FSP - Logistics Coordinator

<p style="text-align:left"><b>Work Schedule</b></p>Standard (Mon-Fri)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Adherence to all Good Manufacturing Practices (GMP) Safety Standards<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p><p></p><p>Shift: Full-Time; Monday – Friday; 7am-3pm EST</p><p><b>ONSITE: </b></p><p>This is a fully onsite role based at our customer’s site in <b><i>King of Prussia, PA.</i></b> We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.  </p><p>Must be legally authorized to work in the United States without sponsorship. </p><p>Must be able to pass a comprehensive background check, which includes a drug screening. </p><p>At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100&#43; countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.</p><p>Thermo Fisher&#39;s clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.</p><p>Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.</p><p><b>Key responsibilities:</b></p><p>As a Logistics Coordinator you will provide resources to execute the Sterile Operations, Sample Management and Logistics functions in Upper Merion building 29, which will have accountability for the following activities:  Routine technical operations in area of assignment under general supervision, such as logging in materials, inspection for damage and cold chain compliance, maintaining inventory records, sampling of raw materials, and updating materials in conformity to GMP standards.</p><ul><li>Supports storage of materials in appropriately identified manner in suitable environment with minimal supervision.</li><li>Maintain inventory records.</li><li>Performs packaging of materials for shipment with limited supervision.</li><li>Maintains housekeeping of the area and restocking of general supplies.</li><li>Coordinates transfer of excipients, components, and samples to support clinical and pre-clinical manufacture and component processing orders under guidance.</li><li>Manage inventories and schedule routine activities appropriately with oversight.</li><li>Assist in the preparation of metrics and key KPIs for the area.</li><li>will participate in department consumables storage and stocking programs.</li><li>may be asked to support administrative tasks such as procedure revision support, template revision support, records filing, records archiving, and other tasks as needed.</li><li>All job functions will be performed according to procedure and in accordance with cGMPs, Standard Operating Procedures, and Client safety codes and regulations.</li><li>Escalates potential risks to the business for consideration by management.</li><li>Assist and contribute to GMP and safety self-inspection activities.</li><li>Supports the reporting and maintaining of area metrics as appropriate.</li><li>Zero instances of data falsification or data integrity issues by PPD staff.</li><li>has basic computer skills including Word, Outlook, and ability to navigate simple website interfaces.</li><li>Must be a committed team player prepared to work in and embrace a team-based culture.</li><li>Support the upgrades/transition of the Inventory Management System used by the Sterile Operations team to support business processes/activities (e.g. COMET to SAP, etc).</li></ul><p><b>Education and Experience: </b></p><ul><li>High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification</li><li>Technical positions may require a certificate</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 0-2 years).</li><li><i>In some cases an equivalency, consisting of a combination of appropriate education, trainingand/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</i></li></ul><p><b>Knowledge, Skills and Abilities: </b></p><ul><li>Applies basic knowledge and supports continuous improvement activities utilizing available tools where applicable that support continued adherence with industry regulations, Global Quality Policies (GQP 3201A (Document Management and Control) and GQP 3201B (Data Management and Control)) and supporting business procedures.</li><li>Proactively communicates the status of assigned compliance systems support and problem resolution to appropriate contacts and escalates issues when needed to supervision.</li><li>Applies metric generation and reporting support for Sterile Ops led processes as directed.</li><li>Works collaboratively and embraces Client’s Code of Conduct to effectively implement solutions. Develops and maintains productive relationships in the workplace and leverages internal networks for support.</li><li>Supports the identification and implementation of strategies to improve the qualities and efficiencies of Sterile Ops processes, systems and results. Develops and maintains understanding of current technologies and professional concepts.</li><li>Assists with scheduling and planning work to meet priorities set by the Client. Follows daily and weekly priorities to meet timelines and recommends procedures and policies to supervision.</li></ul><p><b>Working Environment: </b></p><p>Below is listed the working environment/requirements for this role:</p><p>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</p><p>Able to work upright and stationary and/or standing for typical working hours.</p><p>Able to lift and move objects up to 25 pounds</p><p>Able to work in non-traditional work environments.</p><p>Able to use and learn standard office equipment and technology with</p><p>proficiency.</p><p>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</p><p>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</p><p><b>Benefits</b></p><p>We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!</p><p></p><p></p><p></p><p></p><p></p>