SK pharmteco, part of SK Inc, is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art small molecule manufacturing facilities in Korea, US, and Ireland. The SK Small Molecule Europe facility located in Swords, Co Dublin, Ireland has led the way in the development, scale-up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we make some of the world’s most important medicines. Further information on SK pharmteco can be found at www.skpharmteco.com Current Need A vacancy now exists for a PhD Chemist within the R&D group. This position is based at the R&D Centre in Swords, Co Dublin. The R&D Centre has co-located technical and operational expertise, including analytical expertise that supports the development and manufacture of clinical and commercial products (small molecule APIs). The R&D Chemist will have experience in synthetic organic chemistry. They will be responsible for providing support for all aspects of new and existing chemical processes development, technology transfer, process scale-up, process safety, process monitoring, and process troubleshooting for small molecules. The role will involve cross functional collaboration with other functions including Operations, Quality, EHS and external stakeholders working towards existing and new product introduction and ensuring all processes are understood, robust, efficient and in control. Essential Responsibilities Lead development projects in the laboratory, including route scouting and route development, proof of concept, crystallisation optimisation, and process safety assessment. Provide technical support to the manufacture of APIs and intermediates manufactured at SK pharmteco with a focus on optimisation and investigation support. Identify and implement projects to optimise processes, considering scale-up and manufacturing aspects and Critical to Quality Attributes. Leverage data monitoring and PAT tools in the laboratory such as FBRM, Raman, IR, as required. Identify and implement new technologies to support development for the business needs of the site. Coordinate tech transfer activities for introduction of new clinical and commercial products to the site, including process development in the laboratory, customer engagement, troubleshooting, documentation, and campaign readiness. Support chemistry assessments for new products as required. Lead optimisation projects on throughput and yield in collaboration with Operations engineers. Support continuous process verification through collection and trending of data for commercial products, identifying Out of Trends (OOT) and Statistical Alert Events (SAE) and leading investigations where required with support from R&D engineers and analytical chemists. Actively participate in manufacturing campaign performance support teams. Lead and support quality and safety investigations. Collaborate with R&D analytical chemists and Operations engineers on new products introduction and scale up activities Minimum Requirements Strong technical background in chemistry. PhD in organic chemistry. 3+ years of experience in the pharmaceutical industry Strong interpersonal and communicational skills and demonstrated ability to work across a matrix. Excellent problem solving skills and commitment to continuous improvement. Experience in project management, troubleshooting and continuous process verification. Demonstrated capability in the use of standard tools for root cause analysis and standard statistical tools. Demonstrated capability in the use of various analytical/diagnostic tools including PAT, chromatography and process safety. Ensure that GMP, Quality, Health & Safety are considered in all aspects of the role. Other Benefits include: An excellent opportunity for career enhancement & development. Competitive base salary. Annual bonus linked to business results. A well-established further education program. Pension scheme. Private healthcare. SK pharmteco SM Europe is an equal opportunity employer #J-18808-Ljbffr
AR&D Analytical Chemist 12 month contract Location: Swords Campus SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver life‑changing therapies that improve patient outcomes and save lives’. The SK pharmteco Small Molecule, Europe, facility located in Swords, Co Dublin, Ireland has led the way in the development, scale‑up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we have made some of the world’s most important medicines and continue to do so. Further information on SK pharmteco can be found at skpharmteco.supremeclients.com Current Need Cpl in partnership with the SK pharmteco Small Molecule, Europe, facility located in Swords, are looking for an AR&D Analytical Chemist experienced in analytical method development onsite for a 12 month contract. This position is based at the R&D Centre in Swords, Co Dublin. The R&D Centre has co‑located technical and operational expertise, including analytical expertise that supports the development and manufacture of clinical and commercial products (small molecule APIs). Position Description The Analytical Chemist will be responsible for providing technical support for all aspects of analytical methodology, method development, transfer, qualification and troubleshooting pertaining to the manufacture of small molecule APIs and intermediates. The successful candidate will also provide support in the day‑to‑day running and maintenance of the AR&D laboratories, including equipment. The successful candidate will collaborate closely with other functions, including PR&D, Operations, Quality (QA/QC), SHE and external stakeholders/customers working towards the flawless, compliant and right first‑time manufacture of existing and new products. In addition, the successful candidate will provide mentorship, where applicable, to more junior analytical staff. Key responsibilities Carry out Analytical method development, specifically for HPLC and GC. Perform analytical testing in a timely manner for analytical method development, analytical testing, validation and qualification, where appropriate, to ensure project deadlines are achieved for: Campaign support, Material release, PR&D support (development of in‑process control methods, familiarization experiments), Reference standard qualification, Analytical investigations. Prepare, review and execute analytical protocols. Prepare and review analytical reports. Ensure all documentation is completed to the required standard, right first‑time, in compliance with local procedures and in a timely manner. Ensure all instrumentation used is within calibration and is correctly maintained. Liaise with AR&D Senior Analytical Chemists to obtain technical support with instrumentation/analytical methodology and laboratory investigations/quality events or related issues. Ensure training is completed before execution of a task. Attend weekly team meetings and participate in a culture, which is committed to high performance, innovation, and continuous improvement and promotes idea sharing. Meet with manager to discuss performance, provide feedback and identify any development opportunities. Ensure CGMP Compliance of laboratory operations and documentation, including testing, write‑ups, review and approval of protocols, reports and change controls. Ensure a safe work environment for oneself and all employees. Ensure high standards of housekeeping are maintained in the laboratory. Required Key Skills and Experience Ideally a BSC/MSc in analytical chemistry or equivalent. Preferably a minimum of 3‑5 years’ experience in analytical activities and analytical method development within a pharmaceutical manufacturing environment. Demonstrable expertise in developing analytical methods, particularly for HPLC and GC. Excellent core competencies such as teamwork, communication skills, technical writing skills. Strong technical background in chemistry, particularly analytical chemistry. Ability to work to tight timelines. Good Troubleshooting skills. Openness to change, receptive to new ideas. Knowledge of FDA and European GMPs requirements, particularly pertaining to laboratory operations. #J-18808-Ljbffr
SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state‑of‑the‑art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver life‑changing therapies that improve patient outcomes and save lives’. The facility located in Swords, Co Dublin, Ireland has led the way in the development, scale‑up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we have made some of the world’s most important medicines and continue to do so. Further information on SK pharmteco can be found at www.skpharmteco.com. Current Need SK pharmteco facility located in Swords, Co Dublin are looking to hire an Industrial Hygienist to provide support to its manufacturing operations and support Departments. Position Description The successful candidate will be part of the SHE team on site and report directly to the SHE Director. Highly motivated. Mindset of continuous improvement. Problem Solver – uses a scientific approach, data driven, customer focused. Comfortable with complexity. Sets out the standard required and demonstrates leadership in all aspects of programme delivery. Excellent report writing skills. Deliver results and improvement projects on time and in full. Self‑starter, capable of working on their own initiative and also as part of a team. Good collaboration & communication skills – comfortable explaining technical complexity. Participate in & lead continuous improvement projects within the SHE Department and across site. Flexible and willing to support other priorities within the Department as needs arise. Key Responsibilities Potent Compound Exposure Monitoring & Containment Verification: Develop plans, manage/coordinate and deliver a site IH chemical monitoring plan. Conduct IH monitoring and prepare reports. Communicate results and manage IH database. Ensure a regular programme of equipment and facility validation takes place to verify containment. Audit compliance. New Product Introduction (NPI) Support: Provide written assessments and banding recommendations on projects submitted for assessment. Work closely with NPI Projects group on confirming factory and equipment fits. CLP Directive & Chemical Compliance: Complete regular assessment & audits of site chemical inventories. Create awareness on compliance across site and at Leadership level. Collaborate with relevant Departments in driving the change(s) required. Labelling compliant. Audit compliance. REACH Directive & Chemical Compliance: Regular assessment & audits of site compliance with NPI and changes of chemical inventory and ensure compliance. Liaise with external parties as required. Create awareness on compliance across site and at Leadership level. Work closely with Supply Chain & Warehouse in particular. Ergonomics Programme: Develop plans, manage/coordinate and deliver on all aspects including manual handling training, DSE assessments. Complete ergonomic & MH assessments. Projects Support: Work with the Projects Department & other Departments to assess all aspects of new equipment introduction/facility design to ensure compliance or any changes/modifications to existing plant & equipment. Hazard Communications Programme: Ensure that MSDS are available for all substances and collaborate with various Departments including Supply Chain to ensure they are compliant. Audit compliance. Dangerous Goods Transport Programme: Oversight of programme and audit compliance. Work closely with Supply Chain. Respiratory Protection & Hearing Conservation Programmes: Oversight and coordination of required activities and ensuring both programmes meet compliance requirements. Audit compliance. Laser & Safety Programme: Compliance oversight and act as Laser Safety Officer (LSO). Audit compliance. Radiation Safety Programme: Manage our licence compliance obligations. Compliance oversight and act as the site Radiation Protection Officer (RPO). Audit compliance. General SHE Support: Provide SHE support and act as SHE point of contact with designated Departments. Act as the SHE point of contact on incident investigations, near misses, change controls and other management system programmes/processes. Asbestos Control Programme: Act as SME and liaise/collaborate with various Departments. Legionella & Biological Safety: Act as the compliance SME and participate in the cross‑functional management team. Ensure legal requirements such as the required Site Risk Assessment are kept up to date. Advise management and system owners of their duties and requirements. Audit the programme and prepare reports. SHE/IH Programme Training: Generate new materials and update existing training materials. Deliver initial & refresher training for all the programmes within scope of the IH programme and listed above. Occupational Health Programme: Work closely with the Occupational Health team in completing assessments and provide SME advice/direction on new chemicals introduced into the Plants and associated exposure controls put in place to ensure safe handling. Ensure the site First‑Aid programme is maintained with the current compliance standards required. Audit Occupational Health programme compliance. Other duties that arise. Flexible outlook and growth mindset. Minimum Requirements Degree in a scientific discipline – B.Sc . or higher. Qualification in Industrial/Occupational Hygiene or working towards obtaining certification. Competent to act as Subject Matter Expert (SME) in Industrial/Occupational Hygiene which requires assessing hazards and providing direction on measures or otherwise required to. Experienced in completing occupational/industrial hygiene exposure assessments. Pharmaceutical manufacturing experience. Experience of assessing the handling and containment of Highly potent Active Pharmaceutical Ingredients (HPAPI). Comfortable & knowledgeable with complex Chemistry. Experienced in developing IH sampling plans and conducting IH field sampling. Desired/Advantageous Qualification or training in Occupational Toxicology. Experienced in working on the containment and qualification of new plant and equipment. Ergonomic Assessments/DSE Assessments. Experience of liaising with Regulatory Authorities and Auditors. Other Benefits Excellent opportunities for career enhancement and personal development. Competitive base salary. Annual bonus linked to business results. A well‑established further education program. Pension scheme. Private Healthcare. SK pharmteco SM Europe is an equal opportunity employer. #J-18808-Ljbffr
SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver life-changing therapies that improve patient outcomes and save lives’. The SK pharmteco Small Molecule, Europe, facility located in Swords, Co Dublin, Ireland has led the way in the development, scale-up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we have made some of the world’s most important medicines and continue to do so. Further information on SK pharmteco can be found at www.skpharmteco.com Current Need: CPL in partnership with SK pharmteco Ireland are looking for a QC Instrumentation Specialist for a 12 month contract position. This position is in the Instrumentation group in QC Department. Position Description: Reporting to the QC Team Lead, the successful candidate will manage and control the laboratory instrumentation calibration and unplanned maintenance programme for the QC department. Responsibilities: Liaising with Agilent to co-ordinate the calibration schedule. Review all Laboratory Calibration/Qualification documentation. Review all equipment unplanned maintenance reports. Manage changes to instruments, instrument relocations and decommissioning of instruments. Troubleshooting laboratory equipment. Manage the purchase of new instruments and related installation operation qualification reports that are required. Manage laboratory instrument change controls. Develop new procedures and ensure equipment procedures are up to date. Conduct all instrumentation calibration investigations. Support the implementation and qualification of analytical instruments, and in their routine/periodic maintenance. Ensure GMP Compliance of laboratory operations and documentation. Managing equipment supplier relations for new equipment and software to be used in the laboratory. Foster and support a culture of growth, enablement and high performance. Qualifications: A BSc in Analytical Science, Chemistry or a related discipline is required. A minimum of 3 years’ experience working in the pharmaceutical industry is required. Knowledge of quality control operations. Experience of regulatory agency audits and an understanding of laboratory GMP’s FDA regulations and their application to API manufacturing. The successful candidate will be required to prepare for and participate in Regulatory and Customer audits. Experience in Equipment Validation and the change control procedures is desirable. The successful candidate will have a strong ability to manage their own workload (multiple tasks or projects, prioritise work, and ensure timelines are met for equipment calibrations, maintenance, and testing) and will interact with QAS, IM and with multiple vendors. The desired candidate should be highly motivated, have strong teamwork skills, with proven success of working in a team environment. #J-18808-Ljbffr
SK pharmteco is a global Contract Development and Manufacturing organisation (CDMO) with state-of the-art facilities in Korea, US, France and Ireland. We are part of SK Inc., a Korea company with revenues of $99 billion in 2023. Our mission is to ‘produce and deliver life-changing therapies that improve patient outcomes and save lives’. The SK pharmteco Small Molecule, Europe, facility located in Swords, Co Dublin, Ireland has led the way in the development, scale‑up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we have made some of the world’s most important medicines and continue to do so. Further information on SK pharmteco can be found at at www.skpharmteco.com SK pharmteco Small Molecule, Europe, facility located in Swords, are seeking to recruit a Project Manager on a 12 month contract to join the Engineering Department, reporting to the Engineering Programme Manager. They have a number of in‑house capital projects to be implemented over the next 12 months. An internal team will manage the projects from conception to completion and as part of this team a requirement has been identified for the role of project manager. The role will involve managing a number of site based capital projects involving design, construction, commissioning and handover. The role will primarily involve conceptual and detailed design support and co‑ordination, project budget and schedule management, project resource and contractor management, equipment procurement, interfacing with Maintenance, EHS, Quality and Operations Depts. Responsibilities Manage all phases of capital projects from concept through to implementation and close‑out. Manage design, construction, commissioning and qualification, project schedule and cost. Maintain a strong safety culture and performance in the implementation of capital projects. Ensure successful delivery of projects which meet business needs. Deliver cost effective projects in line with our project management procedures and best practices. Developing and maintaining collaborative relationships with stakeholders. Identify effective & innovative engineering design solutions which meet project client / end user requirements. Plan and lead the delivery of projects which meet all regulatory requirements including safety, quality and environmental requirements. Ensure that equipment qualification activities are completed in line with local procedures, cGMP and best practices. Develop and improve new and existing standards within the engineering department improving the service offered to clients/end‑users. Generate and manage project schedules to plan and track project activities over the life‑cycle of the project. Manage project risk registers with appropriate monitoring and tracking of mitigation actions agreed. Manage multi discipline project stakeholder input as required for successful project delivery. Required Qualifications and Skills Candidates should hold at minimum a Bachelor’s Degree in Engineering (Mechanical, Chemical, Process) and at least 5 years capital project management experience in the Pharmaceutical industry. Excellent communication and organisational skills with demonstrated capability to effectively communicate with all levels of the organisation is required. Ideally experience at an API manufacturing site (e.g. experience with piping systems, drying systems, HVAC, utilities, reactors, centrifuges, vacuum, heat/cooling systems etc) #J-18808-Ljbffr
SK pharmteco, part of SK Inc, is a global Contract Development and Manufacturing organisation (CDMO) with state‑of‑the‑art small molecule manufacturing facilities in Korea, US, and Ireland. The SK Small Molecule Europe facility located in Swords, Co Dublin, Ireland has led the way in the development, scale‑up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we make some of the world’s most important medicines. Further information on SK pharmteco can be found at www.skpharmteco.com Current Need: The Quality team are seeking to recruit a Quality Control Senior Analyst to join the QC Department reporting to the QC Team Lead. Position Description: Reporting to the QC Team Lead, the successful candidate will be involved in the testing, review and release of raw materials, intermediates, and active pharmaceutical ingredients, in the Quality Control Laboratory. The QC Senior Analyst will: Provide technical support for instrumentation and analytical methodology and execute trouble‑shooting. Provide coaching and training for instrumentation and analytical methodology within the QC laboratory. Plan and approve materials to meeting shipping and production timelines, stability timelines and Quality Control metrics. Co‑ordinate and lead laboratory/site investigations. Identify and investigate out of trend / adverse results present in analytical results. Working as part of a Lean Lab team‑based structure, the QC Senior Analyst will require excellent interpersonal and communication skills. The role will involve the use of the classical analytical technologies including Raman, FTIR, KF, in addition to a broad range of modern analytical techniques including HPLC, GC, ICP‑AES, ICP‑MS, and wet chemistry techniques. The QC Senior Analyst will also be required to engage and fully participate in daily huddle meetings and short interval control boards. Minimum Requirements: BSc in Analytical Science, Chemistry or related discipline is required. Minimum of 3 years’ experience in analytical chemistry is required. The desired candidate should be highly motivated, have strong teamwork skills, with proven success working in a team environment with flexibility to react to changing business needs. Experience in Operational Excellence, 5s, Lean Labs, yellow belt certification and yellow belt projects is desirable. The successful candidate will have a strong ability to manage their own workload and will play an important part in the various sub teams in QC such as Safety, Equipment, or Audit Readiness. Other Benefits include: An excellent opportunity for career enhancement & development. Competitive base salary. Annual bonus linked to business results. A well‑established further education program. Pension scheme. Private healthcare. SK pharmteco SM Europe is an equal opportunity employer #J-18808-Ljbffr
SK pharmteco, part of SK Inc, is a global Contract Development and Manufacturing organisation (CDMO) with state‑of‑the‑art small molecule manufacturing facilities in Korea, US, and Ireland. The SK Small Molecule Europe facility located in Swords, Co Dublin, Ireland has led the way in the development, scale‑up and commercial manufacture of Active Pharmaceutical Ingredients (APIs) and Chemical Intermediates for over 60 years. With a talented workforce, exceptional technical capabilities and facilities we make some of the world’s most important medicines. Further information on SK pharmteco can be found at www.skpharmteco.com Current Need: SK pharmteco Ireland are seeking to recruit a highly experienced Principal Scientist to lead a team in the process R&D group. We are seeking a highly skilled and motivated Principal Scientist / Chemist to join our Process Development team within a dynamic CDMO environment. The successful candidate will lead the development, optimization, and scale‑up of robust, safe, and cost‑effective chemical processes for the manufacture of Active Pharmaceutical Ingredients (APIs) and intermediates, from clinical through commercial stages. This is a senior‑level role that demands both technical expertise and leadership capabilities, with opportunities to mentor junior scientists and interface directly with clients and cross‑functional teams. As a Principal Scientist in API Process Development at our SK Pharmteco site you will play a key leadership role in delivering high‑quality, innovative solutions for our global clients. This role combines deep expertise in API process development with a passion for adopting cutting‑edge technologies to drive efficiency, quality, and scalability across diverse development programs. You will be responsible for leading the design, development, and scale‑up of chemical processes for small‑molecule APIs, while evaluating and implementing new manufacturing technologies such as continuous flow processing, process analytical technologies (PAT), and digital process optimization tools. You will act as both a technical expert and a client‑facing scientific leader, helping ensure successful development, technology transfer, and GMP manufacturing within tight timelines and regulatory frameworks. Primary Responsibilities Lead end‑to‑end development of API processes from route scouting through scale‑up and GMP manufacturing for client programs across clinical and commercial phases. Collaborate with clients and internal stakeholders to define development strategies, technology selection, timelines, and deliverables. Evaluate and implement innovative process technologies to improve yield, robustness, scalability, sustainability, or cost‑efficiency, including: Continuous flow chemistry Crystallisation development Advanced automation and real‑time data analytics PAT tools and real‑time release testing Green chemistry principles and solvent reduction Contribution to successful technology transfer into the site from clients or partner organisations, and from development to manufacturing. Serve as the scientific lead in troubleshooting process issues during familiarisation, optimisation and scale‑up, ensuring rapid and compliant resolution. Perform risk assessments, identify and mitigate potential scale‑up or safety issues (e.g., thermal hazards, exothermic reactions). Develop and implement Design of Experiments (DoE) to optimise critical process parameters. Collaborate closely with internal cross‑functional teams including Analytical, Quality Assurance, Tech. transfer, Manufacturing, Engineering, Supply chain and SHE. Author and review technical documentation, including process development reports, risk assessments, and CMC regulatory submissions. Stay current with emerging trends and technologies in chemical process development and apply them strategically to enhance client offerings. Mentor and develop scientists within PR&D and contribute to a culture of innovation and continuous improvement. Qualifications Education Ph.D. in Organic Chemistry, Chemical Engineering, or a related discipline. M.Sc. with significant industry experience will also be considered. Experience 8–12+ years of relevant experience in pharmaceutical API process development, preferably in a CDMO or fast‑paced multi‑client environment. Proven track record in process scale‑up, technology transfer and GMP manufacturing. Strong understanding of CDMO operations, client engagement, and regulatory expectations (e.g., IND, IMPD, NDA, MAA submissions). Strong technical experience in new technologies (flow chemistry, PAT, automation, etc.) and leadership in implementing new technology projects. 5 years’ experience leading teams in the delivery of complex process development projects. Key Skills & Attributes Strategic scientific and technical leadership across diverse projects and molecules. Effective communicator with a track record of building strong partnerships with internal stakeholders and external clients. Experience managing client expectations and highly skilled at translating complex technical progress into concise updates. Deep knowledge of synthetic organic chemistry or chemical engineering principles applied to scalable API manufacturing. Experience applying QbD and risk assessment tools as part of process development to meet regulatory expectations. A strong collaborative mindset with a willingness to take ownership and ability to thrive in a dynamic, client‑driven environment. Other Benefits include An excellent opportunity for career enhancement & development. Competitive base salary. Annual bonus linked to business results. A well‑established further education program. Pension scheme. Private healthcare. SK pharmteco SM Europe is an equal opportunity employer #J-18808-Ljbffr
