Manager Bioanalytics Jobs Vacancy in Philip Morris International
Philip Morris International urgently required following position for Manager Bioanalytics. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.
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Manager Bioanalytics Jobs Vacancy in Philip Morris International Jobs Details:
Are you inquisitive and self-driven? Will you make a difference to our company and your colleagues around you? If the answer is yes, ja, oui or igen, then we’d like to hear from you. We are looking to recruit an action-oriented problem solver with a PhD in Chemistry, Life Science or related technical / scientific discipline, with at least 5 years of relevant professional experience with a Contract Research Organization (CRO), Research & Development unit within the pharmaceutical / healthcare industries, or translational academic research organizations. You should possess technical and scientific knowledge focused on analytical and bioanalytical method development, validation and laboratory operations. You should possess in-depth knowledge preferably with hands-on experience on a broad range of analytical and bioanalytical platforms and work flows in toxicology studies and life science research, i.e. LC/GC, LC-MS/MS, FACS, IHC, clinical chemistry, hematology, molecular biology and other characterization tools for chemical and biological entities and systems. Good understanding of regulatory guidelines such as FDA, ICH, OECD GLP and TGs related to in vivo toxicology study and method validation is preferred. You should also have experience in managing R&D teams and projects, as well as possess excellent communication and influencing skills. RISE TO THE CHALLENGE Philip Morris International Research Laboratories Pte Ltd is seeking a talented individual to join our team. You will be responsible for leading, motivating and developing the bioanalytics team in order to deliver functional execution of in vivo studies on time and within budget whilst ensuring compliance with pertinent guidelines and scientific standards. The bioanalytics team handles a broad technical portfolio of clinical chemistry, hematology, cell / molecular biology assays, biomarker quantitation, chromatography, and mass spectrometry, and you are responsible for building functional capability and capacity for efficient execution of in vivo toxicology and studies at the center, and to ensure scientific and technical rigor in the responsible areas to support the company's science and innovation pipelines. You will also plan, direct and manage the operations for the bioanalytics laboratories in areas of resource, budget, timelines & risks; update & maintenance of equipment, workflows & laboratory information systems; and development & implementation of new assays, test methods, equipment, workflows, & systems. Responsibilities: • Lead, develop and motivate the bioanalytics group, which includes objective setting and performance evaluation, providing technical and people leadership, developing learning & training plan to facilitate individual's development, providing regular feedback. • Oversee the overall activities in the bioanalytics laboratories to ensure SOP / technical guides and training are available and adequate for the technician to perform their day to day tasks, and the test results are turned around within the time in agreement with the study requirements and/or stakeholders. Ensure that the methods, equipment, systems, and workflows are fit for purpose, up to date and efficient. • Keep track of the latest technological advancement in the field, then assess, adopt and provide expertise for developing and implementing new / innovative techniques, assays, methods, capabilities that will enable / accelerate company's scientific project portfolio execution in particular for scientific substantiation of Reduced Risk Products (RRP) and exploration of adjacent therapeutic areas. • Represent the functions to coordinate and liaise with cross-functional units and stakeholders on the planning, resourcing, execution, data analysis and reporting of in vivo (and ex vivo, in vitro) pre-clinical studies within R&D. Foster a culture of collaboration and enable frequent technical exchange across the network. • Ensure the day to day laboratory operation is smooth and efficient, devise and implement continuous improvement projects to ensure the laboratory operation and systems keeps up to best practices. • Participate in establishing and maintaining an adequate, current and effective Quality Management System and assume ownership roles for the business area, systems, equipment and SOPs when applicable. Support quality / compliance inspections and audits conducted by both internal and external parties. FIND A NEW PATH Our company offers you a fresh perspective. Here, you will never stop exploring and discovering. We take on-the-job learning to another level, giving you every opportunity to develop your career and reach your full potential. With innovative technologies, services, and processes, backed by a competitive salary and compensation package, you will work in a professional setting with clients and team members from all over the world. GOT SOMEONE IN MIND? If you believe you would be a good fit to the requirements of the role, please submit your application online by 31 January 2018. Only candidates who fit the hiring requirements will be contacted. The successful candidate will be hired on the local employment terms and conditions in Singapore.