http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/quality-associate-contract-republic-of-ireland-200642716.htmFri, 20 Nov 2009 13:13:06 +0000195730Quality Associate 12 Month Rolling Contract My client is a pharmaceutical company based in Dublin and they are seeking a Pharmaceutical Quality Associate whos remit will be to evaluate the quality aspects of new applications for human medicinal products with the IMB and variations to/renewal of existing market authorisations. Responsibilities: • In conjunction with the QM, local Regulatory Advisor and local Medical Advisor, ensure that the sales and marketing element of the company is compliant with all IPHA, IMB and corporate quality requirements • Update and where necessary write SOPs to act as guidance for the affiliate to ensure that we are compliant to quality guidelines • Devise and implement a process map for all current quality systems in the affiliate and update this as new systems are added • Hold monthly compliance meetings to review status of quality adherence in the affiliate and to identify potential areas for improvement • Carry out audits of quality systems locally are specific intervals to ensure that they are effective and to take corrective action where deviations or failures occur in the quality system (CAPAs) • Train all staff members on relevant areas of quality to their function as outlined in the training manualsMaintains all quality documents and records in an up to date manner • Represents the local affiliate to the IMB and UCB Corporate in conjunction with the GM and QM on all matters relating to quality • Updates and implements elements of the local Risk Management Plan • Liaises with the Pharmacovigilence and Medical Information divisions to ensure that all reports are completed for the affiliate. • Act as a lead on quality matters in the local affiliate and with the GM and QM to set a standard for all staff Experience and Qualifications: - 2+ years previous experience in managing quality systems is essential with preference given to those that have worked in quality management in a sales and marketing unit of a pharmaceutical company. - A degree in science or ideally a higher qualification is essential. ************************************************************** For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 4747 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy *************************************************************** Life Science Recruitment | http://lifescience.ie Life Science Recruitment is Ireland’s foremost specialist scientific and healthcare recruitment agency. We specialize in scientific, pharmaceutical, biotechnology, chemistry, quality management, clinical research, medical, allied healthcare, regulatory affairs, engineering, pharmacy and research jobs in Ireland. Check out our specialist websites now to view our latest jobs – choose your area of interest… lifescience.ie * pharmaceutical.ie * alliedhealth.ie * clinicalresearch.ie * scientificjobs.ie * medicaldevice.ie * biopharmaceutical.ie http://www.newscientistjobs.com/jobs/job/formulation-scientist-republic-of-ireland-200644125.htmFri, 20 Nov 2009 13:10:53 +0000195703Formulation Scientist This is an excellent opportunity to join an innovative R&D facility, based in Dublin, with extensive growth plans for the next few years. This is a key role within the organisation and requires someone who can lead and direct projects on an internal and external basis. Role/Opportunity: • Development of formulations from new to clinical trial batch stage. • Execution of investigational medicinal product batches in compliance to cGMP • Mentoring and training inexperienced formulation scientists in the area of solid dosage development and manufacture • Represent formulation on project teams • Interpreting analytical data related to development and clinical batches • Interaction with Quality on formulation specific issues Skills/Experience: • Minimum education to degree level • At least 5 years experience in a Formulation role • Experience of manufacturing in a cGMP regulated environment • Experience in working in cross functional project teams • Strong interpersonal skills For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 4747 http://www.newscientistjobs.com/jobs/job/quality-and-product-development-executive-republic-of-ireland-200644136.htmThu, 19 Nov 2009 15:16:43 +0000195421Quality and Product Development Executive Responsibilities: •Updating and enforcing the company quality system (to ISO9001 standard) •New product development •Day-to-day management of HACCP system and management of finished product testing •Organisation of logistics for overseas shipments •Potential to take managerial role within the company Required Characteristics: •3-5 years experience in quality, chemistry or microbiology in a production environment. •Degree qualified (Science), preferably in Chemistry •Knowledge of GMP, GHP and GLP. Ability to work on own initiative. •Knowledge of Microsoft Word, Excel, Powerpoint, Outlook. •Full clean drivers licence. •Good medical history. ************************************************************** For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem, on +353 1 685 4747 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy *************************************************************** Life Science Recruitment | http://lifescience.ie http://www.newscientistjobs.com/jobs/job/locum-medical-scientist-biochemistry-republic-of-ireland-200642690.htmWed, 18 Nov 2009 14:18:28 +0000195423Locum Medical Scientist Biochemistry NEW ROLE JUST IN Locum Medical Scientist in Biochemistry for immediate start in busy Hospital laboratory. AMLS membership is essential. Garda clearance on file in the NRF will expedite the process significantly. Experience in a hospital biochemistry laboratory is essential as you will be required to move into the role immediately without training. For immediate consideration please apply online or contact Eamonn O'Raghallaigh on 01-6854848 http://www.newscientistjobs.com/jobs/job/production-supervisor-pharmaceutical-republic-of-ireland-200642322.htmTue, 17 Nov 2009 21:41:31 +0000195390The successful candidate will be responsible for day to day operations in the Production area. This includes responsibility for the management of production resources to achieve the requirements of the production schedule. Reporting to the Business Unit Director, the successful candidate will possess the following key skills: •Strong Leadership/Organisational skills. •Demonstrated ability to lead change and produce innovative solutions to problems •Good influencing skills and the ability to build good working relationships •Track record in delivering results, demonstrating an ability to work through issues rather than around them. •Identification and Implementation of Continuous Improvement initiatives. •The proven ability to identify the skills and strengths of others in delegating responsibilities to achieve strategic goals. Key Responsibilities will include: •Responsibility and accountability for the Production Function/Area •Display leadership and guidance to the production team and promote and implement Schering Plough systems and initiatives. •Enhance the necessary skills of the business unit team to meet their objectives through focused training, development plans and succession planning. •Ensure all production activities are documented as required. •Ensure compliance with SHE, cGMP and other business regulations • Monitor performance to metrics, manage resources and prioritise to achieve targets. •Assist in the development and transfer of new processes. •Prepare budgets and control expenditure to operating plan The ideal candidate will have at least five years supervisory experience preferably in a Sterile Manufacturing environment. They will have the ability to work shift and should have a Microbiology qualification. This position provides excellent career opportunities. The ideal candidate will have the capacity to grow and develop to a Managerial role within a 4 year time frame. ************************************************************** For Immediate Consideration Please Apply Online Now If you would like further information before applying please contact: Eaomonn O’Raghallaigh MSc on +353 1 685 4848 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy *************************************************************** Life Science Recruitment | http://lifescience.ie Life Science Recruitment is Ireland’s foremost specialist scientific and healthcare recruitment agency. We specialize in scientific, pharmaceutical, biotechnology, chemistry, quality management, clinical research, medical, allied healthcare, regulatory affairs, engineering, pharmacy and research jobs in Ireland. http://www.newscientistjobs.com/jobs/job/sr-qa-specialist-biopharma-republic-of-ireland-200642064.htmTue, 17 Nov 2009 15:53:13 +0000195409Sr. QA Specialist - BiopharmA This company is one of the world’s leading biopharmaceutical companies. Through acquisitions and mergers, this company has expanded rapidly in its short history and as a result of this continued growth; a new opportunity within this organisation has arisen for a QA Project Manager. This position is responsible for monitoring and supporting the quality performance of contract manufacturers, distributors, material suppliers to all applicable standards for GMP and GDP. This position is responsible for leading, monitoring and supporting the quality performance of European quality systems according GMP & GDP standards. The individual may be responsible for, but is not limited to: • Reviewing and approving batch documentation, data, COAs and supporting QP functions • Supporting batch disposition • Designing and implementing European quality systems and maintaining quality metrics • Approving and leading deviations, change controls, CAPA, investigations and nonconformance reviews, etc. • Leading drug product complaints and support any recall efforts in conjunction with QP • Conducting external audits independently as lead auditor • Conducting training, including GMP/ GDP, for European staff • Implement Technical Quality Agreements, as required • Support Product Quality Review, as necessary • Participating in technology transfer, process scale-up, and process improvement projects. • Leading meetings with external parties and representing the company in a professional manner Essential: • Bachelor’s degree in chemistry, biology or a related discipline • 5 years plus experience working in Quality Assurance, and/or Qualified Person role to support the manufacturing of drugs, biologics, or devices. • Thorough understanding of quality systems and cGMPs. • Experience conducting audits as lead auditor • Interpersonal skills and professional skills to interact with contractors while representing Shire. • Must be flexible and comfortable in a “start up” environment • Must be able to prioritize and multitask in a stressful environment. • Must be able to travel up to 50% (domestic and international) Desired: • Quality experience in parenteral biotech manufacturing (aseptic or sterile processing) • Experience working with a Qualified Person or Responsible Person • Experience interfacing with regulatory bodies or working on regulatory submissions. ************************************************************** TO APPLY DIRECTLY PLEASE CLICK HERE If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 47 47 http://www.newscientistjobs.com/jobs/job/qa-project-manager-biopharma-republic-of-ireland-200642040.htmTue, 17 Nov 2009 15:43:27 +0000195411QA Project Manager This company is one of the worlds leading biopharmaceutical companies. Through acquistions and mergers, this company has expanded rapidly in its short history and as a result of this conitued growth, a new opportunity within this organisation has arisen for a QA Project Manager. This position is responsible for monitoring and supporting the quality performance of contract manufacturers, distributors, material suppliers to all applicable standards for GMP and GDP. The individual may be responsible for, but is not limited to: Managing priorities and tasks at Contract Manufacturer. Leading and monitoring the daily operations at the Contract Manufacturer. Leading and performing batch review and QA disposition. Designing, Implementing and improving quality systems and metrics. Reviewing and approving; batch records, specifications, deviations, change controls. Leading investigations. Facilitating technology transfer, process scale-up and process improvement projects. Leading meetings of suppliers. Building authentic relationships with Contract Manufacturing. Leading audits. Maintenance of all relevant Technical Quality Agreements (TQAs). Leading Product Complaints and Recall. Leading and assisting in regulatory agency inspections. Supporting the Product Quality Review. Leading training Minimum Bachelor’s degree in pharmacy, chemistry, biology or a related discipline. Extensive experience working in a QA role. Significant experience working in biopharmaceutical industry. Thorough understanding of quality systems, cGMPs, GDPs. Experience with Aseptic/ Sterile Processing. Excellent interpersonal skills and professional skills to interact with contractors while representing the company. Must be flexible and comfortable with ambiguity in a “start up” environment. Must be able to prioritize and multitask in an environment with changing priorities. Must be able to travel up to 50 %. ************************************************************** If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 47 47 Your details will not be passed to a Third Party without your express Prior Consent. http://www.newscientistjobs.com/jobs/job/principal-chemist-suncare-republic-of-ireland-200641966.htmTue, 17 Nov 2009 15:13:27 +0000195405Principal Chemist (Suncare) Reporting to the Skincare NPD Manager, this is a key role within the Formulation and NPD Team Responsibilities - Formulation Own and drive the development of a library of sun protection bases for suncare and skincare ranges across all price bands and complexity to meet future needs. Work collaboratively with the claims testing facility, to develop robust bases for suncare products Ensure all relevant stability, testing and paperwork is available to enable technologies to be able to enter the New Product Development Process with minimal risk. Work closely with suppliers of raw materials and other external technologies to maximise commercial benefit for the company within the area of sun protection. Build a library of bases and technologies to support NPD and future needs ensuring library remains dynamic and appropriate. Lead appropriate collaborations with external agencies and suppliers to ensure the sun protection technology offer is complete and leading edge. Support the development of the overall Cross Category Technology Strategy. Work closely with the Skin delivery team in the Skin Research Institute to understand the performance and constraints of active ingredients especially in relation to sun protection technology Responsibilities - NPD Lead NPD for suncare and sun protection ranges. Work closely with all the skincare teams to exploit and derive commercial benefit from existing technologies. Gather, interpret and apply strategic Technical Insights for the sun protection sector Lead the skincare Innovation and Ideation Process for the Sun protection sector. Requirements Good first Degree in a scientific discipline Extensive knowledge of cosmetic ingredients particularly sunscreens 5-7 yrs experience developing skincare and in particular sun protection products Experience in Project Management Experience gained through formulating complex skincare products ************************************************************* If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 47 47 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy *************************************************************** Life Science Recruitment | http://lifescience.ie http://www.newscientistjobs.com/jobs/job/rd-group-leader-adhesives-republic-of-ireland-200641957.htmTue, 17 Nov 2009 15:07:22 +0000195399R&D Group Leader Responsibilities: *Directs research and development projects in an assigned department in order to meet organization's needs for technology development, new product development, as well as improvement and cost reduction of existing products and processes. *Direct research programs for new product development and product/process improvement of current products. *Develop product constructions and processes, including all experimentation/evaluation and specifications assembly. *Designs & conducts chemical experiments on both lab- and production-scale. * Responsible for complex basic research and/or product development projects. * Designs and specifies production scale processes and conducts validation thereof. *Prepares test samples and conduct tests on chemicals and/or materials as required to support programs. *Develops new tests as necessary to support projects. Analyzes technical data from both experiments and property testing to draw conclusions. Documents project work in lab notebooks, issues reports, and maintains files on projects. Completes any necessary regulatory forms. *Consults with technical director, operating and sales personnel on group priorities and strategy. Active role in setting overall R&D direction & strategy. Participates in business planning process with one or more business as appropriate. Establishes program priorities, objectives and responsibilities for group. Audits activities and communicates progress. Ensures effective communication of R&D program progress for own work and for overall group. *Participates and leads cross-functional product development teams. *Participates and occasionally leads establishment and implementation of R&D policies and procedures. May be responsible for specified lab areas *Interface with customers on new product applications and facilitate patent activity to protect new technology. Networks externally to assure highest level of competence is maintained. *Develops skills and evaluates performance of department personnel. Mentors and influences other Associates. *Proactively contributes to the development and maintenance of a safe work environment for self and associates. *Makes identifiable and substantial contributions to continuous improvement. Performs all duties consistent with established guidelines consistent with ISO-9001 and those elements of GMP deemed necessary to support our business (as outlined in the Quality Manual). Actively complies with and endorses Department and Company objectives. Requirements: *Education - PhD Required *Supervisory Experience of 4-6 years required *BS degree (or higher) in chemistry, chemical engineering, polymer science or materials science and/or significant industrial experience. *Greater than 3 years adhesive formulation, mixing process and coating process experience. *Familiarity with coated adhesive applications. *Demonstrated technology and/or product development capability *Greater than 2 years supervisory experience ************************************************************* If you would like further information before applying please contact: Brian Christensen BA(Mod.)MedChem on +353 1 685 47 47 Your details will not be passed to a Third Party without your express Prior Consent. View our Privacy Policy *************************************************************** Life Science Recruitment | http://lifescience.ie http://www.newscientistjobs.com/jobs/job/marine-functional-foods-principal-investigatoradjunct-professor-republic-of-ireland-200635165.htmTue, 10 Nov 2009 11:49:31 +0000176877The Marine Functional Foods Research Initiative NutraMara) is a recently created programme for marine based functional food development funded by the Marine Institute and the Department of Agriculture, Fisheries and Food (under its Food Institutional Research Measure). NutraMara consists of up to 30 individual scientists/postgraduate students working on the development of marine based functional foods targeting health areas which include food safety, cardiovascular health, immunity and colorectal cancer. The NutraMara initiative will combine expertise from a number of national institutes including Teagasc’s food centres, University Colleges Cork and Dublin, NUI Galway, University of Limerick and University of Ulster. Teagasc, the Agriculture and Food Development Authority, as the co-ordinator of the NutraMara initiative in collaboration with University College Dublin and University College Cork are now seeking to fill the following post: Marine Functional Foods – Principal Investigator/Adjunct Professor (Ref: PROF/MFRC/0309) The indicative duration of these term appointments is 4.5 years subject to contract. Further information including job specifications, qualification requirements, remuneration and an application form for each post can be accessed by clicking the Apply Now button. The closing date for receipt of completed applications is 5.00pm on Friday 27, November 2009. Teagasc is an equal opportunities employer. Canvassing will disqualify. http://www.newscientistjobs.com/jobs/job/marine-natural-products-chemist-programme-director-of-nutramara-republic-of-ireland-200635105.htmTue, 10 Nov 2009 11:37:40 +0000176819The Marine Functional Foods Research Initiative NutraMara) is a recently created programme for marine based functional food development funded by the Marine Institute and the Department of Agriculture, Fisheries and Food (under its Food Institutional Research Measure). NutraMara consists of up to 30 individual scientists/postgraduate students working on the development of marine based functional foods targeting health areas which include food safety, cardiovascular health, immunity and colorectal cancer. The NutraMara initiative will combine expertise from a number of national institutes including Teagasc’s food centres, University Colleges Cork and Dublin, NUI Galway, University of Limerick and University of Ulster. Teagasc, the Agriculture and Food Development Authority, as the co-ordinator of the NutraMara initiative in collaboration with University College Dublin and University College Cork are now seeking to fill the following post: • Marine Natural Products Chemist (Programme Director of NutraMara) Principal Investigator/Adjunct Professor (Ref: PROF/AFRC/0309) Further information including job specifications, qualification requirements, remuneration and an application form for each post can be accessed by clicking the Apply Now button below. The closing date for receipt of completed applications is 5.00pm on Friday 27, November 2009. Teagasc is an equal opportunities employer. Canvassing will disqualify. http://www.newscientistjobs.com/jobs/job/trainee-scientific-sales-professional-ireland-republic-of-ireland-200620518.htmMon, 26 Oct 2009 10:21:11 +0000151559Keywords: - NIR, Food, agriculture, sales, Dublin Our client is seeking a trainee sales professional to maintain and grow their business in Ireland!! Ideally, you will be an exceptional relationship builder with a good understanding of Chemistry and related analytical/wet chemistry techniques. Experience in a commercial environment will be highly beneficial and you must have a willingness to travel extensively.Perfect for a new science graduate with some sales experience. Only apply if you are fully committed, have strong interpersonal and team skills, a proactive mindset and a thirst for success. Contact VRS immediately for more information on this exciting new role!! http://www.newscientistjobs.com/jobs/job/industrial-chemist-north-west-of-ireland-republic-of-ireland-200350399.htmMon, 16 Feb 2009 11:01:52 +00009465 Summary: Our client, a leading healthcare organisation, is currently recruiting an Industrial Chemist for the role of Process Specialist in their Technical Manufacturing group. This role is based in Sligo.  Description: Our client, a leading healthcare organisation, is currently recruiting an Industrial Chemist for the role of Process Specialist to support manufacturing and technical activities in their Technical Manufacturing group. The Technical Manufacturing group in the Scientific Services department is responsible for the manufacture of Microparticle and Conjugate Concentrates that are the active components for diagnostic reagent production. The group also owns and supports the manufacturing processes from a technical perspective. Responsibilities: To ensure the area meets its production schedule targets in the manufacture of Conjugate and Microparticle concentrates. To monitor the performance of the manufacturing processes via tracking of key process parameters and to investigate improvement programs as required. To carry out operations in the manufacturing and testing areas, ensuring that all documentation is complete and compliant. To work in concert with Technical Specialists to identify, document, investigate and remedy the cause of product non-conformance, in compliance with site CA/PA system requirements. To participate in laboratory maintenance programs, for example instrument maintenance and calibrations and ordering of laboratory reagents. To assist in product development/improvement projects. To design and manage process improvement projects and validations. To assist in the deployment of a Business Excellence culture in the area. To identify and implement cost improvement and cycle time reduction opportunities. To build a knowledge base on the manufacturing via process characterization studies. To ensure the smooth transfer of new processes from other sites into the plant, in compliance with regulatory requirements. To lead initiatives for training new employees. To adhere to all GLP and GMP requirements and ensure safety standards are met and safe working practices are adhered to. To ensure that activities are completed within budgeted guidelines. To assist in preparation of the annual departmental budget. Requirements You will have a post-graduate qualification in chemistry or biochemistry with experience in a Process Engineering/Development or similar role. Technical or manufacturing experience in any of the following areas would be an advantage: bioconjugation, microparticle coating, protein purification, chromatographic method, chemical/pharmaceutical processes. Ability to interact effectively with plant personnel including staff at other sites within the division. Evidence of a high standard of personal performance in one’s current position/academic background. Excellent communication and presentation skills are essential prerequisites for this position. For further details please contact Angela on 071 9142411 or email your CV in confidence angela.haran@collinsmcnicholas.ie   This role requires applicants to have a full working visa.  Collins McNicholas Sligo Milbrook House Kennedy Parade Sligo