements relating to the biologics/pharmaceutical industry is desirable. Experience of operating in a highly automated environment and safe handling of dangerous chemicals is highly desirable. Good I.T. skills are required Possessing aseptic techniques and sterile fill experience is a distinct advantage for operators assigned to Fill Finish Requires proven problem solving skills and ability to troubleshoot So does this sound like the right next career move for you? then come and join AbbVie! 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

EHS Manager

AbbvieSligo

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. A Total Rewards package that recognises your value? We offer that Investment in your 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 recruiting a EHS Manager to be part of our leadership team in our Manorhamilton Road site in Sligo. Reporting directly to the Engineering Manager, the EHS Manager is responsible the overall direction of the EHS group onsite. They will manage site safety and environmental activities in line with all relevant corporate and regulatory agency requirements. Are you intrigued? Do you want to learn more? A snapshot of your key responsibilities as EHS Manager would be: Ensure that the necessary systems and procedures are available and operational to evaluate and control all aspects of EHS. This includes the following: Ensure safety standards are achieved and safe working practices are followed at all times. Management and leadership of site EHS activities ensuring compliance with all safety & environmental requirements. Management of EHS policies and procedures to ensure that all site-based activities are completed to corporate safety guidelines and standards & to ensure that safe working practices are followed at all times. Management and leadership of site EHS activities ensuring compliance ensuring compliance with Industrial Emissions license conditions and that routine reporting is conducted with relevant regulatory agencies. Compliance to ISO 14001 and OHSAS 18001 and Corporate Management and Technical Standards. Lead site safety and environmental activities through EHS Engineer and Environmental Specialist personnel to deliver programs, policies and procedures that ensure site compliance with all EHS requirements. Qualifications So, what do you need to do this role? Education & Experience: A minimum of a Diploma or Degree in EHS, Science or related discipline. Masters would be an advantage. This information is confidential to AbbVie. The user is responsible for using the appropriate version of this document. 7-10 years plus of Background in engineering/manufacturing, with relevant managerial experience. 3-5 years plus of Detailed knowledge of cGMP and regulatory requirements relating to the regulated healthcare industry. 5 years plus of Demonstrated project management skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements. 2 years plus of direct people management experience at management level. Total combined minimum years of experience required 7 – 10. So, are you ready to join our team? 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

Validation Manager

AbbvieSligo

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. Ready to lead a high performing team? We offer that Want to invest in your career 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 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 currently recruiting a Validation Manager (Leader) to be part of our extended leadership team in our Ballytivnan site in Sligo. Reporting directly to the Quality Director, you will lead a high performing team that is responsible for the development and maintenance of the biologics validation program and ensure AbbVie and external regulatory, quality, and compliance requirements are met. Does this role entice you? Then read on for some of the day-to-day responsibilities: • Develop, coach and mentor your team to perform to their highest capabilities • Coordination / direction and active participation in the validation and qualification of equipment, utilities, processes and software in compliance with AbbVie policies, FDA, European cGMP and GAMP standards. • Generation/maintenance/execution of Project Validation Plans and schedules • Generation of validation protocols and final reports to cGMP standards. • QA support for validation investigations and implementation of corrective actions. • Creation/Review/Approval of various validation and qualification documents • Management of validation, exception event, and change control processes. • Documenting all activities in line with cGMP requirements. • Performing cross training within the team and training of new team members. • Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems. • Coordinating activities to maximize the effectiveness of all of the team members. • Communicating with peers and management regarding activities in the area, including elevation of events or concerns. Qualifications So, what education & experience do you need for this role? You will have • A relevant degree in engineering or scientific discipline with 3 years plus validation/Quality experience in sterile/aseptic environment especially in the commissioning and qualification area • 3 years plus of knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry • Demonstrated leadership capabilities to build and coach a diverse team • Ability to partner and provide technical expertise to wider leadership team and cross functional teams 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

Validation Engineer

AbbvieSligo

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. Want to be part of a Great Place to Work in Ireland? We offer that too. We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work. We are recruiting for a Validation Engineer to join our team at our Manorhamilton Road site in Sligo. Reporting directly to the Validation Team Lead, you will be responsible for coordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements. Are you intrigued? Do you want to learn more? A snapshot of your key responsibilities as Validation Engineer would be: Ensure all computerised systems are qualified in compliance with Data Integrity policies and regulatory requirements. Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards. Generation/maintenance of the Validation Master Plans. Generation of validation plans, protocols and final reports to cGMP standard. Review / approval of all protocols and final reports. Management of validation change control process. Adheres to and supports all EHS & E standards, procedures and policies Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines. Close contact with internal and external auditors, e.g. FDA, HPRA. Qualifications Education and Experience; 3rd level qualification in a relevant engineering or scientific discipline. A minimum of 2 years’ experience in a cGMP regulated environment. A good understanding of regulatory requirements. 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
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