http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/technical-delivery-manager-md-maryland-200642313.htmFri, 20 Nov 2009 22:00:00 +0000196373My company shares my passion for helping to improve human health around the world. This is My MedImmune. Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Technical Delivery Manager Location: MD, Gaithersburg - Corporate Headquarters Req: 02109 Job Description Position will work in IT addressing the business technology needs within the area of Medical and Regulatory Affairs. Position will be responsible for understanding business problems and working with relationship managers, business analysts and technical teams to develop technology solutions in support of business needs. In addition, position will be responsible for overseeing technology solutions; implementing system-based solutions; and managing vendor partners and internal resources in the delivery and support of technology to satisfy MedImmune's business capability needs. Position will be responsible for technical oversight and management of projects. Position will own technical requirements definition based on functional requirements and taking the solution blueprint, in conjunction with the user requirements, and turning it into a detailed design or configuration. Position will assess the scope of new project efforts by estimating the work involved, resources required and time line for technical delivery efforts. Position owns solution prototyping and change management, blueprinting (fit/gap) and quality assurance; manages the development and delivery activities within SDD in support of project and non-project activities. Has direct responsibility for the overall success of the assigned project and deliverables, either through direct participation or oversight. Projects may include new applications and modules, major or minor enhancements to existing applications or modules and product upgrades. Position will work with business owners, relationship managers and IT to manage the development to production and the production to operations activities following established methodology. Activities include internal code reviews, testing, supporting user acceptance testing, developing a support approach, application training, disaster recovery plans, application process maps and others as defined by the IT PMO. Position will keep customers (to include business owners, relationship managers, and internal IT management) apprised of progress, issues, and risks in a timely manner. Position will practice risk management strategies to ensure that project commitments are realistic and met. Position will participate in the establishment and implementation of SDLC methodologies, ITIL processes and IT PMO processes and ensure that IT projects adhere to those standards and meet customer expectations International travel may be required. Additional requirements for Medical and Regulatory Affairs include: Experience with Medical and Regulatory Affairs in a pharmaceutical or biotech environment. Clinical trials knowledge. Experience with data warehousing and data mining. Skills: Demonstrated ability to manage software development teams, implementation of off the shelf software packages, and interdependencies within an IT development organization. Demonstrated ability to manage cost, schedule, and performance of IT development projects and departments. Demonstrated ability to manage different development resources to include, internal, external, contracted staff augmentation resources, and outsourcing partners. Ability to collaborate and engage IT stakeholders including IT security, Validation/QA, IT Infrastructure, and Enterprise Architecture as needed. Proven ability to identify, manage and mitigate issues and risks. Demonstrated oral and written communication skills. Experience presenting project information in a formal and informal setting. Demonstrated focus on meeting customer expectations and working with a customer service mindset. Demonstrated interpersonal skills with experience managing diverse teams. Demonstrated ability to staff and develop individuals and teams. Demonstrated commitment to staff development and retention. Demonstrated ability to conduct facilitated sessions with end users and business owners in order to define requirements and review project progress. Demonstrated skills in problem identification, isolation and resolution through the use of analysis, troubleshooting and other like techniques. Experience coaching staff on problem resolution techniques Functional Knowledge is necessary in the following areas: Biotech or Pharmaceuticals; Validated Systems Environments; Sarbanes-Oxley Requirements; Data and Application Security; Business Intelligence Processes and Methodology knowledge is necessary in the following areas: Familiarity with ITIL; SDLC processes to include rapid and waterfall development; Project management of multiple development projects; Data Analysis. Experience with electronic publishing processes (e.g. eCTD and other formats), document management (Documentum, LiveLink, etc) is highly desirable. Technical Skills are necessary in the following areas: Application Platforms (SharePoint, SharePoint Portal Server, SharePoint Server 2007, Web Logic, IIS). Application Development (XML, WebServices, Middleware such as BizTalk or BEA Aqua Logic); MS Office Suite of Products; Database and Business Intelligence (Data warehousing, Oracle, TOAD or other similar, SQL Server, MS Access); Development Applications (Visual Studios Team Services, Development management tool such as Rational or visual studio, etc.); Programming Languages (SQL, PL/SQL, Transact-SQL, C#) JOB REQUIREMENTS: Job Requirements Education: Bachelor's degree from accredited college or university is required. Bachelor's or master's degree in computer-related curriculum is desired. Experience: 6+ years of work experience; 4-5+ years of IT work experience, with progressively more responsibility; Proven track record of managing and coordinating several projects simultaneously while delivering on time, on schedule, and meeting customer expectations; Experience project planning from project inception through transition to operational support; 1-2 years in a pharmaceutical, biotech, or consumer goods environment; 2-3 years of managing technical resources to include internal and vendor partners; Ability to provide leadership, management and technical expertise to a culturally diverse, technically-oriented staff If you are interested in this position please click the Apply Now button below and search for Req #. 02109. MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/formulation-scientist-225337-nj-new-jersey-200645875.htmFri, 20 Nov 2009 20:59:35 +0000196366A leader in therapeutic antibodies, ImClone Systems is committed to advancing oncology care by developing a portfolio of novel targeted biologic treatments designed to address the medical needs of patients with a variety of cancers. Founded 25 years ago, ImClone Systems has a rich culture of biotechnology innovation and leading-edge medical science. Our deep expertise in molecular biology, oncology, genomics and antibody engineering has helped us establish a robust pipeline of products that are in various stages of clinical development and span virtually all major solid tumor types. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. Assists in the development of formulations for protein therapeutics. 2. Operation of analytical instrumentation including: HPLC, Electrophoresis (SDS-PAGE and IEF), Spectrophotometer, CD, Fluorimeter, DSC, FTIR, HIAC, DLS, pH meter, Conductivity Meter, Osmometer and Freeze Dryer. 3. Execute experiments, analyze data, and report results to supervisor within timelines. 4. Active participation with supervisor in planning and executing experiments. 5. Write SOP’s, study protocols and technical reports. 6. Sample management and monitoring of stability samples. 7. Assay development and trouble shooting. 8. Assist in the development of final drug dosage forms. 9. Maintain Laboratory and Laboratory Records. 10. Work in a safe manor compliant to ImClone Systems policies and procedures. ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE 1. BS in Biochemistry/Pharmaceutical Science with 8-12 years of relevant industry experience or MS in Biochemistry/Pharmaceutical Science with 4-8 years of relevant industry experience. 2. Knowledge of the use of and experience with Spectrophotometer, CD, Fluorimeter, DSC and HPLC is preferable. 3. Must have good written and oral communication skills. 4. Must have good organization and documentation skills. 5. Must have the ability to accurately prepare solutions, perform experiments and analyze data. 6. Must be detail orientated and have demonstrated time management skills. To apply please visit http://www.imclone.com/careers_imclone.php,Requisition #225337. http://www.newscientistjobs.com/jobs/job/associate-scientist-iiscientist-i-md-maryland-200645868.htmFri, 20 Nov 2009 19:16:57 +0000196350My company shares my passion for helping to improve human health around the world.” “This is My MedImmune.” Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc. Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world. Title: Associate Scientist II/Scientist I Location: CA, Mountain View - NON SALES Req: 02056 Position Summary: Major Duties and Responsibilities (including supervising others): We are seeking a highly motivated independent individual to join our formulation team aimed at formulation development for biologics including protein and live viruses. The individual will be working with the team focusing on formulation studies and characterizations for liquid or solid dosage formulations. The essential responsibilities will include planning and executing pre-formulation and formulation studies, developing and performing biophysical, biochemical and biological analyses. An ability to work independently and have effective organization and communication skills is essential. Special Skills/Abilities: Expertise in pre-formulation and formulation of proteins and antibodies required. Hands on expertise in analytical techniques including HPLC-SEC, RP-HPLC, FTIR, fluorescence assays, DSC/mDSC are required. A prior experience in ajuvant formulation development is a plus. Experiences with solid state analyses such as Karl-Fischer, TGA, DVS, particle sizing desired. Excellent oral and written skills required. Job Complexity: Medium-High. JOB REQUIREMENTS: Supervision: Work is performed with minimal supervision. (supervision required, level of independence) Requirements/Qualifications: Education: Degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biophysics. Experience: Ph.D. + 0-3 yrs, M.S. + 8-10 yrs, B.S. + 10-13 yrs. If you are interested in this position please click the Apply Now button below. Req #. 02005 MedImmune is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, or any other characteristic protected by federal, state or local law. http://www.newscientistjobs.com/jobs/job/technical-manager-runcorn-200645711.htmFri, 20 Nov 2009 16:47:45 +0000196053Our clients tablet manufacturing plant in the North West has generated significant profit growth over the last 5 years and has ambitious plans for future growth. It currently employs 135 staff and has a turnover of £15M. As a member of the senior management team this role reports to the Managing Director and through functional managers assumes responsibility for product development, quality control and quality assurance Vacancy 1 Manage the introduction and registration of products under the Traditional Herbal Medicinal Products Directive. 2 Keep abreast of and advise on marketplace trends and legislation in order to identify new product opportunities. 3 Provide solid and commercially sound technical advice to the Sales function. 4 Provide operations support in respect of formulation and process development. 5 Manage the QA/QC functions Candidate The candidate will: Be a science graduate currently operating in the food supplements, healthcare or food industry in a product development, formulation development or regulatory role. Have an understanding of the legislative framework within which we operate. Have a keen interest in new product concepts and formulation development. Be commercially and financially aware, with the skills to bridge the gap between the technical and commercial functions. Be bright and articulate and adept at building strong personal relationships and have the presence to be a credible member of the Company's senior team. Have worked in or managed a quality control function including experience of method development Please Apply Now! The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. Carlisle Staffing plc, trading as SRG is an Employment Business/Agency. SRG winners of the 2008 Recruiter Awards for Excellence: Best Candidate Care and Best Health Care/Medical Recruitment Firm. http://www.newscientistjobs.com/jobs/job/assistant-technologist-east-anglia-east-anglia-200645688.htmFri, 20 Nov 2009 16:36:49 +0000196015Our client is seeking an Assistant Technologist, within their inhalation toxicology group. The successful candidate will have a HND or BSc in Chemistry/Biochemistry or related discipline with some experience in inhalation toxicology. The candidates will have: Excellent organisational, multi-tasking and problem solving skills Able to prioritise and manage workloads to the required deadlines. Enthusiastic and motivated Excellent written, oral and communication skills. To apply for this position, candidates must be eligible to live and work in the UK http://www.newscientistjobs.com/jobs/job/postdoctoral-positions-with-interest-in-protein-structure-function-high-ca-california-200633780.htmFri, 20 Nov 2009 16:29:31 +0000195920Postdoctoral position(s) are immediately available for candidates with interest in protein structure-function, high density lipoproteins (HDL), or lipid metabolism. The focus of our group is on HDL, namely HDL metabolism and the structure -function of HDL's main protein component, apolipoprotein A-I. We are leaders in the field of apolipoprotein structure-function, utilizing this understanding to describe the role of HDL in the prevention of atherosclerosis and towards the improvement of hydrophobic drug delivery. Projects include examination of cellular and physiological processes that govern HDL biogenesis, characterization of genes involved in HDL formation and cholesterol mobilization, analysis of apolipoprotein structure, functional analysis of structural features of apolipoproteins, and investigation into the effect of incorporation of hydrophobic drugs onto HDL. Experience in cell biology, protein chemistry and/or lipid metabolism is encouraged. Position qualifications: The candidate should have completed a PhD, MD or PhD/MD and be available to relocate to the SF Bay Area. Emphasis will be placed on candidates with a background in protein chemistry, genetic analysis, RNA knockdown, o fluorescence microscopy. Furthermore, those with history of team-work and group coordination will be prioritized. PHYSICAL REQUIREMENTS: Sit: Up to 8 hours/day Stand/Walk: Up to 6 hours/day Bend/Stoop: Up to 6 hours/day Reach: Up to 6 hours Rep Use of UE/Grasp: Up to 8 hrs Lift/Push/Pull: 25lbs, over 25# with assistance or equipment This job requires the ability to hear alarms clients and/or instruction. The ability to see accurately from 20 inches to 20-ft. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential function of this position. TO APPLY CLICK APPLY NOW BELOW AND REFERENCE POSITION 5262 http://www.newscientistjobs.com/jobs/job/product-development-chemist-materials-cambridge-25-30k-cambridgeshire-200645435.htmFri, 20 Nov 2009 15:19:44 +0000195508Product Development Chemist - Materials / Polymer sector - Cambridgeshire - £25 - £30k We are looking for a candidate with proven experience in polymer / material science and product development to join a multinational organisation that is the number one producer of composite materials. Based at their facility in Cambridgeshire, this role will support the growth of their global wind energy business. The Research and Technology Wind Energy Team has responsibility for developing advanced composite materials and technologies using novel methods and approaches for the Wind Energy industry. The main areas of responsibility for this position surround the design and development of new products and processes for Wind Energy application. This will involve product formulation and development leading to product scale up in the manufacturing sites across the company. You will also be required to provide support to Wind Energy customers on new development, formulations and products. This will be an exciting role working on both a local and international level as the wind energy industry grows and expands its use of composite materials. Due to the nature of the job role and business it is essential that you have an innovative approach to science, chemistry and product formulation. In addition to a practical outlook and strong practical laboratory skills you will have the following: - BSc and ideally a Masters degree, PhD or equivalent in Chemistry / Polymer Chemistry - Experience of material science and the advanced composite industry - Proven experience in polymer chemistry, product development and formulation - Experience in the scale up of products into the manufacturing arena - Ideally you will have worked on cross functional global project teams - Strong written and verbal communication skills Salary - £25 - £30k in line with experience plus an excellent benefits package including bonus scheme. http://www.newscientistjobs.com/jobs/job/gc-ms-applications-specialist-south-wales-cardiff-200645348.htmFri, 20 Nov 2009 14:14:19 +0000195253Key words: GC, GCMS, Time-of-Flight, Applications Development Fantastic opportunity for an Applications Chemist with a GC and GCMS background. This position involves leadership of GCMS method development testing in new and existing application areas. Experience of Agilent GC/GC-MS systems is highly preferable. Applicant should be proficient in customer demonstration and training and also have experience working in a customer-facing environment. Candidates must be based in South Wales and expect to travel occasionally to customer sites.Contact VRS immediately for more information on this exciting new position. Key words: GC, GCMS, Time-of-Flight, Applications Development http://www.newscientistjobs.com/jobs/job/inhalation-scientist-south-east-200645331.htmFri, 20 Nov 2009 14:03:30 +0000195209INHALATION SCIENTIST - 6 MONTH CONTRACT - KENT NES UK are recruiting for an Inlalation Scientist for our global pharmaceutical client based in Kent. The role will need experience of analysis of inhaled products. You will need to have experience of analytical techniques including HPLC and GC. You must also be experienced in working to GLP. This is a 6 month contract with the possibility of being extended. Please apply to Geoff Flavell-Matts at NES. http://www.newscientistjobs.com/jobs/job/principal-research-scientistteam-leader-south-east-london-200645305.htmFri, 20 Nov 2009 13:46:06 +0000195141Unique opportunity for an accomplished analytical chemist! This is a challenging position managing a large number of small molecule analytical studies. Handling up to 50 GLP studies at any one time, you must possess exemplary organisation and study planning skills. You will be responsible for a team of analysts ensuring that studies come in on time and within budget. As technical leader you must have a strong analytical chemistry background, experienced with a range of techniques including HPLC, LC-MS/MS, GC and GC-MS. Superb communication skills are essential, as is previous staff and study management experience. Contact VRS for further details!! http://www.newscientistjobs.com/jobs/job/quality-associate-contract-republic-of-ireland-200642716.htmFri, 20 Nov 2009 13:13:06 +0000194657Quality 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 +0000194630Formulation 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/inhalation-analyst-united-kingdom-200644786.htmFri, 20 Nov 2009 11:16:04 +0000194304We are urgently seeking Analytical Scientists with inhalation experience for a world leading pharmaceutical company. Candidates will be responsible for pharmaceutical analysis using analytical techniques for inhalation product testing using supporting technologies as appropriate. Some stability investigations may also be involved. Experience of the following is required: - inhalation product testing - modern analytical techniques, especially HPLC - GLP and GMP - developing analytical methods This is a 6 month temporary position. To apply for this position, candidates must be eligible to live and work in the UK. Matchtech Group Plc is acting as an Employment Business in relation to this vacancy. http://www.newscientistjobs.com/jobs/job/chemist-yorkshire-200644755.htmFri, 20 Nov 2009 10:53:16 +0000194217Chemist - Personal Care Products Ref: 16025 Great opportunity for a versatile, development chemist to join an interesting organisation that manufactures personal care / healthcare products. Based in East Yorkshire, the successful candidate would be involved with: - Formulating client products to match specifications; - Assisting with scale-up to pilot plant; - Transfer to final manufacture processes; - Trouble-shooting as and when necessary; - Liaising with internal teams to ensure that all work is carried out to Quality guidelines and Health and Safety standards Applications are invited from candidates with a BSc / MSc /PhD in Chemistry or related subject together with a 'hands-on approach' and previous formulation experience. In addition previous GMP experience would be advantageous. This is a permanent position, offering a salary of up to £23,000 (depending on skills and abilities). Role: Permanent Salary: Up to £23,000 pa Location: East Yorkshire For further Science Jobs visit www.sci-search.com http://www.newscientistjobs.com/jobs/job/technical-director-north-west-200644690.htmFri, 20 Nov 2009 09:55:19 +0000194114Leading contact manufacturer of Health and Beauty Products in Europe. As a member of the senior management team, this role reports to the Managing Director and through functional managers assumes responsibility for product development, quality control and quality assurance. Responsibilities include: - Manage the introduction and registration of products - Keep abreast of and advise on marketplace trends and legislation in order to identify new product opportunities - Provide solid and commercially sound technical advice to the Sales function - Provide operations support in respect of formulation and process development - manage the QA/QV functions The candidate will: - Ideally have a degree and be currently operating in the food supplements, health care or food industry in a product development, formulation development or regulatory role. - Have an understanding of the legislative framework - Have a keen interest in new product concepts and formulation development - Be commercially and financially aware, with the skills to bridge the gap between the technical and commercial functions - Have worked in or managed a quality control function including experience of method development Reed Specialist Recruitment Limited is an employment agency and employment business. http://www.newscientistjobs.com/jobs/job/team-leader-mlv-pharmaceutical-company-denmark-200641399.htmFri, 20 Nov 2009 09:53:47 +0000194102Team Leader - Måløv - Pharmaceutical company This is your chance to join the world leader in diabetes care and put your personal mark on R&D projects with the powerful potential to lift the quality of life for millions of people around the world. With the creation of the Oral Protein Formulation Unit (OPF), Novo Nordisk is starting its voyage towards the development of Solid Dosage Forms of diabetes proteins for oral delivery. Our ambition is to develop break-through products with orally available versions of insulin and GLP-1. You will be involved in CMC activities for development within protein formulations for oral delivery, covering formulation, process technologies and development, and pharmaceutical-technical tests. Challenges As Team Leader, you will be the focal point for your team. Coaching, set directions and motivating a team of 15 formulation principal scientists, scientists and technicians – as a leader and an expert in solid dosage forms – you will drive the work forward and ensure that your team meet the set goals. Also, you ensure the personal and professional development of the team as a whole as well as the individual team members. You combine your skills as a leader and your knowledge of Solid Dosage Forms. Your overall goal is to contribute to enabling Novo Nordisk quickly to enter clinical trials with our new oral protein formulation concepts. This position is unique as it allows you to work in a field that combines oral Solid Dosage Forms with proteins and peptides. You will be central in the pharmaceutical development and you can look forward to becoming a key part of our international R&D organisation. You will find an abundance of professional and personal development opportunities in this position, additionally you can look forward to collaborating with experts from different fields in an international environment. Qualifications Most importantly, you are an experienced manager and have already proven your excellent leadership skills and your ability to coach and motivate a team. You hold a Master’s degree or a PhD in Pharmacy, Engineering or another relevant scientific discipline and have some years of experience with the formulation of Solid Dosage Forms, process optimisation, mixing, granulation, compression, coating and capsulation as well as pharmaceutical-technical analyses. As you will be working with colleagues from different fields and of different nationalities, it is essential that you have strong communication skills and thrive in an environment where international teamwork is key. In return, we offer you a world of opportunities starting with influencing the lives of millions of people with diabetes worldwide. http://www.newscientistjobs.com/jobs/job/quality-account-manager-west-yorkshire-200644682.htmFri, 20 Nov 2009 09:49:57 +0000194104This Food company have a natural passion for new technology plays a vital part in how they strive to grow their business and bring consumers closer to nature. As the energy of business, they combine a technical, engineering mindset with quality orientation and desire to head their continuous evolution. They are currently looking for a Quality Account Manager to join their technical team. Key Responsibilities are: - Ensuring that the brand and customer product specifications are completed accurately, approved and issued in a timely manner. - Assess legal compliance of artwork and advertisement materials - To conduct supplier assurance audits to ensure that the companies and customer quality standards and codes of practice are met - To ensure that all non-conformance raised in customer audits are recorded, agreed, followed up and closed out to a satisfactory conclusion - To ensure customer technical queries and problems are answered and resolved to enable a permanent and satisfactory conclusion - To prepare and update the supplier assurance audit schedule - Liaise with Global Purchasing to ensure ingredient and packaging supplier information is complete and adequate to fulfil customer and BRC requirements Candidates must be able to demonstrate experience working in a technical role at managerial level within diary or food related industry either in Operations, Quality or Engineering disciplines. - Must have a sound knowledge of food manufacturing, processing techniques and auditing - Knowledge of Quality Management Systems, laboratory methods and GMP Candidates will ideally be educated to degree level in Food Science or a related discipline, have experience of Food Legislation and Retailer Specification Systems. Reed Specialist Recruitment Limited is an employment agency and employment business. http://www.newscientistjobs.com/jobs/job/analytical-chemist-east-midlands-200644669.htmFri, 20 Nov 2009 09:43:46 +0000194089Wilson, Near East Midlands Airport Eurofins Agroscience Services is owned by Eurofins Scientific and is a leading provider of scientific research services, product development consultancy and technical support to the crop protection industry. Our technical activities involve conducting field and laboratory studies on/in agricultural crops to determine the safety and efficacy of new agrochemicals and crop varieties. We are currently looking to recruit an Analytical Chemist to work within our team. Ideally the successful candidate will demonstrate: • A strong academic background in analytical chemistry to at least Degree level • Hands-on experience of analysis of pesticide residues in a GLP environment, using a variety of extraction, purification and concentration techniques • Familiarity in use of quantitation equipment, including GC, GC-MS, HPLC and LC-MS/MS would be advantageous • A methodical, patient and logical approach to work with an aptitude for detail • A high level of initiative and motivation as well as being an enthusiastic team player • The flexibility, dedication and good humour necessary to thrive in a multi-disciplinary, commercially focused environment In return, Eurofins Agroscience Services offers a competitive remuneration package plus the opportunity to work in an ambitious business located in an attractive rural environment. If you feel you are the person we are looking for, please send your CV and a covering letter (including remuneration details) by e-mail or post to Angela Taylor by clicking the Apply Now button or writing to the address listed within the 'View Contact Details' section below. Closing date for applications: 11th December 2009 http://www.newscientistjobs.com/jobs/job/quality-and-product-development-executive-republic-of-ireland-200644136.htmThu, 19 Nov 2009 15:16:43 +0000194348Quality 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/nir-analyst-in-process-testing-east-midlands-200644134.htmThu, 19 Nov 2009 15:13:50 +0000192645NES UK are recruiting for In Process Testing Analyst for their In Process Analytical Team. You will need to have previous experience of NIR and be able to develop methods with NIR. You will ideally have worked within the pharmaceutical industry however we may consider candidates from other backbrounds provided you have detailed experience of NIR. You will also need to have experience within a GMP environment. Please apply to Geoff Flavell-Matts at NES now.