http://www.newscientistjobs.com/jobsNew Scientist Jobshttp://www.newscientistjobs.com/jobs/job/formulation-scientist-225337-nj-new-jersey-200645875.htmFri, 20 Nov 2009 20:59:35 +0000197439A 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/technical-manager-runcorn-200645711.htmFri, 20 Nov 2009 16:47:45 +0000197126Our 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/inhalation-scientist-south-east-200645331.htmFri, 20 Nov 2009 14:03:30 +0000196282INHALATION 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/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/team-leader-mlv-pharmaceutical-company-denmark-200641399.htmFri, 20 Nov 2009 09:53:47 +0000195175Team 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/lead-pharmacist-east-sussex-200643975.htmThu, 19 Nov 2009 13:17:33 +0000193470We are currently looking for a registered Lead Pharmacist to work for a leading private healthcare provider based in Sussex To provide a clinical pharmacist service within the hospital to ensure the safe and effective use of medicines in the hospital, ie * Perform clinical checks on all prescriptions within remit of role, prior to dispensing * Provide a dispensing and clinical advisory service in relation to pharmaceutical products to hospital staff and patients * Ward-based clinical pharmacist service in a specialised area * Manage the ordering, receipt, issuing and destruction of all controlled drugs and hazardous chemotherapy regimes * Ensure compliance with all legislative requirements and Hospital medicine management policies, procedures and protocols and take corrective action where necessary * Ensure appropriate action is taken in response to drug alerts * Ensure the security of all pharmaceutical products To review, develop, update and implement local policies, procedures and protocols for area of responsibility, in accordance with statutory and Hospital guidelines, policies and procedures, etc To contribute to the hospital integrated governance committee To deliver specialist training to clinical staff within the hospital To support the delivery of targets on stock levels, profits and budgets to ensure these are met. To monitor compliance of pharmacy related procedures within the hospital to ensure these are being adhered to and take corrective action where necessary. To participate in cross department audits To supervise and induct Resident Medical Officers and pre-registration students To represent the department at meetings both internally and externally Additional Responsibilities To act as an assessor for a specified area of responsibility. â?¢ To ensure that learners understand what is expected of them, what is to be assessed and how it is to be assessed â?¢ To ensure that the conditions and materials required for assessment are available â?¢ To make the initial judgement of a candidates performance against defined standards, through observation, questioning and product evaluation. â?¢ To support learners in gathering and providing evidence. â?¢ To authenticate the evidence learners provide and ensure all achievement is correctly recorded. â?¢ To identify gaps or shortfalls in learner. To apply for this position, candidates must be eligible to live and work in the UK Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy. http://www.newscientistjobs.com/jobs/job/cta-clinical-trial-administratorclinical-trial-assistant-buckinghamshire-200642368.htmWed, 18 Nov 2009 09:09:48 +0000190325Clinical Trials Assistant/ Clinical Trials Administrator A very good opportunity has arisen for a CTA to join a reputable pharmaceutical company in the UK. The ideal Candidate must be able to demonstrate that they can fulfil the responsibilities and competencies listed below Tasks and responsibilities * Prepare and maintain accurate and up to date in-house trial related files (CAF) according to relevant SOPs and local regulatory requirements * Maintain and develop relevant tracking systems for trial related activities * Maintain and develop study related e-room * Know and adhere to company SOPs, ICH GCP and other regulatory requirements as applicable. * Liaise and communicate with study teams at all levels * Liaise and communicate with external providers * Prioritise workload to ensure tasks completed in timely manner * Any other tasks as delegated by the Global Trial Manager Desirable competencies * At least 2 years experience in the pharmaceutical or healthcare industry preferably within the clinical research environment * Up to date knowledge of ICH GCP guidelines * Excellent administrative and organisational skills * IT literacy - Microsoft Office plus ability to quickly familiarise with, and use, range of computer based systems (e.g. Beacons, CTMS), * Team working - proactive contribution to, and support of, Global Trial Team at all levels * To be able to work independently within area of responsibility * Ability to respond rapidly to changing requirements and environment * Ability to manage workloads and prioritise tasks * Ability to communicate effectively in a multinational environment in a variety of countries - both written and orally To apply send your CV to J.shadare@proclinical.co.uk or for more information please call Janet Shadare on 0207 440 0636 http://www.newscientistjobs.com/jobs/job/team-manager-analytical-chemistry-materials-south-south-east-200639729.htmWed, 18 Nov 2009 09:06:11 +0000190302Team Manager (Analytical Chemistry/ Materials) c£25-30k South Ref: AF/015134 An experienced Team Manager in analytical chemistry (HPLC, LC/MS) with excellent people management skills is urgently required to manage an analytical team who provide a reliable testing service within R&D for a key organisation. As an analytical team manager will be responsible the management for a team who are preparing and analysing test samples using a variety of complex testing instrumentation (HPLC, GC, LC/MS/MS, ICP, GC-MS etc). You will have excellent problem solving skills to develop solutions and provide advice by applying your expertise to solve routine, non routine or novel analytical problems or challenges. Key Responsibilities • Uphold and carry out standard tests undertaken within the Materials Analysis team where there are well established and understood test methodologies. • Support the demands of the laboratory for high volume (all development products will require routine tests) and quick turnaround to produce accurate and timely results for the test requests submitted. • Develop weekly /daily activity (including testing, training, calibration, etc.) plans for team, ensuring that all appropriate options have been considered to meet customer requirements. • Implement talent management strategies to enhance the Team’s skill and flexibility to include: a) performance monitoring; b) multi-skilling; c) ‘specialist’ skills development; and seek opportunities to improve their effectiveness. • Ensure that all daily work routines are conducted in a safe manner, following defined test methods and ISO17025 protocols. Skills/ Qualifications/ Experience - Degree/ MSc/ PhD in Analytical Chemistry/ Materials background - Experience in a variety of complex instrumentation techniques HPLC, LCMSMS, GC, GC-MS, ICP etc - Relevant technical experience resulting in a thorough understanding of supervision in a high volume/quick turnaround ‘routine’ laboratory environment (ISO 17025) - Proven team management / supervisory experience to support and motivate a team in high demand situations. - Ability to understand principles of test processes/methods - Working knowledge of IT applications (Lotus Notes, Word, Excel, etc.) To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015134, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk Due to a high volume of applicants only shortlisted candidates will be contacted. If you are not contacted within seven days of submitting your CV please assume that your application will not be taken further. If you wish to receive feedback to obtain why your application was unsuccessful please use the contact details provided on the advert. 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/pharmaceutical-analyst-nir-specialist-east-midlands-east-midlands-200639246.htmFri, 13 Nov 2009 13:29:53 +0000183166Pharmaceutical Analyst - NIR Specialist - East Midlands My client is looking for a new addition to their In-Process analytical team. The successful candidate will be running NIR analysis and working on method development and validation with a range of raw materials and finished products. Candidates must have previous experience of NIR analysis within a GMP environment. Candidates must also be able to demonstrate previous knowledge of method development with NIR, ideally within the pharmaceutical industry. If you are interested in this role, and match the specifications above, please apply online or contact Dannielle Robbins on 0161 839 2400 (quoting reference P1250DR) for more information. http://www.newscientistjobs.com/jobs/job/senior-scientist-lc-ms-reading-200638429.htmThu, 12 Nov 2009 15:18:47 +0000181520LC-MS Senior Scientist £30,000 - £35,000 + Bonus+ Excellent Benefits Reading RSSL is an independent global leader at the forefront of scientific analysis, consultancy, product development and training, serving the pharmaceutical, healthcare and biopharmaceutical industries. You will contribute to the pharmaceutical business through leading and growing the LC-MS area by application of your expert knowledge to investigative projects and optimisation of existing methodology whilst working to GMP quality standards. Essential Pre-Requisites: Postgraduate degree or degree with extensive experience including expert knowledge of HPLC and LC-MS method development and validation within the pharmaceutical, healthcare or food industries. Experience in managing scientific staff with the ability to effectively coach and delegate to junior staff. Ability to design experiments, trouble-shoot relevant equipment and project manage contracts. Capable of dealing with client enquires, producing accurate quotations and ensuring that the clients expectations are achieved by understanding their specific needs. Expert in data review and interpretation. If you have the qualifications, experience and drive for this role then please submit your updated CV. 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/new-product-focus-editor-pharmaceutical-drugs-pharma-south-south-east-200632918.htmFri, 06 Nov 2009 11:59:17 +0000171941New Product Focus Editor (Pharmaceutical Drugs) £15 an hour South Ref: AF/015110 6 month contract (initially) Our client a key pharmaceutical services provider is actively seeking someone with a background in pharmacy/ medicine / pharmacovigilance /drugs safety/ medical information or pharmaceutical drugs editing to join a growing department with a worldwide industry leader. Key Responsibilities of the Role: • Analysing information received from the company’s offices about pharmaceutical and pharmacological principles of drugs launched worldwide, including drug classification, indication, dosage form and strength. • Creating a record of all new drugs launched worldwide using in-house data, various reference materials such as, Micromedex, Martindale and the Internet. • Proof reading and QA checking of all entries on the database for the monthly production of the LifeCycle New Product Focus CD. The information is disseminated to clients via CD, Internet subscription and via third party online hosts. • Providing information to clients and answering queries on the worldwide availability of newly launched products as well as the pharmaceutical companies responsible for manufacturing the drugs. • Liaising with other departments in the company to identify launches of new chemical entities (NCEs), ensuring this corresponds with information available from outside sources and that these launches are published in a timely fashion. • Informing the R&D team when an existing drug has been launched with a different indication for which it was first approved. Qualifications, Skills and Experience: Pharmacy degree/Relevant Drugs background Pharmacists, doctors, nurses, pharmacy technicians or anyone with good understanding of medical products. It is vital that the person speaks and writes fluently; knowledge of other languages would be nice to have but not essential. Knowledge of recent or new drug launches In depth knowledge of pharmaceutical trade names and generic names drug knowledge, as well as general indications, methods of administration and actions Computer literate Experienced in conduction internet searches Neat handwriting and attention to detail are also essential To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015110, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk http://www.newscientistjobs.com/jobs/job/senior-qc-analyst-pharmaceutical-chemistry-east-anglia-south-east-200631834.htmThu, 05 Nov 2009 11:05:36 +0000169457Senior QC Analyst (Pharmaceutical/Chemistry) c£28-30k East Anglia Ref: AF/015107 An exciting opportunity has arisen for an experienced Senior QC Analytical Chemist with supervisory experience and a good working knowledge of GLP/GMP, gained from working in a pharmaceutical environment, to join an, established Pharmaceutical company. Key Responsibilities The successful QC pharmaceutical chemist will be responsible for setting up a new QC facility on site and building, over time, a small team of analysts responsible for conducting routine analysis of raw materials and bulk products in accordance with current Pharmacopoeial standards. There is the potential for further progression within this role as the facility develops to incorporate finished product testing. Skills/ Qualifications/ Experience Degree in Chemistry, or appropriate scientific discipline. Commercial Pharmaceutical background Knowledge of GLP/GMP Must have commercial practical experience of analytical techniques including wet chemistry, GC, HPLC and a good understanding of the requirements of technology transfer. Good communication skills and computer literacy are essential. Benefits include: 25 days annual leave Annual discretionary bonus Company pension scheme Private Health Care Scheme Post to start Jan 2010 To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015107, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk Due to a high volume of applicants only shortlisted candidates will be contacted. If you are not contacted within seven days of submitting your CV please assume that your application will not be taken further. If you wish to receive feedback to obtain why your application was unsuccessful please use the contact details provided on the advert. http://www.newscientistjobs.com/jobs/job/quality-assurance-officer-runcorn-200631257.htmWed, 04 Nov 2009 18:07:52 +0000168241Do you have a background in pharmaceutical Quality Assurance? Do you have experience in validation? Do you have experience with LIMS implementation (reviewing/approval of validation documentation)? Do you have experience with qualification of packaging equipment validation. Do you have experience with qualification of cleanroom builds and aseptic manufacturing equipment qualification. Do you have understanding of Annex 1, Annex 15, cGMP and 21 CFR Part 11, GAMP? If you can answer yes to all of these questions then I have an excellent opportunity for you! 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/project-scientist-engineer-chemist-south-east-south-east-200630798.htmWed, 04 Nov 2009 17:07:38 +0000168159Project Scientist (Engineer/ Chemist) c£18-20k South East Ref: AF/015101 A fantastic opportunity has arisen for a project scientist engineering or chemistry to be involved in the development, assembly and supply of versatile specialised computer controlled systems in the chemistry field. Candidates will be required to manage a range of projects involving miniature to bench-scale chemical instrumentation/ products, including supervision, testing and on site assembly (worldwide). You will need to liaise with clients, sales engineers and software/electronics specialists in order build, then personally undertake chemical and performance testing, first at our laboratory and then assist after installation at the client’s site. Skills/ Qualifications/ Experience Science (chemistry) / engineering graduates or those with some commercial experience. Well organised, confident and a good communicator, willing to travel and capable of handling multiple tasks at the same time. Some experience in industry will be valuable, especially in an R&D laboratory, Complete confidence in working with computers is essential. To Apply If you would like to be considered for this role, please contact Alison Fisher at Hudson Shribman Scientific Recruitment, quoting reference AF/015101, outlining your particular skills and experience and their relevance to this post. Please call on 020 7421 5200, or reply via email, entering the job title and reference code in the subject field to alison.fisher@hs-scientific.co.uk For up to date career opportunities please visit www.hs-scientific.co.uk Due to a high volume of applicants only shortlisted candidates will be contacted. If you are not contacted within seven days of submitting your CV please assume that your application will not be taken further. If you wish to receive feedback to obtain why your application was unsuccessful please use the contact details provided on the advert. http://www.newscientistjobs.com/jobs/job/stability-co-ordinator-runcorn-200629564.htmTue, 03 Nov 2009 18:12:08 +0000166243A global leader in the manufacture of generic pharmaceuticals is looking to recruit a Stability Programme Co-ordinator for the North West Manufacturing site. The main purpose of this position is to be responsible for managing the QC Chemistry stability programme, to supply quality stability data to support commercial manufacture of existing products on time, in full to the expected standard, to comply with global regulatory requirements and to review and approve analytical documents. Key Results Area: Compliance: to provide specialist knowledge to support the generation of quality stability data in compliance with cGLP, cGMP, Health & safety, SOPs and environmental and regulatory requirements. Customer service: To deliver customer service by testing stability samples in an efficient and timely manner. To test components/raw materials/bulk, and finished product as required through flexible working. Documentation: To complete all QC batch documentation, right first time, i.e. correct and in full, in order to achieve customer service and GMP Provide training and guidance to other members of the department. Lead laboratory investigations in accordance with company procedure. Interpretation and implementation of technical protocols to facilitate method transfer activities Qualifications/Experience: Pharmaceutical experience with relevant science qualification, minimum HND. Knowledge of pharmaceutical stability programme management cGMP/ cGLP Regulatory bodies/ customer requirements Laboratory Analytical Techniques 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/cmc-project-manager-1-year-contract-london-200628894.htmTue, 03 Nov 2009 10:56:23 +0000165733CMC Project Manager 1 Year Contract Our client is a pharmaceutical development and manufacturing company. They currently have an opportunity for a CMC project manager. Reporting to the VP of CMC and Process Science you will support all outsourced CMC activities, ensuring security and supply to support clinical and commercial products as required. You will:- • Ensure security of supply to support clinical and commercial requirements from raw materials through to QP release and supply of product, in line with all relevant guidelines (GMP, GLP, GCP), from a fully outsourced supply chain • Manage the negotiation, contracting and management of outsourced CMC activities, ensuring maximum productivity in terms of quality and cost • Lead and manage outsourced services to ensure best performance and business relationships (requiring both technical expertise and business acumen) • Identify, assess and implement new suppliers into outsourced supply chain • Work with Legal to negotiate and implement new contracts (TA’s, Supply Agreements (commercial and development) to add value to the portfolio • Forecasting and inventory management • Provide expert due diligence support for in- and out-licensing products as required • Provide specialised technical CMC input to project teams, including defining and implementing product development plan to ensure optimum target product profile is met and maximising value • Support regulatory filing’s (IND, IMPD, NDA, BLA), including preparing CMC sections as required • Support setting of CMC budgets and ensure adherence to this budget throughout the product lifecycle Requirements • experience in pharmaceutical development and manufacturing • Excellent understanding and hands –on working knowledge of cGMP, quality and regulatory requirements for clinical and commercial material • Demonstrated ability to successfully manage outsourced manufacturing and QC contractors Qualifications The position requires a degree in a relevant scientific discipline. Salary Competitive based in London http://www.newscientistjobs.com/jobs/job/senior-pharmacy-team-leader-cambridgeshire-200627779.htmMon, 02 Nov 2009 11:43:38 +0000164383We are currently looking for a Pharmacy Team Leader to join a leading contract research organisation in Cambridgeshire. To develop and lead a team of formulation scientists and technicians preparing formulations in support of pre-clinical studies. The Senior Team Leader is responsible for planning the workload and maintaining quality. Ensure that the GXP services meet current and future world-wide regulatory compliance and internationally recognised quality standards. Maintain an up to date knowledge of scientific advancements and developments relevant to Pharmacy procedures. Disseminate knowledge of new scientific advancements and developments to Pharmacy staff. Plan, organise and oversee the workload of the Pharmacy formulation areas at HRC. Liaise closely with the Pharmacy Manager ERC regarding scheduling and resource. Ensure all work generated by the team complies with regulatory requirements is of the highest quality data and all formulations are issued in a timely manner. Ensure that all requests for work are dealt with promptly and effectively to the required regulatory and scientific standards. Review and approve Pharmacy methodology ensuring it is fit for purpose and scientifically valid. Review and approve Pharmacy documentation. Prepare or amend Standard Operating Procedures. Review Protocols and ensure the requirements of Pharmacy are clear, understood and achieved, discussing any concerns with the Study Director. Ensure all errors are thoroughly investigated and reported following appropriate Company procedures. Assist in the maintenance of quality metrics and propose solutions to quality issues. Ensure that common working practices are adopted and maintained. Drive process improvements within the Department. Drive the evaluation, validation and implementation of new technologies and equipment, including IT systems. Act as a key contact for internal and external customers, ensuring customers receive prompt and appropriate responses to queries and are regularly updated where requested. Maintain agreed customer service levels. Host Sponsor tours and regulatory inspections and maintain a thorough knowledge of current departmental issues. Lead and motivate an effective team. Assist in the overall management of HRC Pharmacy including: Assisting with revenue recognition Assisting with recruitment and salary reviews Performance review Health & safety Attendance monitoring Absence management To apply for this position, candidates must be eligible to live and work in the UK Matchtech Group Plc is acting as an Employment Agency in relation to this vacancy. http://www.newscientistjobs.com/jobs/job/senior-formulation-scientist-inhalationgfm54888-kent-200627390.htmMon, 02 Nov 2009 11:03:05 +0000170104NES Scientific are recruiting for a contract Scientist based at our global pharmaceutical client within there Inhalation department. You will be supporting the development of dry powder inhaled formulations and associated manufacturing processes. The role will involve the formulation of novel candidate for further process and evaluation, physical and analytical characterisation of prepared formulations, assist in the scale up of lead formulations and support technology transfer of related drug product manufacturing. You will ideally have a first degree or equivalent in a pharmaceutical science or related subject and have proven experience in a commercial pharmaceutical laboratory, especially within the analysis of small molecules, liquids or solids formulation and manufacturing techniques. Preferably with HPLC, DPI development, particle sizing and working to GLP/GMP. if this is you apply now to Geoff Flavell-Matts at NES now. http://www.newscientistjobs.com/jobs/job/formulation-specialist-senior-scientist-gfm-54801-nottinghamshire-200627363.htmMon, 02 Nov 2009 10:38:30 +0000170096NES UK are recruiting a Formulation Specialist/Senior Scientist for our pharmaceutical client based at their modern facility in the East Midlands. the role will be for someone with extensive experience in the formulation of inhaled products to join the respiratory development team of this market leading company. The successful candidate will have a track record in the development of formulation for use in inhaled products. This experience could come from either the development of more traditional blended formulations or from the development of spray dried or other small molecule formulations. You will also have to provide innovative formulation solutions. You will have a higher qualification in science and have experience within a COMMERCIAL pharmaceutical environment. Excellent communication and team working skills are essential Please apply via email to Geoff Flavell-Matts at NES