Job Description Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what's possible and taking action. What You Will Achieve Working with Pfizer's dynamic engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment. As an Engineering Maintenance Technician, your knowledge and skills will contribute towards the goals and objectives of the team. Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Contribute to completion of projects, manage own time to meet agreed targets, develop plans for short-term work activities on own projects. Provide engineering support to develop scope of work, project execution plans, and associated engineering studies for equipment and component installation, modification etc. Provide necessary operational support as needed. Review preventive and corrective work order activities and provide equipment maintenance history review. Manage technical writing and document review. Ensure calibration compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices. Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans. Partner with Production and Quality Team Leads on troubleshooting and scheduling. Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture. Facilitate and participate in the investigation teams created to determine root cause of exemption reports, QARs and laboratory investigation reports. Serve as a liaison between quality, Operations and regulatory/Compliance to facilitate timely closure of investigations. Assist in the development the Preventative Maintenance program. Engage with site sustaining Engineering Operations for input and best practice. Work with Engineering teams in building the Maintenance Management database system (EAMS) Qualifications Must-Have Diploma/Degree in an Engineering/Technical Discipline or Electrical/Mechanical Trade Qualification 3+ years of experience Experience with Root Cause Failure Analysis PM/PdM optimization, and/or Failure Modes and Effects Analysis Strong knowledge and understanding of Current Good Manufacturing Practices {part of GxP} Excellent oral and written communication skills Experience with commissioning, qualification, start-up, and production support activities is desirable Experience executing Engineering tasks using Engineering Maintenance Management systems such as EAMS. Strong hands-on troubleshooting capability across mechanical and electrical systems. Ability to interpret electrical, mechanical, pneumatic, and logic diagrams. Experience with process automation systems, PLC diagnostics, and instrumentation is desirable. Good computer literacy and documentation skills. Working knowledge of MS Excel Nice-to-Have Bachelor's degree Relevant pharmaceutical experience What We Offer .. Why Choose Pfizer Competitive Salary and Shift Allowance* Multiple Permanent Positions Available Annual Bonus and Share Schemes Pension Scheme Long Term Income Protection Healthcare for You and Your Family Career Development Opportunities Subsidised Canteen Health and Wellbeing Initiatives On-site Gym and Saloon Sports and Social Club (Swim Society, Women's Mentoring Programme, Pfizer Pride & many more) Diverse and inclusive workplace It is a 4 cycle shift role for 24/7 Operation* Work Location Assignment:On Premise Additional Information In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position How to apply Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you! Purpose Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here! Engineering To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
A leading pharmaceutical company in Cork is looking for an experienced analyst to lead development and implementation of analytics for API processes. You will provide technical support for supply assurance projects, apply specialized skills to support chemical process development, and lead analytical method validation. Ideal candidates should possess a PhD or relevant degree with industry experience, and be proficient in various analytical techniques. The position requires strong problem-solving abilities and excellent communication skills. #J-18808-Ljbffr
Job Summary Development and implementation of analytics for new API processes and technology in manufacturing sites. Provide technical support and leadership for supply assurance projects. Job Responsibilities Apply highly specialized analytical skills to support chemical process development, pilot plant demonstrations, and full-scale qualification batches as part of the Development team. Develop, evaluate and verify analytical methods across a range of techniques as required to support projects. Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team. Contribute a range of highly innovative analytical ideas to support global process development projects. Demonstrate problem solving delivering process and analytical understanding. Provide analytical support in technical transfer of analytical methods to manufacturing sites. Co‑ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands. Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups. Investigate new technologies and analytical approaches. Complete reports, memos and lab notebook experiments to a high standard and meeting required deadlines. Contribute to the analytical team program of continuous improvement. Ensure the ongoing safe and efficient operation of facilities. Qualifications/Skills Extensive knowledge and experience of analytical principles and procedures. Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC‑MS/MS, GC‑MS, KF. A strong background in impurity isolation and identification using LC‑MS to support the development and troubleshooting of chemical processes is desirable. Experience in HPLC/UPLC method development. GC method development experience is desirable. Experience in pGTI method development and quantification is desirable. Experience of method validation and method transfers, including generation and review of MT and validation protocols and reports is desirable. A proven ability to plan and work independently. Must work under consultative direction toward predetermined long‑range goals; project management experience a plus. Ability to determine and pursue courses of action necessary to obtain desired results; develops advanced ideas and guides their development into a final product. Demonstrated application of Six‑sigma tools and practices with a focus on continuous improvement for work processes. Excellent interpersonal skills and ability to work in a collaborative, team‑driven environment. Excellent written and verbal communication skills. For Research Analyst: a PhD in analytical chemistry ideally combined with 0+ years' experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and up to 2+ years' experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role. Work Location Assignment: On Premise Additional Information In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position. Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. #J-18808-Ljbffr
Job Summary Development and implementation of analytics for new API processes and technology in manufacturing sites. Provide technical support and leadership for supply assurance projects Job Responsibilities Apply highly specialised analytical skills to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the Development team. Develop, evaluate & verify analytical methods across a range of techniques as required to support projects. Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team. Contribute a range of highly innovative analytical ideas to support global process development projects. Demonstrate problem solving delivering process and analytical understanding. Provide analytical support in technical transfer of analytical methods to manufacturing sites Co-ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands. Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups. Investigate new technologies and analytical approaches Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines. Contribute to the analytical team program of continuous improvement. Ensure the ongoing safe and efficient operation of facilities. Qualifications/Skills Extensive knowledge and experience of analytical principles and procedures. Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC-MS/MS, GC-MS, KF. A strong background in impurity isolation and identification using LC-MS to support the development and troubleshooting of chemical processes is desirable. Experience in HPLC/UPLC method development. GC method development experience is desirable. Experience in pGTI method development and quantification is desirable. Experience of method validation and method transfers, including the generation and review of MT and validation protocols and reports is desirable. A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project. Project management experience a plus here. The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results. Develops advanced ideas and guides their development into a final product. Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes. Excellent interpersonal skills and the ability to work in a collaborative, team driven environment. Excellent written and verbal communication skills. For Research Analyst, a PhD in analytical chemistry ideally combined with 0+ years' experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and ideally up to 2+ years' experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role. Work Location Assignment:On Premise Additional Information In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position How to apply Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you! Purpose Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here! Research and Development To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.
