When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. The Clinical Diagnostics Division (CDD) is a division made up of business units which develop, manufacture and market instruments and consumables that serve a broad, diverse mix of diagnostic segments. The business units include Niche Diagnostics, Biomarkers, Clinical Diagnostic Systems (includes clinical mass spectrometry), and Clinical Diagnostic Reagents. The division manages a diverse portfolio of products servicing multiple end markets. CDD maintains recognized technology and manufacturing leadership in the markets in which it serves. CDD has approximately 2,000 employees across the Americas, EMEA and APAC. Primary global business locations are in California and Virginia for the United States; primary global business unit locations also include Germany and Finland. APAC markets focus particularly in the China marketplace. The Clinical Diagnostics Division is part of the Specialty Diagnostics Group within Thermo Fisher Scientific. Position Summary: Primary responsibility will be to provide support as an Executive Assistant, you'll be at the center of fast-paced growth, using office and project management skills to support the President, Vice President, Human Resources and Vice President, Finance of the Clinical Diagnostics Division. In this role one will require discretion and diplomacy while working with stakeholders across the company, a mastery of time management, logistics planning, organization, and attention to detail will ensure flawless execution of multiple priorities. * Ensure that the respective executives get where they need to be on time through meeting scheduling and arrangement of complex global, multi-city travel. * Develop understanding of the business priorities and goals for the function; use knowledge and understanding in prioritizing meeting requests. * Schedule and coordinate complex executive meetings, bringing together geographically dispersed teams, managing logistics, and documenting follow up activities. * Collaborate and build relationships to drive results in a global-matrixed organization experiencing change and transformation. * Complete projects and special assignments by establishing objectives, determining priorities, managing time, gaining cooperation of others, monitoring progress and problem-solving. * Research, compile, summarize, and analyze information to make decisions, find answers, and respond to various inquiries from internal and external customers. * Utilize the full suite of Microsoft office products to prepare high quality correspondence, reports, and presentations. * Manage expense reporting, process vendor invoices, and support annual budget process. * Personally takes care of many matters and questions, including answering substantive questions requiring technical knowledge, but can often require research and follow up * Proactively manages projects/deliverables/due dates - following up with project owners, key stakeholders, and employees as needed to meet assigned due dates successfully. * Attends meetings and prepares minutes. * Demonstrates both the flexibility and adaptability required to meet the dynamic nature of the business * Maintains confidential files and records. * Coordinate with other Executive Assistants and Administrative Staff to cover the area that is unavailable due to illness, vacation or other special circumstances. * Occasional travel coordination support after hours and on weekends. Minimum Qualifications: * Associates Degree or combination of education and experience (5 or more years), Bachelor's degree preferred * 8+ years of executive assistant experience in a professional office environment, large organization preferred * Demonstrated experience in working independently to identify, analyze, and solve problems with creative solutions. * Skilled and experienced in the art of organization and time management to juggle multiple priorities with competing deadlines. * Excellent written and verbal communication skills. Exceptional proof reading and spelling. * Solid judgment, tact, and diplomacy skills in dealing with internal and external customers as well the ability to handle highly confidential and proprietary information. * Flexible and adaptable, with the ability to respond to last-minute changes while maintaining poise and a positive 'can do' attitude * Extensive international travel management with VISA administration experience. * Expert level skills in all Microsoft office suite products, including Power Point, Excel, Outlook, Visio * Experience with Workday preferred * Experience with Concur At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer. []When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Position Summary: The Clinical Supply Chain Manager Senior (Sr. CSCM) is responsible for planning and managing designated clinical supply chain Management team activities for the Fisher Clinical Services (FCS) Clinical Supply Optimization Services (CSOS) unit. This position will work with FCS clients, packaging sites, depots, Clinical Supply Chain Managers and Drug Supply Coordinators to understand the supply chain requirements, define the supply strategy and manage clinical trial materials on the study or program level. The Sr. CSCM will provide mentorship to other members of the CSOS unit and participate in business development activities. This is a remote position that can be located anywhere within the U.S. ​ Responsibilities: Project Management: * Serves as the global project lead on assigned projects, ensuring internal project resources are focused on delivery and client satisfaction, leading by example and negotiating across geographic and functional lines * Works with both internal and client Project teams to ensure consistent communication of clinical trial material supply status. Identifies potential risks, defines and executes risk mitigation plans. * Ensures temperature excursion process is executed as required * Performs study close out activities including returned good reconciliation, inventory destruction processing, and file archiving * Develops and provides client(s) with reports on actual project spend versus budget * Negotiates effectively with clients regarding study plan without damaging relationships Clinical Supply Experience: * Provides recommendations on packaging design, distribution and blinding strategy * Plans and manages execution of initial supplies and resupplies for assigned studies * Designs and implements strategic plans to supply study drug to complex global clinical trials using sound supply chain techniques IRT Knowledge: * Provides input into user requirement specifications of Interactive Response Technology (IRT) medication management module(s) as needed. * Reviews IRT strategy to ensure it supports the strategic supply plans and ensures that IRT settings are adjusted to optimize the supply chain * Executes IRT User Acceptance Testing, if required * Leverages the inventory management capabilities of the IRT to appropriately manage studies Supply Chain Management: * Devises and implements inventory management plans that have complex supply chains * Reviews, interprets and implements supply forecast plans from internal or external source documents and tools * Executes supply chain inventory management processes in partnership with internal Clinical Supply Optimization Services team members and packaging partners. * Proactively identifies potential supply chain issues, provides analysis and recommends solutions Required Qualifications: * Bachelor's degree or higher in operations management or science-related field (equivalent work experience may be considered) * Minimum of five (5) years clinical supply chain management experience * Minimum of 5 years clinical supply chain management experience * Experience IRT/IXRS/IWVR required. * Experienced in building and managing forecasts for clinical supply chains * Knowledge of relevant cGMPs, GCPs, and other regulatory requirements * Excellent computer skills, including high proficiency with Microsoft Suite including Excel, Word and MS Project as well as the Office 365 environment. Additional Qualifications: * Significant travel (up to 25%) may be required, including international travel * Ability to independently manage priorities and workday in a remote setting * Excellent oral and written communication skills * Excellent teamwork and interpersonal skills At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer. []DUTIES: Lead CDx projects designed to expand claims of the ODxT. Test Lead a small team of scientists with minimal supervision. Manage R&D timelines and deliverables. Identify technical risks and work closely with other functional groups to identify mitigation strategies to keep project deliverables on schedule. Analyze data and present to upper management. Represent R&D at internal and customer facing meetings. Ensure design control and quality system processes are followed and deviations are properly documented. Work with Clinical Affairs to support Clinical Validation activities. Work with regulatory team to prepare pre-submission documents and sPMA submissions. REQUIREMENTS: PhD degree in Genetics, Molecular Biology, or related field of study plus 3 years of molecular biology, genetics, biochemistry, industrial laboratory, IVD product development or related experience. Employer also accepts a Master's degree plus 6 years of experience as an equivalent alternative. Must have experience or knowledge of: NGS assay development and in vitro diagnostics product development; (3 years) Experience working with pharmaceutical partners to develop companion diagnostic assays; (3 years) Development of companion diagnostic assays; (3 years) Illumina and Ion Torrent sequencing technologies; (3 years) Planning and managing execution of verification and validation studies for FDA submissions; (3 years) Writing and reviewing technical reports; (3 years) Molecular biology; (3 years) Next Generation Sequencing; (3 years) IVD product development; (3 years) Data analysis; (3 years) GMP/GLP; (3 years) and Drafting pre-submission documents and presenting data and information to the FDA. (2 years). []Position Description/Summary Responsible for cGMP manufacturing operations at the Thermo Fisher Scientific Lexington site Drug Product (DP) Fill/Finish operations. Responsibilities include: * Performing basic to complex activities on the fill finish line for production of Drug Product. * Performing critical downstream activities in preparation for fill finish of Drug Product. * Documentation of all activities in Batch Records, Logbooks, Forms, Etc. * Follows verbal and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation. * Identifies, escalates and documents events and subtle variances that deviate from normal operation; participate as needed in investigations. * Monitor processes using automated production systems and controls with limited supervision. * Equipment preparation activities including, parts cleaning, autoclaving, and room clearance. * Demonstrates ability to troubleshoot basic mechanical operations. * Post-Fill tasks will include visual inspection, secondary packaging, and environmental monitoring. * Daily Aseptic processing within a controlled isolator environment and within a BSC. * Conducts training for less experienced personnel Expectations: * Must be able to work in a fast-paced environment. * A strong attention to detail through a 12-hour shift. * Work towards solutions to given problems and operate under cGMP requirements. * Work cross-functionally with support groups such as Facilities, Engineering, Contamination Control, Quality Control and Quality Assurance. * Qualify to work in aseptic environments to complete required production activities. * Maintain facility and room inspection readiness. * Ability to lift at least 50lbs. * Ability to aseptically gown and/or sterile gown as needed. Work Hours: 8 hour Monday - Friday shift. May require overtime, evenings, weekends or holidays, as required to meet project and Manufacturing timelines. Additional Responsibilities: * Work in accordance with site and company EHS programs. * Work in accordance with regulations, detailed protocols, Batch Record's, SOP's and Work Instructions. * Prepare and process components, materials and equipment for aseptic fill finish activities, operate filling equipment and perform aseptic manipulations, able to inspect finished vials and perform labeling activities to support shipment. Knowledge, Skill and Requirements Qualifications: -Bachelor's Degree with 1-3 years of industry related experience in cGMP manufacturing. -High School diploma with 3-5 years of industry related experience in cGMP manufacturing. []Job Title: Market Development Specialist III Requisition ID: 111335BR Location: Carlsbad, CA OR Eugene, OR When you join us at Thermo Fisher Scientific, you'll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world. What will you do? The Associate Global Market Development Manager / Marketing Specialist III (assocGMD) will develop and execute marketing programs for the microplate detection platforms using a multi-channel go-to-market strategy focus. This scientific, dynamic manager will be a key member of the Protein and Cell Analysis Global Market Development team. This role is responsible for working with a broad team, including regional and business counterparts, to develop global go-to-market strategies and integrated multi-channel marketing plans to then execute on tactical projects to achieve KPI and revenue targets and other annual operating plan objectives. This position can be based out of either of our Carlsbad, CA, or Eugene, OR, campuses. RESPONSIBILITIES: * Develop strategic marketing plans for microplate washers and microplate detection instruments portfolios, including analysis of customer segments, competitor analysis, business trends, and market opportunities. * Develop and execute engaging, bold tactical marketing plans for new and/or existing portfolio products including those for microplate washers and detection instruments and associated software.. * Drive demand generation for this portfolios delivering and evaluating the quality of marketing qualified leads to the technical sales specialist team * Develop customer personas for each portfolio segment and implement a customer segmentation program to build global audiences. * Create and implement appropriate technical marketing content across digital channels, including web, video, social media, paid search and display advertising. * Develop sales force selling tools, technical training and customer facing materials in collaboration with product management, R&D, and commercial teams. * Act as a brand ambassador, understanding, upholding, and communicating our multi-brand strategy in all aspects of our marketing programs. * Coordinate with global functions to ensure consistency with brand profiles and company standards. * Interact with varying levels of internal and external personnel including direct customer communication, public presentation, and a team-focused approach. * Interact and support internal technical selling teams, with enablement in tools and training. * Work closely with regional marketing development managers to build and execute marketing programs within their regions. * May perform other related duties as required and/or assigned. How will you get there? Education: * Bachelor's degree in Biology, Biochemistry or related discipline. Experience: * 2+ years of experience developing a marketing strategy and successfully implementing marketing plans for highly technical reagent platforms requiring a complex selling approach * Knowledge of the following key competencies: 4Ps and marketing mix, marketing communication, communication channels, channels-to-market, segmentation, value proposition and marketing program development and execution. * Technical knowledge in the flow cytometry platform markets * Experience with product area marketing plans, general knowledge of operating plans or industry practices for promoting and selling similar products. * Experience writing technical scientific content with ability to develop messaging for sales and customer facing materials. * Exceptional communication skills as well as analytical, project management and planning skills necessary. * Ability to manage complexity of multiple product lines with distinct go to market strategies. * Strong business acumen and customer focus are essential. * Experience with marketing and voice of customer VOC. * A strong record building alignment in cross-functional teams and navigating within a matrix organization to achieve goals. * Travel is required. (25%) Preferred Qualifications: Masters of Science and/or PhD in life sciences discipline At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer. []When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. What will you do? A manufacturing laboratory position in an ISO certified environment supporting Thermo Fisher Scientific Immunoassay Systems product line. The associate should have exposure and understanding through either reading or preferably hands on experience in such biochemical lab techniques as listed below: Key Responsibilities: * Understand and follow:* Safe lab practices * Good documentation practices. The associate is expected to maintain detailed documentation and implement updates in support of ISO requirements * Commit to producing and maintaining the highest standard of quality in antibody production * Ensure on-time delivery of production work and projects * Perform with assistance of batch records, standard work instructions, operating procedures or shadowing with a trained associate: * Protein isolation and purification * Chromatography (affinity, ion exchange, size exclusion). FPLC experience helpful * Protein modification (cross linking, fluorescent, protein and small molecule conjugations) * Protein lyophilization * Carrier protein conjugations with peptides or fusion proteins * Antibody purification / modification experience * Antibody validation via various functional tests, i.e. WB / ELISA / IHC / IP / IF / FACS * SDS-PAGE * Small and large scale buffer preparations * Protein/enzyme assays * UV / VIS Spectrophotometry measurements * Set up and take down of labware * Maintain accurate inventory * Assist the manufacturing support associate and/or material handling in cycle counting or physical inventory as required How will you get here? Education * Minimum of a Bachelors of Science degree in a Biochemical / Biological sciences, Chemistry, or Life science emphasis; Masters degree, preferred Knowledge, Skills, Abilities* Demonstrate 0 to 2 years experience. It is desired that the associate have prior experience in a manufacturing role with a solid understanding relevant to corporate goals, objectives and strategies * Demonstrate general hands on lab skills as would be acquired in a 4 year Bachelors level science degree. Experience in organic chemistry is helpful * Able to demonstrate analytical thought process and understand experimental design when explained * Experience with aseptic handling technique. Autoclave experience is helpful. * Ability to lift 50 pounds * Understanding of molar theory * Exposure to working with animal and human blood, cells, sera and tissues * Hazardous Waste Generation/Management: Associates in this position may as part of their job activities generate or manage hazardous waste as defined by the Illinois Environmental Protection Agency. Individuals in this position are required to receive initial hazardous waste training within the first 30 working days of assignment. The initial waste training shall include but not be limited to the following general categories: Identifying hazardous and solid waste, hazardous waste management, recycling, treatment and disposal, emergency preparedness, record keeping, pollution prevention and waste reduction. Following initial training the Associate in this position will receive annual refresher training in the same topic field as listed above. Associate should be comfortable working frequently with organics, including flammable solvents, strong acids / bases, potential biohazards (including raw animal serums), large scale bacterial cultures, and hazardous chemicals This position has not been approved for Relocation Assistance. At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission-enabling our customers to make the world healthier, cleaner and safer. []When you're part of the team at Thermo Fisher Scientific, you'll do important work. You'll have the opportunity to grow and learn in a culture that empowers your development. We have created an inclusive, global environment that values the power of diverse talent, backgrounds, and experiences to drive speed, productivity, innovation, and growth.Our internship program will give you a chance to get real world business experience and build your network before graduation. We are seeking an energetic, responsible intern to join our growing organization. In this position, you will be expected to learn the ins-and-outs of our daily routines and procedures. You will focus on learning how our organization runs, and can be expected to gain valuable insight that can further your interest in your chosen career field. Summary:The selected Intern will work with the PMO and Commercial Applications Leadership teams on initiatives related to the RPA (process automation) and ERP readiness projects. The Intern will be responsible for coordinating/facilitating the tasks within these projects in addition to being accountable for completing a couple of them by gathering information and working closely with the PMO team. The position starts in May or June, paid working 40 hours per week through August. Essential Functions* Responsible for charting out plans to accomplish the assigned tasks * Responsible for reporting out on assigned tasks as needed * Support GPO's (global process owners) in requirements workshops for ERP readiness. * Complete needed process documentation output for as is and proposed future state. * Drive process analysis utilizing Celonis to support current state diagnostic and identify improvements leading the future state. Qualifications:* Excellent organizational and communication skills * Self-motivated, team player and ability to work in a fast-paced environment * Excellent working knowledge of common IT applications/systems. * Attention to detail and a passion for driving execution at a detailed level * Prior experience with process automation and enterprise resource planning systems a plus. Education Level:* Pursing a Bachelor's Degree in Data Science, Supply Chain or Management Information Systems []

As the world’s leader in serving science, Thermo Fisher Scientific's professionals develop critical solutions—and build rewarding careers. They help customers in finding cures for cancer, protecting the environment, making sure food is safe, and so much more. When you #StartYourStory with Thermo Fisher, you are guaranteed meaningful work - both personally and professionally.