Company description: Use Your Power for Purpose Every day, Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. What You Will Achieve In this role, you will: Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications. Conduct rigorous sampling and statistical process control procedures to identify deviations from standards. Approve investigations and change control activities to maintain compliance with configuration management policies. Contribute to moderately complex projects, managing time effectively and developing short-term work plans. Independently assess Change Control activities for potential Quality and Operational Good Manufacturing Practices (cGMP) impacts. Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed. Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards. Job description: Here Is What You Need (Minimum Requirements) High school diploma (or equivalent) with 8+ years of experience or associates degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards Strong critical thinking skills Ability to work effectively within own team and interdepartmental teams Good working knowledge of Microsoft Excel and Word Proactive approach to problem-solving Required profile: Bonus Points If You Have (Preferred Requirements) Experience in quality administered systems Strong organizational skills and attention to detail Experience with regulatory compliance and documentation Ability to mentor and review the work of other colleagues 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! What we offer: 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! Skills: QA specialist QA Operations Specialist Operations
Company description: Use Your Power for Purpose At Pfizer, our purpose is to deliver breakthroughs that change patients lives. Your contributions will directly impact the development of new therapies and vaccines, ultimately improving the lives of patients around the world. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally. About Pfizer Process Development Centre The Pfizer global Process Development Centre (PDC) is an innovative team which develops new API processes and technology for the Pfizer global manufacturing network. Additionally, the PDC leads and supports various supply assurance projects for the global manufacturing network. Our team works closely with global research and operations teams enabling the manufacture of life saving medicines. About the role We now have an exciting opportunity for a Research Chemist to join our team based in Cork, Ireland. The successful candidate will work as part of a multi-disciplinary team working with leading edge technology. The PDC is a vibrant, dynamic team with excellent career development and advancement opportunities. This role will require attendance at our facility in Cork. Specific Purpose Contract The purpose of this specific purpose contract is contingent upon project support requirements in PDC for the External Supply OpU Polaris initiative, which include but are not limited to the following focus areas: i) Process and Analytical development laboratory activities to support optimisation of the Isavuconazole API process and ii) Process and Analytical development laboratory activities to support the optimisation of other priority API processes identified for optimisation within the External Supply portfolio as deemed appropriate. Job description: What we offer An attractive and competitive package of pay and conditions. Excellent opportunities for career enhancement and development. A well-established further education programme. Opportunity to travel to other Pfizer sites and locations. A strong personal development programme. About the position Reporting to the Senior Process Development Manager, the successful candidates key responsibilities, commensurate with the position are: Apply synthetic chemistry and mechanistic expertise to support commercial API processes at relevant API sites. Apply highly specialised synthetic chemistry theoretical and process development skills to design and maintain safe, efficient, and robust processes including full-scale qualification and/or commercial validation batches meeting contemporary regulatory standards. Contribute a range of highly innovative chemistry and process development ideas to support global process development projects. Demonstrate problem solving delivering chemistry and process understanding. Investigate new technologies and process development approaches to bring added value to Pfizer Global Supply. Complete reports, memos and eLN experiments to a high standard and meeting required deadlines. Contribute to the PDC chemistry team program of continuous improvement. Ensure the ongoing safe and efficient operation of PDC facilities. Required profile: The ideal candidate will possess: A minimum of a PhD in synthetic chemistry. Experience in the pharmaceutical industry within a process development role is desirable but not required. Extensive knowledge and experience of synthetic chemistry and reaction mechanisms including the ability to apply knowledge to solve problems. Knowledge of contemporary quality and regulatory guidance pertaining to the control of impurities, including potentially genotoxic impurities is desirable. Knowledge of process development and scale-up principles, process validation and technical transfers. Excellent practical synthetic laboratory experience and skills across a broad range of chemistries. Background in impurity isolation and identification to support the development and troubleshooting of chemical processes. A proven ability to plan and work independently. 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. Excellent written and verbal communication skills. Positive interpersonal skills and the ability to work in a dynamic, matrix team driven environment. 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 What we offer: 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! Skills: Research Chemist Chemist Research
Company description: Use Your Power for Purpose At Pfizer, our purpose is to deliver breakthroughs that change patients lives. Your contributions will directly impact the development of new therapies and vaccines, ultimately improving the lives of patients around the world. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally. About Pfizer Process Development Centre The Pfizer global Process Development Centre (PDC) is an innovative team which develops new API processes and technology for the Pfizer global manufacturing network. Additionally, the PDC leads and supports various supply assurance projects for the global manufacturing network. Our team works closely with global research and operations teams enabling the manufacture of life saving medicines. About the role We now have an exciting opportunity for a Research Analyst to join our team based in Cork, Ireland. The successful candidate will work as part of a multi-disciplinary team working with leading edge technology. The PDC is a vibrant, dynamic team with excellent career development and advancement opportunities. This role will require attendance at our facility in Cork. Specific Purpose Contract The purpose of this specific purpose contract is contingent upon project support requirements in PDC for the External Supply OpU Polaris initiative, which include but are not limited to the following focus areas: i) Process and Analytical development laboratory activities to support optimisation of the Isavuconazole API process and ii) Process and Analytical development laboratory activities to support the optimisation of other priority API processes identified for optimisation within the External Supply portfolio as deemed appropriate. Job description: 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. Required profile: Requirements for all Global Job Levels 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. 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. 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. What we offer: Work Location Assignment: On Premise 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! Skills: analyst Research Research Analyst
Company description: 2026 Graduate Programme, Pfizer Ringaskiddy, Cork Pfizer Ringaskiddy Cork are delighted to be accepting applications for our Graduate Programme commencing in September 2026 where we offer you the chance to complete a 23month programme. At Pfizer Ringaskiddy we are passionate about building a diverse work environment where all colleagues feel respected in their uniqueness. We are proud of our ongoing efforts to foster diversity & inclusion to ensure all colleagues have the freedom to be who they are and to bring their whole self to work. Together, we continue to build a culture that encourages, supports, and empowers our people. The award-winning Pfizer Ringaskiddy, Cork site is seeking candidates for the 2026 graduate programme, currently in its 21st year. Our site plays a critically strategic role within Pfizer, it is the global site for new small molecule API products through scale up and launch, as well as manufacture of large volume patented and off-patent medicines. Colleagues on the site use state of the art equipment and leading-edge technology, as well as work collaboratively with Research and Development to provide the highest quality innovative products to the market. Job description: About the Graduate Programme This is an amazing opportunity to progress your career with one of the largest and most successful bio pharma organisations in the world. A significant number of graduates who have previously completed the graduate programme at the Pfizer Ringaskiddy site have gone on to have very successful careers in Pfizer both at local site and global levels. The site has a strong coaching culture, and a structured mentoring programme is provided. Full training will be provided by a comprehensive induction programme. During the programme, participants will be involved in the following: One-year induction programme. Structured mentoring & coaching objective setting during each assignment. Attend management training programmes. CPD 6 module professional training programme. Personal effectiveness and leadership development training. Attend and present at Senior Executive meetings e.g., communications meetings, cross site teams, leadership team meetings. Support cost improvement projects for key API manufacture processes. Be responsible for the management of various day to day operations as well as being assigned to be a coleader of specific projects. This is a fantastic training & development opportunity for a committed graduate. Required profile: Requirements: Be completing or just completed an Honours Degree (or equivalent/higher) in one of the following related courses. Chemical, Electrical, Mechanical Engineering or Environmental Chemistry/Industrial Chemistry Pharmacy/Regulatory Affairs or similar Available to start in September 2026 What We Offer? We have several positions in both our Operations and Innovation & Launch Sciences Teams. 23-month contract with Competitive Salary plus Bonus Schemes, Healthcare, Pension, Share Scheme, Long Term Income Protection and Life Assurance. An on-site role based on our vibrant Ringaskiddy API Campus with the opportunity for flexible working arrangements. Free parking or you can sign up to our shuttle bus service between Campus and Cork City. Ringaskiddy is close to Cork City and offers onsite gym, health & wellness programs, employee development programs, subsidized canteen and many more benefits for you to enjoy! Initial accommodation finding support. 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 What we offer: 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! Skills: Graduate Programme Pfizer Graduate programme
Job description: The technical services team are seeking an experienced process scientist whose role will focus on supporting commercial manufacturing and technology transfers to the drug substance small and/or large-scale manufacturing facility. This role will be located at the Pfizer Grange Castle site. The drug substance facility is a multiproduct manufacturing area specialising in the manufacture of therapeutic proteins derived from mammalian cell culture for a range of clinical and commercial products. This position will report to the drug substance technical services lead and will be an integral part of a high performing technical services team whose role will involve: Support commercial manufacturing to meet commercial requirements including investigations, process robustness and process improvements. Scale up of mammalian cell culture processes from bench and pilot scale to a pilot & large-scale manufacturing facility. Perform, present and execute facility fits, mass balance generation, equipment sizing, gap assessments and mitigation of operational challenges foreseen to ensure an equivalent process is transferred to Grange Castle Provide independent decision making for strategic input into facility and equipment design Prepare, review & execute technology transfer protocols, supporting documentation, design of experiments and at scale process trials to deliver an efficient technology transfer Author and review responsible sections of regulatory dossiers including health authority query responses Partners with the management and technical team to identify best practices, technical transfer efficiencies and optimisations during technical transfer. Develops and maintains effective working relationships with other division groups supporting technology transfer, validation and process support. Required profile: Minimum of 3 - 6 years of mammalian cell culture process development/ late-stage characterisation and technical transfer / technical services experience in stainless steel and/or single use facilities Demonstrated history and in-depth knowledge of cell culture scale up practices, technical transfer, facility fit, equipment sizing and mass balance generation for clinical/ commercial manufacture Knowledge and experience of process validation strategies, studies and requirements Knowledge of regulatory submissions and response of queries from health authorities In depth knowledge of cGMP regulatory requirements related to the design and control of drug substance processes Skills: High technical capability, interpret complex data, problem solving and technical learning. Promote information sharing and excellent interpersonal skills Capability of working in a multi-disciplinary team environment to tight timelines Effective communication, planning and organisation skills to deliver documentation. Work Location Assignment: Hybrid 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 Skills: mammalian cell cell culture scientist
Job description: In this role, you will: Engage in activities across multiple cross-functional areas, including production planning, total quality management, systems, manufacturing, equipment and facilities engineering, material management, and process engineering. Utilize innovative communication tools and techniques to resolve complex issues between teams, foster consensus, and support continuous improvement opportunities and projects. Perform lab qualification work, provide technical justification for new raw materials, and offer Subject Matter Expert support during major investigations. Troubleshoot and provide sustainable solutions for root-cause processing and safety problems, support plant process changeovers and clean ups, and ensure alignment between processes, plant, automation, and operators. Adhere to current Good Manufacturing Practices (cGMP), manage product knowledge during tech transfer and manufacturing campaigns, and foster a culture of Right-First Time through partnerships with Operations and the use of Operational Excellence (OE) principles. Required profile: Relevant Chemistry or Bachelors degree with 3+ years experience or have a PhD in organic chemistry or related field (or equivalent synthetic chemistry experience). Demonstrated ability to provide technical solutions for complex problems through extensive product and process knowledge. Good understanding of process manufacturing and computer systems. Ability to lead change and exhibit strong collaborative skills. Excellent mentoring and interpersonal skills. Strong analytical and problem-solving skills. Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical industry experience. Experience with continuous improvement methodologies such as Lean or Six Sigma. Familiarity with regulatory requirements and cGMP. Strong project management skills. Experience with process optimization and troubleshooting. Strong organizational skills and attention to detail. Ability to adapt to changing priorities and work in a fast-paced environment. Excellent written and verbal communication skills. Nice to Have Relevant Pharmaceutical industry experience. Awareness of relevant ICH guidelines and API regulatory requirements. API process validation experience/knowledge. Skills: chemistry computer systems chemist
Company description: At Pfizer, technology impacts everything we do. Our digital and data first strategy focuses on implementing impactful and innovative technology solutions across all functions from research to manufacturing. Whether you are digitizing drug discovery and development, identifying solutions, or making our work easier and faster, you will be making a difference to countless lives. Pfizer's Global Business Services (GBS) Transformation and Project Management (T&PM) Office is responsible for driving enterprise-wide transformation that delivers measurable business value through strategic project execution, operational excellence, and data-driven decision-making. This Analyst role within the Metrics & Measurement team focuses on delivering impactful automations and analytical solutions that support strategic decision-making and business process efficiency. The ideal candidate will have hands-on experience developing and deploying automation solutions using Microsoft Power Apps and Power Automate, along with strong skills in data visualization and reporting. This role requires close collaboration with cross-functional teams and the Digital organization to ensure timely, high-quality delivery of automation and analytical tools that support GBS transformation goals. Job description: Deliver automations and analytics solutions that support strategic decision-making and improve cross-functional alignment. Collaborate with key stakeholders and Pfizer Digital to ensure timely and high-quality delivery of automation and analytical tools. Develop and maintain dashboards, ensuring data accuracy, periodic refreshes, and actionable insights. Monitor and report on project progress against key performance indicators, including financials, timelines, risks, and scope variances. Support the integration of Pfizers technology platforms (e.g., SAP ERP, BI-BOBJ systems) into analytics and automation workflows. Contribute to the continuous improvement of GBS processes through data-driven insights and automation. Required profile: 13 years of hands-on experience in Power Apps and Power Automate development, with a strong understanding of automation design and deployment. Basic SQL or data modeling skills. Experience or familiarity with UX design principles is a plus, especially in building intuitive and user-friendly automation interfaces. Proficiency in Microsoft Excel and data visualization tools (e.g., Power BI); experience with SAP ERP and BI systems is a plus. Strong organizational and problem-solving skills, with the ability to manage multiple priorities and deliver high-quality results under tight deadlines. Effective communication skills, written and verbal, for presenting insights and collaborating across teams and stakeholders. Comfortable working in a matrix, cross-functional environment. Power Platform Certification or equivalent is a plus. What we offer: Skills: analytics automation data
Company description: Pfizer Ireland Pharmaceuticals' Grange Castle manufacturing plant is situated on a 90-acre site in South Dublin. The state-of-the-art technology and production expertise at Grange Castle result in the production of quality-driven products that improve people's lives around the world. The site houses advanced pilot plants, laboratories, and equipment for developing processes for producing various biological drugs, including proteins. The experienced Automation Engineer will be part of the Grange Castle NPI (New Product Introduction) project team, working in our highly automated plant at Grange Castle. Reporting to the Automation Lead, this role is part of the core Engineering Team, delivering on key projects as required. Job description: Working as part of an experienced Automation NPI site Project Team. Collaborating with Process SMEs, CQV Leads, and Automation Engineers to understand process requirements. Generating all the key technical inputs into functional design specifications from all stakeholders. Participating in and signing off on key Functional design aspects as required. Implementing the ACPs (Automation Change Pack) to make the required code changes. Supporting project reviews internally with key stakeholders within Automation and customers as required. Required profile: Degree in Electrical/Electronic or Chemical Engineering, or a related field with substantial experience. Over 5 years of experience as an Automation Engineer within the biotechnology industry in a regulated GMP environment, delivering Emerson DeltaV solutions (S88 model) and/or high-level expertise in PLC and SCADA based systems including integration. Ability to liaise with process engineers to define scope and deliver on specifications with very strong documentation skills and attention to detail. Automation Compliance lifecycle & Change management relevant experience Experience with process plant commissioning. Strong team player with the ability to develop relationships and work closely with several cross-functional disciplines, both within and outside of the function and organization. Good working knowledge of ISA95 and ISA88, CFR (Code of Federal Regulation) Part 11, EU (European Union) Annex 11. Excellent communication skills with the ability to formulate thoughts in a clear and concise manner to provide clarity and a path forward on any issues. Skills: automation NPI Projects engineer
Company description: The Pfizer global Process Development Centre (PDC) is an innovative team which develops new API processes and technology for the Pfizer global manufacturing network. Additionally, the PDC leads and supports various supply assurance projects for the global manufacturing network. Our team works closely with global research and operations teams enabling the manufacture of life saving medicines. Job description: Reporting to the Senior Process Development Manager, the successful candidates key responsibilities, commensurate with the position are: Apply synthetic chemistry and mechanistic expertise to support commercial API processes at relevant API sites. Apply highly specialised synthetic chemistry theoretical and process development skills to design and maintain safe, efficient, and robust processes including full-scale qualification and/or commercial validation batches meeting contemporary regulatory standards. Contribute a range of highly innovative chemistry and process development ideas to support global process development projects. Demonstrate problem solving delivering chemistry and process understanding. Investigate new technologies and process development approaches to bring added value to Pfizer Global Supply. Complete reports, memos and eLN experiments to a high standard and meeting required deadlines. Contribute to the PDC chemistry team program of continuous improvement. Ensure the ongoing safe and efficient operation of PDC facilities. Required profile: A minimum of a PhD in synthetic chemistry. Experience in the pharmaceutical industry within a process development role is desirable but not required. Extensive knowledge and experience of synthetic chemistry and reaction mechanisms including the ability to apply knowledge to solve problems. Knowledge of contemporary quality and regulatory guidance pertaining to the control of impurities, including potentially genotoxic impurities is desirable. Knowledge of process development and scale-up principles, process validation and technical transfers. Excellent practical synthetic laboratory experience and skills across a broad range of chemistries. Background in impurity isolation and identification to support the development and troubleshooting of chemical processes. A proven ability to plan and work independently. 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. Excellent written and verbal communication skills. Positive interpersonal skills and the ability to work in a dynamic, matrix team driven environment. What we offer: An attractive and competitive package of pay and conditions. Excellent opportunities for career enhancement and development. A well-establishedfurther education programme. Opportunity to travel to other Pfizer sites and locations. A strong personal development programme. Skills: medicine chemist synthetic chemistry
