Work Schedule First Shift (Days) Environmental Conditions Office Job Description 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+ 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their dedication to accuracy and quality to deliver groundbreaking innovations. <ul><li>Department: Mass Spectrometry, GMP labs</li><li>Location: Middleton, WI - Lab Based</li><li>Notes: Full-time, Benefits, Annual Bonus, 401k Match, PTO, Relocation Assistance Available</li></ul> Discover Impactful Work: Conducts and provides technical mentorship on scientific method development and validation projects and/or other specialty technologies studies OR performs troubleshooting for own and others instruments, methods, procedures, and in writing protocols and reports. Designs and implements method development/validation and/or extractable/leachable studies independently and interprets and reviews analytical data for self and others OR designs and performs multiple stability and inhalation procedures as well as assists others in performing routine maintenance and troubleshooting on multiple instruments (GC, ICP-MS, LC/MS, GC/MS etc.) and multiple detection techniques (UV, FL, CAD, ELSD, IC etc.), methods and procedures. Routinely acts as the technical project leader for multiple projects, provide updates, reviews and evaluates data, writes reports and protocols. A day in the Life: <ul><li>Independently performs analytical method development/optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds or equivalent levels of expertise and experience in mass spectrometry or other related areas such as structural elucidation or extractable leachable testing in a variety of formulations and/or delivery systems. Designs and executes experiments independently for self and others.</li><li>Writes, reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.</li><li>Leads analytical (procedural and instrumental) troubleshooting sessions.</li><li>Assists business development group in technical sales and marketing, and presents posters at technical conferences.</li><li>Leads in preparation and implementation of SOPs and quality systems, as well as developing innovative technology and in evaluating and implementing new capabilities.</li><li>Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.</li></ul> Keys to Success: Education and Experience: <ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to BS degree plus 8+ years' of experience or MS plus 7+ years' of experience, or PhD plus 4+ years' of experience).</li></ul> In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: <ul><li>Intermediate knowledge of general chemistry and separation science</li><li>Intermediate knowledge of liquid chromatography mass spectrometry (LC-MS) and its application in large molecule analysis</li><li>Full understanding of laboratory requirements, SOPs, ICH guidelines, USP requirements and FDA guidance</li><li>Full knowledge of technical operating systems</li><li>Ability to independently optimize analytical methods</li><li>Ability to independently perform root cause analysis for method investigations</li><li>Proven technical writing skills</li><li>Proven problem solving and troubleshooting abilities</li><li>Effective written and oral communication skills as well as presentation skills</li><li>Time management and project management skills</li><li>Ability to mentor others on technical operating systems</li><li>Ability to independently review and understand project proposals/plans</li><li>Ability to work in a collaborative work environment with a team</li></ul> Physical Requirements / Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: <ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds.</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul> 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 with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process. <ul><li>This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.</li></ul>

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description 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+ 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence. Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. Performs self-review for own data prior to QC submission. A day in the Life: <ul><li>Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and /or biological matrices for stability and analytical testing.</li><li>Works with multiple functional groups to meet business needs.</li><li>Plans and organizes work with periodic supervision.</li><li>Sets up and maintains analytical instrumentation.</li><li>Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.</li><li>Ensures QA findings are addressed appropriately.</li><li>Aids and training to other team members.</li><li>Problem solving, either independently or with assistance pertaining to extraction and/or instrumentation problems.</li><li>Communicates project status to project leader.</li><li>Performs work assignments accurately, and in a timely and safe manner.</li><li>Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).</li><li>Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.</li></ul> Qualifications - External Keys to Success: Education <ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 6+ years).</li><li>In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</li></ul> Knowledge, Skills, Abilities <ul><li>Demonstrated knowledge of multiple applicable techniques such as: HPLC, GC, MS, Dissolution Testing, Inhalation Testing, Biopharmaceutical Testing, Karl Fischer, UV-Vis, FT-IR, TOC</li><li>Proficient in Microsoft Excel and Word</li><li>Proven ability to interpret data by performing trend analysis</li><li>Proven ability in technical writing skills</li><li>Ability to independently optimize analytical methods</li><li>Proven problem solving and troubleshooting abilities</li><li>Good written and oral communication skills</li><li>Time management and project management skills</li><li>Ability to work in a collaborative work environment with a team</li></ul> Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: <ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds.</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul>

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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+ 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their dedication to accuracy and quality to deliver groundbreaking innovations. <ul><li>Department: Cell Lab, GMP labs</li><li>Location: Middleton, WI</li><li>Notes: Full-time, Benefits, Annual Bonus, 401k Match, PTO, Relocation Assistance Available</li></ul> Discover Impactful Work: Conducts and provides technical mentorship on scientific method development and validation projects and/or other specialty technologies studies OR performs troubleshooting for own and others instruments, methods, procedures, and in writing protocols and reports. Designs and implements method development/validation and/or extractable/leachable studies independently and interprets and reviews analytical data for self and others OR designs and performs multiple stability and inhalation procedures as well as assists others in performing routine maintenance and troubleshooting on multiple instruments (GC, ICP-MS, LC/MS, GC/MS etc.) and multiple detection techniques (UV, FL, CAD, ELSD, IC etc.), methods and procedures. Routinely acts as the technical project leader for multiple projects, provide updates, reviews and evaluates data, writes reports and protocols. A day in the Life: <ul><li>Independently performs analytical method development/optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds or equivalent levels of expertise and experience in mass spectrometry or other related areas such as structural elucidation or extractable leachable testing in a variety of formulations and/or delivery systems. Designs and executes experiments independently for self and others.</li><li>Writes, reviews and critiques study protocols, project status reports, final study reports and other project-related technical documents.</li><li>Leads analytical (procedural and instrumental) troubleshooting sessions.</li><li>Assists business development group in technical sales and marketing, and presents posters at technical conferences.</li><li>Leads in preparation and implementation of SOPs and quality systems, as well as developing innovative technology and in evaluating and implementing new capabilities.</li><li>Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.</li></ul> Keys to Success: Education and Experience: <ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to BS degree plus 8+ years' of experience or MS plus 7+ years' of experience, or PhD plus 4+ years' of experience).</li></ul> In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: <ul><li>Cell Bioassay experience</li><li>GMP experience</li><li>Full understanding of laboratory requirements, SOPs, ICH guidelines, USP requirements and FDA guidance</li><li>Full knowledge of technical operating systems</li><li>Ability to independently optimize analytical methods</li><li>Ability to independently perform root cause analysis for method investigations</li><li>Proven technical writing skills</li><li>Proven problem solving and troubleshooting abilities</li><li>Effective written and oral communication skills as well as presentation skills</li><li>Time management and project management skills</li><li>Ability to mentor others on technical operating systems</li><li>Ability to independently review and understand project proposals/plans</li><li>Ability to work in a collaborative work environment with a team</li></ul> Physical Requirements / Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: <ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds.</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul> 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 with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process. <ul><li>This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.</li></ul>

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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+ 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: Performs complex laboratory analysis of pharmaceutical products and proficiently uses analytical instrumentation, calculates and analyzes data and records data in adherence with PPD SOP's and the industry. Routinely acts as the project leader on multiple projects, interacts with clients, reviews and evaluates data, writes reports and protocols. Responsible for the scientific conduct of the project and communication of regulatory issues with senior level team members. A day in the Life: <ul><li>Independently performs method validations, method transfers and analytical testing of pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods and protocols applicable to assigned tasks. Designs and drives experiments with minimal supervision.</li><li>Prepares study protocols, project status reports, final study reports and other project-related technical documents.</li><li>Communicates data and technical issues to the client and responds to client needs and questions.</li><li>Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instrument and analytical problems.</li><li>Assists with quality systems and new equipment.</li><li>Assists in designing method validation or method transfer protocols and establish project timelines.</li><li>Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.</li></ul> Keys to Success: Education <ul><li>Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li></ul> Experience <ul><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 6+ years).</li><li>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</li></ul> Knowledge, Skills, Abilities <ul><li>Solid understanding and knowledge of general chemistry and separation science</li><li>Experience with Protein Characterization</li><li>Experience with Proteomics</li><li>Mass Spectrometry experience</li><li>LCMS experience</li><li>Orbitrap experience</li><li>Full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance</li><li>Ability to apply Microsoft Excel and Word to perform tasks</li><li>Proficiency on technical operating systems</li><li>Proven problem solving and troubleshooting abilities</li><li>Effective oral and written communication skills</li><li>Proven ability in technical writing skills</li><li>Time management and project management skills</li><li>Ability to work in a collaborative work environment with a team</li><li>Proven problem solving and troubleshooting abilities</li><li>Ability to train junior staff</li></ul> Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: <ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds.</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul>

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Cell Department Middleton, Wisconsin, United States of America Job Description 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+ 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. Discover Impactful Work: Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence. Performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. Enters data into databases and reports. Performs self-review for own data prior to QC submission. A Day in the Life: <ul><li>Support late phase or commercial client on release and stability projects.</li><li>Protocol and method generation, technical support to the team, client communications, nonconformance writing and leading OOS investigations.</li><li>Works with multiple functional groups to meet business needs.</li><li>Plans and organizes work with periodic supervision.</li><li>Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).</li><li>Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.</li></ul> Qualifications - External Keys to Success: Education MS degree with 5+ years of experience; BS degree with 6+ years of experience. Experience <ul><li>Laboratory experience involving cell culture, cell bioassay, PCR</li><li>Experience with Release and Stability programs.</li><li>Prior client interfacing experience needed.</li><li>Experience delivering project completion to timeline.</li><li>Teamwork: data sharing, problem-solving, and collaborating.</li></ul> Knowledge, Skills, Abilities <ul><li>Proficient in Microsoft Excel and Word</li><li>Proven ability to interpret data by performing trend analysis</li><li>Proven ability in technical writing skills</li><li>Ability to independently optimize analytical methods</li><li>Proven problem solving and troubleshooting abilities</li><li>Good written and oral communication skills</li><li>Time management and project management skills</li><li>Ability to work in a collaborative work environment with a team</li></ul><ul><li>Skilled at written and verbal communication, documenting and sharing experimental methods, data, outcomes, and conclusions to diverse audiences.</li><li>Ability to identify issues and adapt experiments on-the-fly, a skill facilitated by strong attention to detail and a willingness to ask for help.</li><li>Skilled at prioritization and navigating ambiguity with a positive demeanor.</li></ul> Work Environment Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: <ul><li>Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>Able to work upright and stationary and/or standing for typical working hours.</li><li>Able to lift and move objects up to 25 pounds.</li><li>Able to work in non-traditional work environments.</li><li>Able to use and learn standard office equipment and technology with proficiency.</li><li>May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.</li><li>Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li></ul> Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status

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Research Scientist Thermo Fisher Scientific Jobs

Research Scientist Large Molecule LcmsJuly 16, 2024

Associate Research ScientistJuly 5, 2024

Research Scientist Cell BioassayJuly 2, 2024

Assoc Research Scientist Analytical ChemistryJuly 1, 2024

Directorsenior Research Scientist Health Economic Modelling EvideraJuly 1, 2024

Associate Research Scientist LcmsJune 28, 2024

Associate Research Scientist Cell Based BioassayJune 28, 2024