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<p><strong>As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.</strong></p><p><strong>Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.</strong></p><h3><strong>QC Scientist I</strong></h3><p>The PDS Analytical Development &amp; GMP Scientist is a joining link between Analysts and Team Leader/Supervisor, working with clients and handling the laboratory activities.</p><h4><strong>What will you do</strong></h4><ul><li>Ensures both the execution and constant supervision of analytical laboratory activities for projects assigned in accordance with GMP requirements, supporting analysts in problems solving for analytical activities relating to API / DS and finished products (Release and Stability)</li><li>Draws up analytical specifications, study protocols and reports, analytical methods and SOPs in compliance with current regulations (current EU GMP, US GMP) and company quality standards.</li><li>Coordinates the customer's management with the aim of maintaining a high level of customer happiness and completing the required activities on schedule.</li><li>Participates in calls/meetings with customers to support the discussion on technical topics for their area of expertise.</li><li>Identifies the requirements for analytical technology transfer from customers, then ensuring the accurate and effective transfer to the laboratories</li><li>Handles laboratory investigations (Out of Specification and Deviation Reports)</li></ul><h4><strong>How will you get here</strong></h4><h5><strong>Education</strong></h5><ul><li>Degree in CTF, Chemistry, Biology or other similar fields</li><li>Diploma Chemical/Laboratory technician certificate</li></ul><h5><strong>Experience</strong></h5><ul><li>Experience in pharmaceutical industries</li><li>Multi-year experience in Quality Control</li></ul><h5><strong>Knowledge, Skills, Abilities</strong></h5><ul><li>Knowledge of the main techniques of chemical-physical and biochemical analysis and validation of analytical methods</li><li>Knowledge of GMP and national/international regulations</li><li>Good problem-solving abilities</li><li>Proficiency in Microsoft Office suite and both analytical and statistical software (Empower, MiniTab, Sample Manager)</li><li>Be prepared to work with conflicting priorities and under time constraints.</li></ul><h4><strong>Work Schedule</strong></h4><ul><li>Other</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li>Office</li></ul><p><a target="_blank" rel="noopener noreferrer" href="http://jobs.thermofisher.com"><span style="color:#263238;"><strong>Apply today! </strong></span><span style="color:#0d47a1;"><strong>http://jobs.thermofisher.com</strong></span></a></p><p>Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.</p><p>Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.</p>

QC Scientist I

<p><strong>Just – Evotec Biologics, wholly-owned by Evotec SE, is a unique platform company that integrates the design, engineering, development, and manufacture of biologics. With deep experience in the fields of protein, process and manufacturing sciences, the Just team came together to solve the scientific and technical hurdles that block access to life-changing protein therapeutics; from the design of therapeutic molecules to the design of the manufacturing plants used to produce them. Just&#39;s focus is to create access and value for a global market through scientific and technological innovation.</strong></p>
<h3><strong>SENIOR SCIENTIST</strong></h3>
<p>Aptuit, an EVOTEC Company, is a worldwide Pharmaceutical Organization, collaborating with all the major Pharma and Biotech companies in support of various drug discovery and development projects. To efficiently support current activities and needs, we are looking for a <strong>Senior Scientist</strong> to join our Analytical Sciences team in Verona. ​</p>
<h4><strong>Responsibilities:</strong></h4>
<ul>
<li><p>She/He will be expected to provide key contributions with ideas and expert advices to the various phases of drug development, from API to drug product formulation development/optimization for the analytical activities and the Physical properties characterizations.</p>
</li>
<li><p>Develop and validate analytical methods for API (mainly small molecules) and drug products characterization (Solid orals/Liquid orals and inhalation dosage forms).</p>
</li>
<li><p>Perform analytical testing according to standard operating procedures for batch release and stability studies (Assay/Imps by HPLC, Dissolutions) meeting the expected cGMP quality and agreed timelines.</p>
</li>
<li><p>Contribute to the solid-state characterization of the APIs and the physical properties of the drug products and intermediates by a varierty of techniques such as : XRPD, DSC/TGA, DVS, SSA, PSD, Optical/Electronic Microscopy, MicroRaman Spectroscopy, True/Bulk/Envelope Density, Flowability).</p>
</li>
<li><p>Exercise professional judgement to identify analytical issues and support the QA team, with key decisions, to drive the preliminary Laboratory Investigations and extended investigations related to the release and stability of the products;</p>
</li>
<li><p>Generates high quality documents including methods, operating instructions, protocols, and reports.</p>
</li>
<li><p>Give written/oral update/presentation to the customers as representative of the technical area of expertise;</p>
</li>
<li><p>Support in setting preliminary specification for development stability study during the discussion with the Clients;</p>
</li>
<li><p>Collaboration with all the personnel involved in the project activities (Clients, analytical team members, formulators, Scientific Project Leaders, Project Managers);</p>
</li>
<li><p>Report out-of-specification data (OOS) and out-of-trend data to the Manager;</p>
</li>
<li><p>Ensure the traceability of all the operations conducted according to cGMP.</p>
</li>
</ul>
<h4><strong>Qualifications:</strong></h4>
<ul>
<li><p>Degree in Chemistry, Chemistry and Pharmaceutical Technology or similar. MS and/or PhD will be considered a plus;</p>
</li>
<li><p>Good written and spoken English;</p>
</li>
<li><p>Good knowledge of Microsoft Office applications;</p>
</li>
<li><p>Good knowledge of cGMP guidelines;</p>
</li>
<li><p>At least 5 years of work experience in the analytical sector all in Pharmaceutical companies and GMP environment;</p>
</li>
<li><p>Strong background in chromatographic techniques (HPLC/UPLC/GC-MS);</p>
</li>
<li><p>Proven theoretical and practical expertise in the most traditional material science technologies such as x-rays powder diffraction, thermal analysis, spectroscopy (Raman and IR), particle size distribution determination, dynamic vapour sorption, microscopy is required.</p>
</li>
<li><p>Precise management of activities, Commitment to the assigned deadlines and ability to deliver tight deadlines;</p>
</li>
<li><p>Good knowledge of Empower 3 software;</p>
</li>
<li><p>Good interpersonal and teamwork skills, precision and flexibility;</p>
</li>
<li><p>Good knowledge of the specific guidelines and relevant regulatory EP and USP monographs;</p>
</li>
</ul>
<p>In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.</p>


Senior Scientist

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