Experienced Analyst/Technician for QC Chemistry

<p>Are you an experienced analyst and eager to join a fast-growing pharmaceutical company? Now you have a unique opportunity as we are looking for an analyst with flair for Chemistry who <span>shares our passion, drive, and energy – what we call <b>Genki</b> – </span>to join QC Chemistry.</p><p></p><p><b>About the QC Chemistry department</b></p><p><span>The QC Chemistry department currently consists of &gt;35 dedicated employees (analysts, scientists, student helpers, and a leadership team). The department</span> consists of 3 teams and supports the global release of commercial Drug substance and Drug Product (DS/DP) and raw material for our clients with various <span>purity/impurity/pharmacopeia</span> chemistry methods (e.g. CE-SDS, ICE, SDS-page, HPLC/UPLC, Appearance, pH, Osmolality, SoloVPE/UV) as well as the support to the Drug Substance manufacturing by ensuring TOC changeover and cleaning validation testing, gas (CO2, O2 and N2) and water testing. Method transfers and method validation and qualification are becoming a key deliverable for the department with the many new clients due to the site expansion of DS manufacturing together with establishment of a Fill &amp; Finish facility for drug product (DP).</p><p></p><p>The width of methods from simple to complex, the amount of new client methods transferred, new instruments, continuing testing of current legacy products, stability testing, client audits and authority inspection ensure that the department is in constant change where improvements are prioritized and welcomed. <span>And not least we perform qualification of controls and reference standards, handle deviations, CAPAs, invalid assays, OOS and Change Controls and much more. All this is part of our daily activities in respect of getting the commercial products out to the patients.</span></p><p></p><p><b><span>About the Position</span></b></p><p><span>As an analyst in QC Chemistry, your expertise will be vital in our team performing testing of raw materials and release tests for Drug Substance, Drug Product, and stability samples in an GMP environment. Your role will not only involve analyzing samples to guarantee the highest quality standards in medicine but also expand to taking part in the transfer of new methods in collaboration with Analytical Development, continuously improving our processes and analyses, challenging the status quo contributing to a safe and healthy work environment focused on excellent teamwork and fostering the OneQC spirit</span></p><p></p><p><span>The department and our organization will continue to expand and adapting due to the site expansion where we the next 2 years expect a 2 x DS manufacturing and one new DP manufacturing facility on site Hillerød. </span></p><p></p><p><b>About FUJIFILM Life Science Biotechnologies and our Quality Control Department</b></p><p>FUJIFILM Life Science Biotechnologies (FLBD) is a world leading Contract Development Manufacturing Organization (CDMO) serving clients in the pharmaceutical industry – from pre-clinical investigations to commercial GMP production. Our overall mission is to “Advancing Tomorrow’s Medicines” and we like to invite you to be part of that journey.</p><p></p><p>Our Quality Control (QC) department at site Hillerød consists of approximately 260 employees divided into different support teams and three testing teams. In QC we strive towards a OneQC team spirit where we help and support each other across teams not only to reach our goals but also to support a high level of collaboration and possibilities for personal development. The pillar in our QC department is our employees – our success is only possible due to competent and dedicated colleagues, who wants to make a difference for QC, our site, our clients, and patients all over the globe. As a leading CDMO company we, in QC, are obligated to continuously improve our way of working creating a dynamic and inspiring environment with huge individual co-decision making due to our flat organizational structure.</p><p></p><p>The culture at FLBD is key if you ask our employees and besides a competitive salary and bonus package, we offer health insurance, massage and physiotherapy, health check, fitness center, possibility to work from home etc. FLBD also has a canteen arrangement incl. Friday brunch and monthly afternoon cake, just as we have a “bell ringing” tradition when reaching important milestones.</p><p></p><p><b><span>Qualifications Required:</span></b></p><ul><li><span>An education as laboratory technician or medical laboratory technician</span></li><li><span>A proven track record with extensive experience in a GMP setting and proficiency in a range of analytical techniques</span></li><li><span>Professional proficiency in English, both written and spoken</span></li></ul><p></p><p><span>At FLBD we put people first and we always look for candidates with the right combination of personality and skills. FLBD will, as any other modern companies, ask our employees for