Cpl in partnership with our client Pfizer are seeking an Analytical Scientist to join the team for an 11 month contingent contract at their state of the art site in Grange Castle, Dublin. This is an onsite role. Analytical Scientist Working in a multidisciplinary analytical team you will contribute to the characterisation and analysis of therapeutic glycoproteins, mRNA and conjugate vaccines. Your role will be to provide analytical characterisation, new method and technology development, and technical support to several functional groups including Protein and Vaccine Process Development and pilot scale manufacturing operations, Commercial manufacturing, and the Quality and Regulatory units. This is what you can look forward to *Become expert in the application and development of analytical methods used for the characterisation and manufacturing support of therapeutic proteins, vaccines and small molecules. *Participate in cross-functional teams in support of late-stage development and commercial products. *Provide technical subject matter expert and investigative support to commercial manufacturing operations. *Participate in the technical writing and review of analytical documentation, and regulatory submissions and responses. *Evaluate, develop and qualify analytical technologies to support method improvements for use in analytical development and QC laboratories. *Provide analytical support to process development team in bench and pilot scale production of proteins and vaccines, including sample analysis and interpretation of results, as required. To be successful in this role you will need: *B.Sc. / M.Sc. or higher qualification in analytical biochemistry, chemistry, biotechnology or a related discipline. *3-5 years experience in analytical role in pharmaceutical industry, experience with biological products and/or vaccines an advantage *Technical capability in several major areas of analytical sciences such as: UPLC / HPLC (UV, FLR, CAD), MS, GC, spectrophotometry, bioassay, ELISA, FACS, wet chemistry techniques and capillary electrophoresis. Experience characterising glycoproteins, monoclonal antibodies and vaccines an advantage. Independent contributions as a Scientist through one or more of the following: *Demonstration of problem solving ability through independent contributions to analytical method development/qualification/validation programs. *Lead role in analytical investigative support. *Subject matter expertise in one or more analytical technologies. *Ability to independently plan and perform work assignments, interpret and present data. *Possession of technical problem-solving abilities and communication skills accredited lean/six sigma/DMAIC competency is desirable. *Capability of coordinating activities and delivering project goals working in a multi-disciplinary team environment. *An understanding of industry specific standards/ regulations e.g. ICH, GMP, Environmental, Health and Safety etc. *Demonstration of ability to interpret industry guidelines for execution of technology transfer and implementation of analytical method validations considered an advantage. *Experience in authoring/contributing to analytical aspects of regulatory submissions and agency responses. Skills: method development HPLC GMP analytical chemistry
Electronic Health Record (EHR) Application Support Analyst (Grade IV) This is an exciting time to join the new Electronic Health Record (EHR) team as an Application Support Analyst (Grade IV). This role will be varied, fast-paced and youll be part of a team dedicated to implementing the EHR for the new CHI hospital which is due to open in 2026. Purpose of the Role: CHI will work with Epic Systems, a software company who are a world leader in this technology, to implement an electronic health record (EHR) system across the organisation, which will go live at the same time as the new hospital opens as Irelands first fully digitalised hospital. The EHR Application Support Analyst (Grade IV) is a core member of the Electronic Health Record (EHR) team. The post-holder will assist the EHR design, configuration, testing and training during the implementation phase to HIMSS Level 6, and subsequently support the go-live and post go-live stabilisation phases. As part of this role the EHR Application Support will attend accredited EHR vendor training and receive certification in system configuration. This position would suit candidates from the following areas (experienced with skills or recent graduates): *ICT, eHealth, Software Engineering or Computer Science *Digital Health and/or eHealth *Nursing, Midwifery, Pharmacy, HSCP disciplines or Medicine (NCHD) *Operational or Administration Essential Criteria: Applicants must meet all the following: Experience *Minimum of one year's experience working in an Irish, UK or other European hospital in either: oA direct clinical care role, or oA patient administration or related support role within hospital services or *Equivalent experience using healthcare systems or electronic health record (EHR) applications within an Irish, UK or other European hospital Education *Have successfully achieved a Leaving Certificate or equivalent qualification (Level 6) within the QQI Framework and *A third-level degree or higher diploma or PLC relevant to the role Technical Skills *Demonstrated competency in Microsoft Office Applications (Outlook, Word, Excel, SharePoint) as part of day-to-day work Desirable Criteria: Experience working in an acute hospital setting in Ireland or another European healthcare system (experience within Childrens Health Ireland preferred) Evidence of Continuing Professional Development (CPD) in a relevant area. Clinical background as a: oPharmacist, Pharmacy Technician, HSCP, HCA or Registered Nurse Experience using technical or project tools, such as: oJira, Zephyr, or ServiceNow (or similar ticketing systems) Experience in supporting end users during system workflow changes or tool implementations, demonstrating strong interpersonal communication, effective issue resolution, and confidence in identifying or escalating solutions as needed. How to Apply and Informal Enquiries: Applications for this post must be accompanied by a cover letter, setting out relevant experience that illustrates how the essential criteria listed above is met. * Please note that you must submit a cover letter and CV, this forms part of your application. Applications will not be accepted without a detailed cover letter and CV. Please see full job description attached below. The closing date for submission of application is Friday 27th of February at 12.00 noon.Applications must be completed through the advertised post onby clickingApply for Job. Applications will not be accepted through direct email or any other method. For queries relating to this recruitment process, please contact the Recruitment team via email: Childrens Health Ireland is an equal opportunities employer. #LI-CB5 Skills: ICT eHealth patient administration clinical care
Cpl in partnership with Pfizer Grange Castle are looking to hire DS2 EHS Specialist on an 12-month contract. Purpose: At Pfizer, we are committed to upholding the highest standards of safety for both our patients and colleagues. As a vital member of the Environmental Health and Safety team, your role is crucial in maintaining these standards and ensuring the organization is prepared for necessary compliance activities. By adhering to these principles, you help us achieve our mission of delivering exceptional healthcare and fostering a secure workplace. What you will do: *Assurance of compliance with EHS legislation, industry standards, and corporate policies. *Promotion and development of an Incident & Injury Free safety culture on the project. *Actively participate in process operational risk assessments with multidisciplinary teams. *Monitor and drive completion of outstanding HAZOP actions related to chemical safety, PPE, and operational controls. *Collaborate cross-functionally to meet milestones such as Operational Readiness Reviews and equipment handover. *Track and manage completion of process walk-down and risk assessment actions *Support environmental compliance and support Industrial emissions licence actions. *Support incident investigations and implement Good Save Reporting Programme. *Communicate EHS performance via dashboards and metrics. *Manage audit and inspection programmes and review incident data for trends. *Develop and deliver EHS training for the project. Minimum Requirements: *BA diploma or relevant certificates in Environmental, Health and/or Safety areas. *5+ years of relevant experience. *Proficiency in understanding and applying the laws, regulations, standards, and best practices governing environmental, health and safety at work. *Strong verbal and written communication skills. *Good skills in managing digital systems and Microsoft Office Suite. *Ability to manage multiple tasks effectively. *Strong analytical and problem-solving skills. Nice to have: *Knowledge and experience managing technical aspects of EHS programs. *Knowledge in digital tools (SharePoint and/or EHS digital platforms). *Strong interpersonal skills and the ability to work collaboratively with cross-functional teams. *Good organizational skills and attention to detail. *Ability to adapt to changing priorities. *Ability to work in a fast-paced environment. Skills: Environment health safety programs EPA regulated environment
AR&D Analytical Chemist Cpl are seeking to recruit an experiencedAnalytical Chemiston site in Swords with SK pharmteco for a 12 month contract. Position Description 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 Analytical Chemist will be responsible for providing technical support for all aspects of analytical methodology, 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 R&D Chemistry, 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 include: Carry out analytical testing in a timely manner for analytical method development, analytical testing, validation and qualification, where appropriate to ensure project deadlines are achieved for: o Campaign support, o Material release, o R&D Chemistry lab work (use-tests, familiarisation experiments), o Material Stability program, o Reference standard qualification, o 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 GMP 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 include: Ideally a BSC/MSc in analytical chemistry or equivalent. Preferably a minimum of 4 years experience in analytical activities within a pharmaceutical manufacturing environment. 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. Skills: Analytical Chemistry GMP API Pharmaceutical
Chemical Process Operator Swords, Co Dublin Current Need: CPL in partnership with SK pharmteco Ireland are looking for a Chemical Process Operator on a 12 month contract. The Chemical Process Operator is responsible for all tasks associated with the manufacture of Active Pharmaceutical Ingredients (API) and the operation of an API plant. This is a shift role working on a four-shift cycle supporting a 24/7/365 world-class manufacturing organisation. Position Description: Handling of chemicals to manufacture chemical intermediates and active pharmaceutical ingredients. The preparation and monitoring of equipment used for batch manufacturing and cleaning. Support Operational Excellence and other departmental projects as appropriate. Ensuring the plant is in an audit ready state and that plant operations are executed in a safe manner and to expected cGMP standards. Participate on site emergency response team (if required). The use of business systems for carrying out real time data entry and transactions for operations within the shift, e.g. SAP, IT & Delta V systems. Play a key role in meeting plant key performance indicators such as throughput, yield, safety, quality and changeover targets. Minimum Requirements: Have a relevant qualification in Chemistry/Chemical Engineering/ other science discipline or previous experience (4 + years) working within the pharmaceutical industry. API/small molecule experience a distinct advantage. Possess good interpersonal and communication skills, with a proven ability to troubleshoot and problem solve. Have strong collaborative skills with an ability to work effectively in a team environment or on ones own initiative without close supervision. Skills: Chemical Process Operator
Cpl In partnership with our client Pfizer are seeking a QC Analyst Micro to join the team for an 11 month fixed term contract, Onsite at their state of the art plant in Dublin, Grange Castle. this is an Onsite role. Job Responsibilities: Perform Microbiological testing analysis on, but not limited to, finished drug product, in process materials, stability samples and environmental monitoring. Responsible for calibration and use of laboratory instrumentation. Complete documentation associated with analytical results in a timely manner. Report and document any non-conformances to the QC Manager. Assist in the preparation and review of area documentation e.g. SOP's, Reports, Protocols. Assist in the training of other analysts. Ensure training compliance within assigned work area and QC. Perform and assist in additional duties as directed by the QC Manager. Ensure relevant assays are performed on samples in support of release test and stability test programs. Support any validation and qualification of test methods and processes. Facilitate laboratory investigations and support associated product investigation. Support Laboratory inspection and audits. Troubleshoot laboratory methods and instrument problems. Establish and monitor trend analysis program. Contribute to the operations of the Quality Control Laboratories. Liaise with all customers both internal and external. Record and review laboratory testing documentation to cGMP standard. Implement and adhere to appropriate levels of cGMP within the laboratory. Promote safety awareness and the established culture of IIF within the assigned work area. Ensure that sample analysis is conducted to meet batch disposition requirements. To be successful in this role the following are prerequisites to application: Third level Qualification in Science, Engineering or equivalent is preferred though not essential.Exceptions may be considered where relevant skills/experience and correct attitude and behaviours exist (this may be supplemented by further education in parallel) Excellent communication and interpersonal skills This job description indicates the general nature and level of work expected of the incumbent.It is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities required of the incumbent.Incumbents may be asked to perform other duties as required Skills: Bioburden testing Microbiology Environmental testing
AR&D Analytical Chemist Cpl are seeking to recruit an experiencedAnalytical Chemiston site in Swords with SK pharmteco 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). The Analytical Chemist will be responsible for providing technical support for all aspects of analytical methodology, 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 R&D Chemistry, 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 include: Carry out analytical testing in a timely manner for analytical method development, analytical testing, validation and qualification, where appropriate to ensure project deadlines are achieved for: o Campaign support, o Material release, o R&D Chemistry lab work (use-tests, familiarisation experiments), o Material Stability program, o Reference standard qualification, o 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 GMP 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 include: Ideally a BSC/MSc in analytical chemistry or equivalent. Preferably a minimum of 4 years experience in analytical activities within a pharmaceutical manufacturing environment. 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. #LI-NC3 Skills: Method Development Method Validation HPLC
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 worlds most important medicines and continue to do so. Further information on SK pharmteco can be Current Need: Our Business Excellence Team are looking to recruit a Business Intelligence Analyst to join our team based in Swords, Co. Dublin on a temporary (contractor) 12-month basis. Overview: As a member of the Operational Excellence and Digital Transformation team, you will serve as a BI/Data Analyst and support on multiple digitalisation projects' implementation, playing a pivotal part in designing, developing, and implementing digital solutions contributing to our overall site strategy. The role involves integrating digital technology into all our business areas, empowering our business leaders to streamline their processes, increasing operational efficiencies, and driving growth through low-code automation and data-driven solutions. To achieve this, you will collaborate closely with cross-functional teams, including department managers and SMEs across all areas of our business, such as Safety & Environmental, Operations, Quality, Engineering, R&D, Supply Chain, Project Management, Finance, Strategy and Operational Excellence; and you will support the mapping of current manual and time-consuming processes, propose, and deploy digital solutions. This position provides opportunities to learn and develop business and interpersonal skills, as well as a deep understanding of the industry. Main Activities & Responsibilities: *Collaborate with cross-functional teams to understand business requirements and translate them into effective data visualisations, reports and visually appealing Power BI dashboards that drive actionable insights to various stakeholders. * Develop and implement custom solutions and Automate workflows and business processes using MS-365 and Power Platform, such as Power Bi, Power Apps and Power Automate. * Implement best practices for data modelling, transformation, and aggregation; Ensure availability and reliability of data sources, troubleshoot technical issues. * Lead and support the implementation of digitalisation projects such as Data analytics platform, AI tools/solutions, Data Lake, Electronic Batch Record (EBR), among others. * Contribute to data governance and document data strategy; * Assist in project documentation, solution validation, SOP updates, create work instructions, training materials and presentations. * Collaborate with vendors and partners to identify technical solutions, create detailed business requirement documents, use cases, functional specifications and develop technical documentation and training materials Requirements: *Bachelors Degree in STEM, Business, Supply Chain, or related field with specialisation in Business/Data analytics, or equivalent experience. * Minimum 3 years of experience in Data Analytics or Business Analytics with strong hands on delivery using Microsoft Power BI, including data ETL, Power Query, report and visualization development, and DAX calculations and row level security. * Experience managing Power BI Service environments, including workspace administration, access control, role based security, deployment pipelines, dataset refresh scheduling, and lifecycle management across workspaces. * Desirable experience with Microsoft Fabric Lakehouse, including Data Pipelines and medallion concept. * Preferred hands on experience with Microsoft Power Platform, including Power Apps and Power Automate, with a focus on automation and process enablement. * Strong proficiency in SQL and relational database technologies, and working knowledge of integration patterns and API based data access. * Experience with SAP Hana reporting automation is an advantage. * Experience in life science sector, GMP solutions deployment and validation and FDA's regulations for electronic documentation (FDA 21 CFR Part-11) will be a distinct advantage. * Understanding of Operational Excellence Concepts and Continuous Improvement Methodologies, with a Yellow Belt or Green Belt certification, or demonstrate a willingness to pursue certification upon joining the team. * Strong analytical and technical skills, proficiency in Microsoft Excel and PowerPoint. * Excellent communication skills and the ability to work in a cross functional collaborative environment Skills: SQL Power Apps
Cpl is a proud Talent Partner to Bank of Ireland. We have been a trusted partner to deliver brilliant, engaged and committed people to support Bank of Irelands promises to deliver for their customers. Cpl trust that Bank of Ireland offers a fantastic opportunity for our Cpl Colleagues to learn, develop and build their career within banking and receiving access to the best training, systems, and support from our colleagues in Bank of Ireland. Our goal is that while you are a Cpl colleague on site with Bank of Ireland, you are set up for success no matter what your role, duration, or terms of your contract. This role will provide full 360 support to you by way of full training, and on-going support to develop yourself. This is an environment where the customer is the focus, and as a Cpl colleague on site with this client, you will be central to that delivery. At the heart of this purpose is our commitment for an inclusive environment. What is the opportunity? This is an exciting opportunity for an ambitious and self-motivated individual who would like to build their skills and progress their career within Bank of Ireland. Working as part of a dynamic and supportive team you will have the opportunity to work closely with our personal and business customers. Roles available: At the moment, we have roles available in the Oldcastle, Co Meath branch that will require occasional travel to both Bailieborough and Cavan Town. In this role, you will: Engage with customers to deliver a professional, efficient and friendly Customer Service (including Cashier Service where appropriate) to Business and Personal customers Handle the flow of customers to ensure their smooth passage through the Branch Relocate customers to appropriate self-service options - including on-line and Banking 365 delivery channels together with demonstration of self-service facilities Record/update relevant customer information on in-house systems Handle all basic queries/problems and refer complaints as appropriate Bring customer insights into our decision making and have the means to be confident in our ability to deliver appropriate outcomes for our customers Understand your goals, and your role in delivering and achieving the Group`s shared ambitions Act with integrity and learn from successes and mistakes to foster an environment of continuous improvement to perform at our best; and we recognise those who contribute to the Group`s success Demonstrate openness and willingness to change. We embrace change as a key strategic enabler and actively seek to enable the timely implementation of efficient and robust solutions! You may occasionally be required to carry and handle money, including transporting cash and ensuring its secure delivery. This task will be conducted in accordance with established security and safety procedures What will make you stand out? A proven record in delivering an outstanding customer service, demonstrating excellent communication and interpersonal skills with an ability to work efficiently as part of a team. Self-motivated with a passion to achieve goals and identify sales leads and referrals. You have a curiosity for technology, and are an early adaptor of new technologies. The willingness to learn and grow your career within the company! Essential Qualifications There are no essential qualifications required for this role. Cpl is committed to providing a positive employee experience for all its people where everyone can gain access to meaningful and challenging work with opportunities for growth and career progression. Cpl is an Equal Opportunity employer. At Cpl we believe that delivering our vision to be the worlds best at transforming our clients and candidates through sustainable transformational talent solutions & experiences can be achieved by having a diverse and inclusive culture, where everybody feels that they can bring their whole selves to work and are proud to do so. Cpl welcomes applications from all individuals, including applicants with additional needs and disabilities and those who have taken time out for reasons including family or caring responsibilities. As a company Cpl is a Gold Medal holder for Diversity & Inclusion. We have also been recognised as the 5th Best Large Workplace in Ireland by Great Place to Work; these values drive our passion for our programs, supporting our clients and Cpl colleagues across our client sites. #BOICpl2025 Benefits: Educational assistance
ABOUT US 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 worlds most important medicines and continue to do so. Further information on SK pharmteco can be Current Need The R&D Team at the Swords Campus are looking to recruit a Senior Technology Transfer Process Engineer to join the R&D Department reporting to the Associate Director, Technology Transfer. Position Description Reporting to the Associate Director, Technology Transfer the successful candidate is responsible for leadership and execution of technology transfer activities for new product introductions within R&D. They will be focused on the successful introduction of new products to the Swords site, leading multiple, complex tech transfers simultaneously (small molecule, HPAPI, or peptide) into manufacturing. The role ensures seamless scale up from lab/pilot to commercial scale, ensuring process robustness, GMP compliance and repeatable product quality. Key Responsibilities and Attributes Working as part of a cross functional technology transfer team comprised of process chemists and engineers, the Senior Technology Transfer process engineer should have the following attributes: Core Skills and Competencies Core competencies of leadership, excellent communication skills, teamwork, problem solving particularly with external customers Strong project management and organizational skills Commitment to the SK biotek values, compliance and continuous improvement Technical Expertise A high level of expertise in technology transfer, API pharmaceutical manufacturing, plant operations and engineering projects is essential Subject matter expert for chemical process engineering (reaction kinetics, mass transfer, scale up, crystallization, isolation, drying) Ability to interpret process data, analytical results and development reports, communication of findings and recommendations to management and customers A high level of proficiency with process engineering tools eg Dynochem, Computational Fluid Dynamic software is desirable A good knowledge of regulatory and safety guidelines is necessary Leadership and Stakeholder Management Ability to lead multiple cross functional teams and drive decision making internally and with customers High technical credibility and ability to influence decisions Strong negotiation skills with clients and internal stakeholders Strategic thinking, systems-level understanding of successful technology transfers Problem Solving and Adaptability Exceptionally strong investigation and root-cause analysis capability Adaptability in a fast paced CDMO environment with multiple concurrent projects Demonstrated ability to drive change Specialised Experience (Advantage) High Potency API containment strategy for OEB5 compounds, closed system handling, occupational exposure control strategies, facility upgrades Peptide manufacturing design of scalable peptide synthesis strategies, chromatography/lyophilization expertise, technical troubleshooting of complex impurity profiles Requirements A minimum of an honours degree in chemical or process engineering or a related discipline is required A minimum of 710 years experience in the bulk pharmaceutical industry with technology transfer experience is required The desired candidate should have experience leading cross functional, customer facing teams with a strong working knowledge of relevant cGMP, safety and environmental regulations Other Benefits Include 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 Insurance Skills: High Potency API CDMO
