Cpl in partnership with SK pharmteco are seeking to recruit anAR&D Analytical Chemist for a 12 month contract onsite in the Swords Campus. 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 AnalyticalChemist 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: Campaign support Material release R&D Chemistry lab work (use-tests, familiarisation experiments) Material Stability program 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 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 and HPLC. 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: GMP HPLC API manufacture chromatography small molecules
Join the Naval Service as a General Service Recruit Please note: Interviews and fitness testing will take place onsite at the Naval Base, Haulbowline Island, Cork. We are now recruiting for General Service Recruits to join the Naval Service. After completing 12 weeks of initial Recruit Training, you will progress through branch-specific training before qualifying as an Able Rate. This is your opportunity to be part of a professional and dynamic team that patrols and protects Irelands territorial waters. About the Role: General Service Recruits form the backbone of the Naval Service and begin their careers with a 12-week training course focused on physical fitness, discipline, and basic military and naval skills. Upon completion, you will advance to Ordinary Rate and begin branch-specific training in one of four areas: Seaman's, Communications, Mechanicians, or Supplies. Once qualified, youll be promoted to Able Rate and assigned to a Naval Service ship, where youll take part in a two-year sea rotation. Duties include general maintenance, boat operations, firefighting, damage control, and participating in naval boarding teams during drug interdiction operations. Further training opportunities are available for those who wish to specialise and advance their careers within the Naval Service. Requirements: Education: No formal education qualifications required Age: 1839 years on the closing date of applications Other Requirements: Must be an Irish or EU citizen. Must be of good character and pass security clearance Must meet minimum standards of medical and physical fitness Must complete all phases of the induction process, including interview, fitness test, medical exam, and Garda vetting Location: All assessments conducted at the Naval Base, Haulbowline Island, Cork. Salary & Benefits: Basic salary: €41,435 with annual increments (after training) Additional allowances for overseas service: Starting at €15,000 Apply now for the 2025 Naval Service intake #navalservicerecruitment25 Skills: 18-39 years Benefits: Paid Holidays Canteen Gym Parking Pension Educational assistance Permanent Health Insurance
External Job Description Job Summary (Summarize the primary purpose & key accountabilities of the job function.) Development and implementation of analytics for new API processes and technology in manufacturing sites. Provide technical support and leadership for supply assurance projects Job Responsibilities (Indicate the primary responsibilities critical to the job function.) 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 existin commercial API processes to support project teams, API sites (internal and external) and global technical groups. Investigate new technologies and analytical approaches Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines. Contribute to the analytical team program of continuous improvement. Ensure the ongoing safe and efficient operation of facilities. Qualifications/Skills: Education - Experience - Additional Requirements (Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications, and other job-related technical and managerial skills.) 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. A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project. Project management experience a plus here. The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results. Develops advanced ideas and guides their development into a final product. Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes. Excellent interpersonal skills and the ability to work in a collaborative, team driven environment. Excellent written and verbal communication skills. Specific Requirements for each Global Job Level* For Research Analyst (GJL060), 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. Skills: Analytical development data analysis Method validation
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: API Method Validation Method Development HPLC
Cpl in partnership with our Client Pfizer are seeking QC Analyst - ICC teams to join them at their state of the art site in Dublin, Grange Castle for a contingent 11 month fixed term contract. This is an on site role. What You Will Achieve You will be a member of Pfizers dedicated and highly effective quality control team. You will be responsible for activities involved in developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines. Your contribution in quality risk management will help us in commitment tracking, interpreting policies, manage site complaints and work directly with operating entities to provide process analyses oversight. Thanks to you, we will be prepared for all upcoming audits and inspections. You will be relied on to ensure that the quality assurance programs and policies are maintained and modified regularly. You will make sure that there are uniform standards worldwide and best practice sharing, which will help in fostering the achievement of company's mission globally. You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviors that will help us achieve our goal of providing the best to patients. How You Will Achieve It *Perform analysis on QC samples (raw material, In-process tests, intermediates and finished product) in line with Current Good Manufacturing Practices. *Adhere to good laboratory practices and housekeeping standards. *Assist in the generation and maintenance of quality procedures and reports. *Facilitate laboratory investigations and support associated product investigation. *Participate, and seek opportunities, in the areas of Right First Time, Continuous Improvement and 5S. Qualifications Must-Have *Third level Qualification in Science, Engineering or equivalent is preferred though not essential. *Some experience working in a QC Laboratory. *Demonstrate proven experience with analytical techniques including bioassay/potency testing, ELISA, blotting, flow cytometry assays, PCR, molecular biology techniques. *Excellent interpersonal and communication skills. *Detail oriented, quick at decision making, self-motivated with good trouble shooting and problem-solving abilities. Nice-to-Have *Experience in quality control in a biotech, pharmaceutical, or bio-pharmaceutical manufacturing environment. *Knowledge of computer applications, including MS Office, Excel, Softmax, Laboratory Information Management System (LIMS) and track wise. *Mammalian cell culture experience. *Aseptic techniques and sampling handling. 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. Shift work may be required for this role (extended days). Additional Detail * To be considered for this position you need to be legally eligible to work in Ireland. *Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. * Due to high volume of applications, we will be contacting successful candidates only. *We do not offer relocation. Candidates who complete the recruitment process and are selected as successful will be offered roles in specific teams within the QC - ICC space as QC Analyst depending on their skills, experience, and current vacancy requirements Skills: ELISA PCR molecular biology
QC Senior Analyst Location: Swords, Co. Dublin 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 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 troubleshooting. Provide coaching and training on instrumentation and analytical methodology within the QC laboratory. Plan and approve materials to meet shipping, production, and stability timelines, as well as QC metrics. Coordinate and lead laboratory/site investigations. Identify and investigate out-of-trend or adverse 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 involves the use of classical analytical technologies including Raman, FTIR, KF, in addition to a broad range of modern analytical techniques including HPLC, GC, ICP-AES, ICPMS, and wet chemistry. 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, with strong teamwork skills and proven success in a team environment, with flexibility to adapt to changing business needs. Experience in Operational Excellence, 5S, Lean Labs, yellow-belt certification, and yellow-belt projects is desirable. The successful candidate should be capable of managing their own workload and play an active role in QC sub-teams such as Safety, Equipment, or Audit Readiness 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: HPLC GC Karl Fischer
Engineering Program Manager CAPEX Projects (12-Month Contract) Location: SK biotek Ireland, Watery Lane, Swords, Co. Dublin Duration: 12 months (minimum) SK biotek Ireland has a number of in-house capital (CAPEX) projects to be implemented over the next 12 months. An internal engineering team will manage these projects from conception to completion, and as part of this team, a need has been identified for an Engineering Program Manager. This role will provide oversight and leadership for a group of project managers handling multiple site-based CAPEX projects involving design, construction, commissioning, and handover. The role will also include direct management of certain projects. The position requires close collaboration with the Maintenance, Safety, Quality, and Operations departments and will focus on conceptual and detailed design, budget and schedule management, contractor coordination, and equipment procurement. Key Responsibilities: Ensure the successful delivery of capital projects that meet business needs, following company project management procedures and best practices. Oversee and manage all phases of CAPEX projects from concept and design through implementation, commissioning, qualification, and close-out. Maintain a strong safety culture and performance throughout project implementation. Develop and maintain collaborative relationships with internal and external stakeholders. Identify effective and innovative engineering design solutions that meet end-user requirements. Lead projects to ensure compliance with all safety, quality, and environmental regulations. Ensure equipment qualification activities are completed in line with cGMP, local procedures, and industry best practices. Develop and enhance standards within the engineering department to improve services delivered to clients and end-users. Support project managers in planning and tracking project schedules across the full lifecycle. Manage project risk registers, monitor progress, and ensure mitigation actions are executed. Coordinate multidisciplinary stakeholder input to ensure successful project delivery. Qualifications and Experience: Bachelors degree in Mechanical, Chemical, or Process Engineering (minimum). At least 10 years of capital project management experience in the pharmaceutical industry. Proven experience overseeing a program of capital (CAPEX) projects, covering all project phases from concept to CQV and handover. Demonstrated ability to manage engineering design contracts and service providers. Strong background in project budgeting and scheduling. In-depth knowledge of CQV standards, workflows, and GMP best practices. Strong leadership skills with the ability to manage priorities in a dynamic environment. Excellent communication, teamwork, and organizational abilities, with experience engaging across all levels of the organization. About SK biotek Ireland: SK biotek Ireland is part of SK pharmteco, a global Contract Development and Manufacturing Organization (CDMO) with state-of-the-art facilities in Korea, the US, France, and Ireland. Skills: CAPEX API pharmaceutical industry
Cpl in partnership with Pfizer Grange Castle are looking to hireDS2 CQV Engineeron an 11-month contingent contract. Introduction: TheDS2 Projectis Design, Construction and fit-out of a multiproduct large-scale Cell Culture facility, including 6x bioreactors (13,200L), associated scale-up trains, support equipment, and a single purification suite to double existing site capacity. Forecasted demand of licensed and pipeline products exceeds the available capacity within the Pfizer Global Supply (PGS) network, hence the requirement for this project. Location: Grange Castle/A&E Firm (Jacobs, Dublin Office) Project Background: Construction on site is significantly advanced (PM Group as Construction Managers), with many systems now mechanically complete. Utilities and process equipment commissioning and qualification is underway. Purpose of the Role: Your role will primarily be execution of commissioning and qualification of process equipment and utilities that are within the DS2 project scope. There will be some development of the C&Q package of documentation. The job holder will provide technical expertise to ensure that systems, equipment, and processes are designed, installed, commissioned, and qualified to the agreed specifications. Reporting to the CQV Lead role is responsible to: * Perform shakedown andcommissioning and qualification of systems. * Participate in construction system completion walkdowns. * GenerateCQV documentsat project level and for specific equipment/systems. Liaising with Quality, Engineering and CQV to align on Critical parameters and document content. * Track and confirm closure of actions items identified fromwalkdowns, FAT, HAZOP, Design Qualificationand other reviews. * Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise. General Information: Job Title: DS2 CQV Engineer Department: DS2 Project Team Position Reports to: DS2 CQV Lead Education/Experience: To be successful in this role you will require: *B.Sc./B.Eng.degreeinengineeringdiscipline,withparticularemphasismechanicalorprocessengineering. * Minimum of 4 years experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment. * Demonstrated ability to work on own initiative and proactively respond to business needs. * Excellent interpersonal and communication skills. * Familiar withDelta-V&Navis Worksan advantage. Skills: Delta V Navis Works Commissioning walkdowns FAT HAZOP Design Qualification
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: Campaign support, Material release, R&D Chemistry lab work (use-tests, familiarisation experiments), Material Stability program, 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 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: HPLC GMP API IPC QC Analytical Chemistry Method Development
Cpl in partnership with our client Pfizer are seeking a Supply Planner to join the team for an 11 month fixed term contract at their Newbridge site. This is an onsite role for an initial 6 months - then hybrid working options available. Position Summary As the Material Planner, you will be responsible for overseeing and optimising the inventory control (IC) and Inventory Management (IM) activities. This role involves supporting monthly Demand plans, optimising production strategies, and integrating new businesses and products. You will facilitate the IC / IM processes, develop metrics for these processes, and ensure data integrity and Material/ Inventory performance. General Responsibilities 1. Ensure strict adherence to site policies/procedures, cGMP/GLP and environmental, health and safety regulations. 2. Ensure area of responsibility is maintained in a constant state of compliance and audit readiness in line with current regulations, PQS, and business needs.All related procedures and documentation are maintained accordingly. 3. Safety and housekeeping considerations 4. Execute responsibilitiesin line with Right First Time principles 5. Ensure resolution of and/or appropriate escalation of issues 6. Demonstrating company values and Pfizer competencies 7. Ensure that all department metrics are adhered to 8. Provide subject matter expertise and support for systems, technologies and products. 9. Identify Continuous Improvement opportunities and progress Continuous Improvement projects. 10. Participate in for decision making in consultation with relevant stakeholders 11. Support the introduction of new products. 12. Report to the department manager. Specific areas of responsibility Job specific accountabilities will be as per one or a number of the following dependent on role assignment within the department Customer Service Management support Customer order promising and communicating changes in availability dates in a professional and timely manner. Co-ordinate with internal manufacturing to ensure timely product availability whilst minimising supply chain inventories at NB and Market locations. (Batch tracker support) Manage ISS and SO markets (Open order reports) Key contact for escalations on supply issues from Markets. Data Management Assist with the creation and Management of Data loading in PT/ master data changes initiator Supplier data change management Ci Support(FG/ RM*) Work closely with Planner to identify waste, reduce it and list CI projects to elimination of Nonvalue activities and improve response. Work with CI specialist/ Ambassador to support team to complete CI initiatives. Track CI initiatives in the CI funnel (CI transformation plan) related to IC/ MM S&OP Support Metrics Support all S&OP and Demand Planning activities. Facilitate the monthly Material forecast aggregation process, ensuring consensus among functions and stakeholders. Establish and maintain best practices for data analysis Provide detailed performance on Materials (FG/ RM) inputs to Sales, Operations, Finance, and Supply Chain teams Develop and monitor metrics for Material forecast accuracy, planning data integrity, and overall S&OP Material performance Inventory Control Review and analyse forecast demand versus actual demand to understand changes and trends. Notify scheduling and manufacturing teams of significant forecast or capacity changes in a timely manner Support Pack PAR changes/ financial exposure Support PP processes through Supplier relationship Management (SRM) MRB support to track actions with relevant stakeholders Own with planners the ZDI process- support actions escalation for final disposition Manage Change control pertaining to the department Minimise financial exposure through inventory optimising processes PPGs & cGMP PPG development and maintenance. Maintain strict adherence to all plant PPGs Project Management Manage and partake in projects and assignments for continuous improvements. Participate in NPI projects, Transfers, Divestments, Obsolescence. Minimum Qualification Requirements Education: Third level Qualification in Purchasing/Materials Management or business/science related area is preferred. Exceptions may be considered where relevant experience and correct attitude and behaviour exist (this may be supplemented by further education in parallel). Experience: Minimum 2 years experience in Manufacturing Planning / Supply Chain / Logistics Attention to detail, accuracy in record keeping and documentation. Proficient in Microsoft Office Applications Clear communicator and solution orientated Ability to identify and gather information necessary for effective decision-making. Ability to effectively prioritise and handle multiple tasks Ability to coordinate project work as part of a team Service minded, reactive and rigorous. Skills: SAP Supply Chain Manufacturing Planning Logistics
