Salary: Competitive / Based On Experience Reporting To: Senior QC Analyst Reference: VER_2213 Introduction Join an exciting new Irish Company supporting researching and development in the pharmaceutical sector. Arbutus Innovation Centre is advertising this position on behalf of Verbena Limited based in Athlone. This is an exciting opportunity to work in a fast-paced environment with a small, collaborative and dynamic team of innovators and experienced leaders. This role come with ample opportunity for true opportunity for growth. JOB PURPOSE To prioritise, sample, test and release client test requirements, intermediates and finished products. Operative needs to ensure that strict timelines are met, in‑line with supporting the business needs and requirements. To support the new formulations /finished products stability programme. RESPONSIBILITIES Sampling and testing of raw materials, intermediates and finished products using current pharmacopoeias, any associated ‘wet’ chemistry and instrumental techniques (HPLC, LC‑MS, GC‑MS, IR, UV), as appropriate. Preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports. Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods. Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, GC‑MS) techniques, as appropriate. Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specifications. Writing/reviewing Standard Operating Procedures (SOPs). Calibrating analytical equipment, as and when required. Supporting all QC activities. Ensuring that procedures are carried out carefully and accurately to eliminate errors. Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers. Working with all members of staff to maintain and develop the positive progressive culture within the organisation. Observing and complying with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). Observing and complying with company Health and Safety Policies. Observing and complying with company Standard Operating Procedures (SOPs). Undertaking any other duties, either for this department or any other department within the business, which may be requested by the Line Manager, for which training and/or an explanation has been provided and understood. PERSON PROFILE: Degree in a scientific discipline (with strong chemistry content). Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level. Highly proficient in the use of key analytical equipment (HPLC, IR, UV) and the testing of finished products. Experience of working in a GMP environment. Good IT skills e.g. Microsoft Office (Word, Excel and Outlook). Credible and confident communicator (written and verbal) at all levels. Highly customer focused and passionate about delivering excellent customer service. Ability to achieve and maintain high standards with meticulous attention to detail. First class planning, organisational and time management skills. Ability to work accurately in a busy and demanding environment, adhering to strict deadlines/timescales. Strong analytical and problem solving ability. Self starter who can ‘hit the ground running’. First class team player with a totally flexible approach. Self motivated with the ability to work proactively using own initiative. Hands on approach with a ‘can do’ attitude. Committed to learning and development Experience: Minimum Two years of HPLC experience. Understand, internalise and apply cGMPs and cGLPs; knowledge of laboratory processes. Effective interpersonal skills, written and oral communication skills; organisation skills and detailed-oriented, effective computer skills (Microsoft Word and Excel). Knowledge of laboratory analyzers and equipment used to perform chemical analyses. Able to work as part of a team Due to the nature of this job, fluency and an excellent command of the English language is an absolute must – both written and spoken. What We Offer Strong Opportunity for growth Opportunity to learn and grow across departments Flexible working options Additional Information To be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position. Equal Opportunity Employers We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Arbutus Innovation Centre and its client companies are committed to celebrating this, in all its forms. We strive to build a culture that encourages, supports and empowers our employees. Competitive Salary & Benefits: Interested candidates should submit an updated CV and cover letter to: careers@arbutus.ie IRELAND Daneswell Business Park Monksland, Athlone Co. Roscommon Republic of Ireland Contact Us If you have any questions related to this job opportunity or would like further information please contact us via careers@arbutus.ie or through filling out the form. #J-18808-Ljbffr
A pharmaceutical innovation center located in Athlone is seeking a Quality Control Analyst to join their dynamic team. This role requires experience with HPLC and a strong understanding of GMP protocols. Candidates should possess excellent analytical skills, effective communication, and a customer-focused mindset. The position offers opportunities for growth, competitive salary based on experience, and a flexible working environment. Interested candidates must be eligible to work in Ireland and can apply via careers@arbutus.ie. #J-18808-Ljbffr
Job Opportunity - Senior Researcher and Analytical Chemist Salary: Competitive / Based On Experience Department: Verbena Laboratory Quality Team Reporting To: Senior QC Analyst Reference: VER_2215 Arbutus Innovation Centre is advertising this position on behalf of Verbena Limited in Athlone, a speciality laboratory, servicing the pharmaceutical industry. This is an exciting opportunity to work in a fast-paced environment with a small, collaborative and dynamic team of innovators and experienced leaders. JOB PURPOSE Verbena Limited is looking to hire a Senior Research and Analytical Chemist to take a leading role in the analysis and characterisation of novel active ingredients and finished product. The role will require you to supervise a small team of QC analysts. You will prioritise, sample, test and release client test requirements, intermediates and finished products. You will ensure that strict timelines are met, in-line with supporting the business needs and requirements. You will support new formulations /finished products stability programmes. ABOUT THE ROLE We are looking for a Senior Analytical Chemist with Industrial Organic Chemistry experience willing to join a pro-active team. We want you to work in our dynamic, ambitious and fast-paced laboratory and to be challenged in ways that bring the very best out of you. In our supportive environment, you will be an indispensable member of the technical team and integral to your role is working with our partners including world-leading biopharmaceutical companies and academic institutions. Our lab capabilities are diverse and innovative. Ideally, you will have a BSc or MSc in Organic Chemistry or Medicinal Chemistry or a related science discipline with strong laboratory skills and at least 2 years experience in an industrial environment, or PhD in a relevant discipline. Relevant skills required include an in-depth understanding of organic chemistry and reactions mechanisms. You will need to show capability in designing experiments, a proven track record of practical research experience with multi-step synthetic chemistry including, purification using automated systems (flash chromatography and preparative HPLC), and analytical characterisation techniques such as column chromatography, LC-MS and GC-MS. As a confident IT user, you will be familiar with MS Office, and specialist software including LIMS systems such as Empower. You will be able to work both independently and as part of a team, have good leadership, planning and organisational skills. In addition, you will have a high level of attention to detail and be able to identify and analyse and resolve routine problems. You will demonstrate an ability to communicate clearly both orally and in writing, keeping team and management informed. Responsibilities Include: Primary Responsibilities Use analytical techniques and instrumentation mainly LC/GC based using Empower 3 software. Develop techniques for the analysis of active substances and chemicals. To draft and contribute to Quality and Controlled documents. Support maintenance of controlled drug procedures. Liaise with controlled drug responsible officer and security providers to ensure quality and safety systems are adhered to. To independently design and carry out routine and complex experiments as necessary. Analyse samples from various phases of client manufacturing processes. Interpret data and meet strict guidelines on documentation when recording data. Report and extrapolate analytical results and data. Work collaboratively in cross-functional teams. Liaise with production personnel to ensure compliance and efficiencies are met. Be aware of, and keep up to date with, health and safety issues. Support batch release processes. Support QA lead in the preparation for and during audit inspections. Support new product introductions. Grant writing and applications. Secondary Responsibilities Validate methods and equipment. Support other activities within the Quality department as assigned by the in-line Senior Manager. Support the generation and approval of Quality Reviews and Annual Product Quality Reviews. Identify continuous improvement and collaboration opportunities, promoting development and implementation of quality data and reports for improvement and optimisation of business processes / results. Light regulatory and compliance tasks. Support existing and develop new relationships with Third Level Institutions and government agencies related to service offerings. Support Internship programs. What We Offer Strong Opportunity for growth Opportunity to learn and grow across departments Flexible working options Additional Information To be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position. Equal Opportunity Employers We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Arbutus Innovation Centre and its client companies are committed to celebrating this, in all its forms. We strive to build a culture that encourages, supports and empowers our employees. Competitive Salary & Benefits: Interested candidates should submit an updated CV and cover letter to: careers@arbutus.ie IRELAND Daneswell Business Park Monksland, Athlone Co. Roscommon Republic of Ireland Contact Us If you have any questions related to this job opportunity or would like further information please contact us via careers@arbutus.ie or through filling out the form. #J-18808-Ljbffr
A leading innovation center in Ireland seeks a Senior Researcher and Analytical Chemist to lead analysis and characterisation of active ingredients. The role requires supervising a team and developing new analytical methods. Candidates should possess a degree in Organic Chemistry or a related field, with industrial experience. The position offers competitive salary and opportunities for growth in a collaborative environment. #J-18808-Ljbffr
