improvement - Identification and evaluation of business driven variations to service delivery – local approval and escalation REQUIREMENTS - BSC - 5 years’ experience of Higher level technical qualifications in engineering - Knowledge of the R&D process and requirements
technical support service to all European customers, visit them and carry out pilot and industrial trials at their sites as required. What is more, for about 50% of the time you will work at a laboratory to provide a timely and accurate response to all technical enquiries from customers and distributors.To
orientation and with big picture view on inside processes and market reality. You should easily understand technical issues. Strong motivation to sell, market understanding and previous experience in building sales teams is required. What can you gain?Very interesting role with ambitious aims, nice work
To maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; benchmarking state-of-the-art practices; participating in professional societies; ProfileGood standard of general education; Proactive manager capable of
including submissions and registrations of new products, Documentations, Technical Files, being in contact with (local) authorities and audits. • Experience of submissions and registrations in Asia and America is a big plus • Understanding of ISO 13485 and/or FDA 21 CFR part 820 is a big plus
of subordinate areas (technical services and vehicle operations, insurance and claim, purchase and pricing, re-marketing) Management and monitoring of plans for subordinate areas. Coordination of the activity of subordinate organisational units of the operational department. Evaluating new market
alignment of future capabilities with strategic business plans. Champion the process of design, development, implementation and qualification for R&D driven and R&D supported CAPEX and Innovation projects in a complex technical environment. Build and lead the R&D Engineering organization at the Nijmegen
experience with Regulatory Affairs for Medical Devices • Evidence of experience in a senior management role • Excellent knowledge of ISO 13485 and 9001 • Experience as lead in audits • Extensive knowledge of FDA 510 K, Risk management ISO 14971, CAPA Management, Lean Six Sigma, 21 CFR Part 11, Technical
regulatory variations: - Writing IMPDs as far as CMC is required - Registration of files and variations for EU - Writing Module 2 of regulatory files that can are to be submitted through eCTD Modules Report to RA Director REQUIREMENTS MSc. in life science with relevant
be a medical contact person for medical community in the area of Oncology/ IBD throughout Poland. In all above you will report to the Medical Director. Accountabilities include: Medical/Scientific Affairs Use specific disease and product knowledge to develop Takeda in a given therapy area; i.e. answer medical/technical unsolicited enquiries from HCPs, provide accurate and non-promotional scientific ...
sciences; has 4-7 years’ experience in developing consumer (health) care products in a small/medium-sized company; knows how to manage projects and set up analytical methods; is able to write scientific parts of product technical files for registration of new products; has basic knowledge of
possibilities. They can teach you the technical ins and outs of the product. This allows you to build the client base in the way you see fit, within an organisation which stimulates personal responsibility, and of course also reap the financial benefits that follow ...
as assigned by Medical Director Seek legal support as need and ensure that all activities with third parties are subject to contractual agreement Key responsibilities and accountabilities Acting in a capacity on behalf of Norgine BV:. Medical Knowledge Center Radiopharmaceuticals - Norgine BeLux
forms. Monitoring of the quality of our products to ensure that the entire range meets quality norms that are in line with Smit & zoon’s sustainability ambition as well as being in full compliance with international regulations; You will report directly to the R&D director. Your team consists of 6
Talent philosophy • Facilitate internal resources and outside vendors in developing technical solutions for automated equipment. Interface with equipment vendors to ensure successful machine delivery, integration and manufacturing validation • Support product, platform and cost improvement programs
reducing business situations to clear and focused action plans. • Is energetic and decisive in driving ideas and activities forward Other Skills and Abilities: • This person must be ambitious, energetic, diligent, tenacious, and self-motivated. • Possess a strong technical aptitude. • Must have strong