Thermo Fisher Scientific Jobs overseas

About 3467 results in (2) seconds Clear Filters

Jobs Search

Experienced Clinical Research Associate (FSP) (CRA II / Senior CRA)- Quebec at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Montreal, Quebec, Canada - Full Time

Skills Needed
Clinical Monitoring, Site Management, Regulatory Compliance, Risk Based Monitoring, Critical Thinking, Problem Solving, Data Accuracy, Communication Skills, Interpersonal Skills, Attention To Detail, Organizational Skills, Time Management, Microsoft Office, Bilingual, Neurology

Specialization
Candidates must have a bachelor's degree in a life sciences field or equivalent, along with CRA experience in neurology and bilingual proficiency in French and English. A valid driver's license is required, and a minimum of 2 years of relevant experience is preferred.

Experience Required
Minimum 2 year(s)

Director, Digital Manufacturing IT at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Hyderabad, Telangana, India - Full Time

Skills Needed
Digital Manufacturing Strategy, Cmms, Mes, Shop Floor Integration, Regulatory Compliance, Project Management, Team Leadership, Operational Excellence, Data Driven Insights, Continuous Improvement, Predictive Maintenance, Real Time Monitoring, Automation, Industry 4.0 Technologies, Iot, Analytics

Specialization
Candidates should have a bachelor's or master's degree in a relevant field and at least 10 years of experience in manufacturing IT, preferably in the pharmaceutical sector. Expertise in CMMS, MES, and regulatory compliance is essential.

Experience Required
Minimum 10 year(s)

HR Generalist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Melbourne, Victoria, Australia - Full Time

Skills Needed
Employee Relations, Talent Acquisition, Performance Development, Organisational Planning, Compensation Planning, Succession Planning, Data Integrity, Hris, Problem Solving, Collaboration, Learning Agility, Resilience, Confidentiality, Employee Engagement, Performance Improvement, Hr Projects

Specialization
Candidates should have an undergraduate degree in Business, Psychology, or HR, along with 3-5 years of relevant HR experience. Proven knowledge in various HR aspects and proficiency in MS Office tools are also required.

Experience Required
Minimum 2 year(s)

Associate Clinical Sample Coordinator - 5 Days Work (Morning or Late Shift) at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Singapore, , Singapore - Full Time

Skills Needed
Microsoft Office, Time Management, Documentation, Communication, Team Collaboration

Specialization
A high school diploma or equivalent is required, along with previous experience that provides the necessary knowledge and skills. Familiarity with Microsoft Office and strong time management skills are also important.

Sales Development Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Shanghai, Shanghai, China - Full Time

Skills Needed
Sales Development, Customer Engagement, Communication Skills, Resilience, Self Discipline, Time Management, Goal Oriented, Technical Sales, Bioprocessing, Data Driven Insights, Curiosity, Learning, Collaboration, Follow Up, Market Visibility, Prospect Qualification

Specialization
A Bachelor or Master's degree is required along with 3-5 years of commercial experience in the Bioprocessing industry. Candidates should possess exceptional communication skills and a goal-oriented mindset.

Experience Required
Minimum 2 year(s)

Product Safety Compliance Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Marietta, Ohio, United States - Full Time

Skills Needed
Regulatory Compliance, Project Management, Analytical Reasoning, Interpersonal Skills, Detail Orientation, Manufacturing Processes, Risk Assessment, Technical Documentation, Post Market Surveillance, Quality Assurance, Communication Skills, Team Collaboration, Iso Standards, Product Lifecycle Management, Investigational Curiosity, Ethical Conduct

Specialization
A high school diploma is required, with a suggested bachelor's degree in a relevant field. Candidates should have at least 3 years of experience in quality, compliance, or verification roles, particularly in manufacturing environments.

Experience Required
Minimum 2 year(s)

Sales Team Lead at THERMO FISHER BIOPHARMA SERVICES PTE LTD

, Selangor, Malaysia - Full Time

Skills Needed
Leadership, Sales Management, Customer Relationship Management, Channel Partner Management, Cross Functional Collaboration, Marketing Execution, Market Intelligence, Analytical Skills, Presentation Skills, Negotiation Skills, Solution Selling, Team Development, Forecasting, Product Management, Strategic Planning, Crm Proficiency

Specialization
Candidates should have a Bachelor’s or Master’s degree in a relevant scientific discipline and a minimum of 5 years of experience in chemical and analytical consumables sales. Leadership experience and a strong understanding of the Malaysian market are also required.

Experience Required
Minimum 5 year(s)

Order Support Specialist SME- German speaking at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Budapest, Central Hungary, Hungary - Full Time

Skills Needed
Customer Service, Order Management, Problem Solving, Attention To Detail, Communication Skills, Organizational Skills, Self Motivation, Team Player, Microsoft Office, Multitasking, Technical Skills, Data Accuracy, Process Improvement, Training Development, Customer Relationship Management, Escalation Management

Specialization
Candidates should have 3-5 years of customer service experience in a multinational environment and be proficient with ERP systems. A high school diploma is required, with a preference for a bachelor's degree.

Experience Required
Minimum 2 year(s)

Sales Development Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Shanghai, Shanghai, China - Full Time

Skills Needed
Sales Development, Customer Engagement, Communication Skills, Resilience, Self Discipline, Time Management, Technical Sales, Bioprocessing, Goal Oriented, Curiosity, Learning, Data Driven Insights, Collaboration, Market Visibility, Lead Follow Up, Opportunity Identification

Specialization
Candidates should have a Bachelor or Master's degree and 3-5 years of commercial experience in the Bioprocessing industry. Exceptional communication skills and a goal-oriented mindset are essential for success in this role.

Experience Required
Minimum 2 year(s)

Regulatory Affairs Director at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Seoul, , South Korea - Full Time

Skills Needed
Regulatory Expertise, Communication, Leadership, Customer Engagement, Cross Functional Leadership, Industry Insight

Specialization
Candidates must have extensive experience working at an Asia regulatory authority and a proven track record in regulatory affairs across multiple countries in Asia. Strong communication and leadership skills are essential, along with the ability to engage with customers and work independently.

Experience Required
Minimum 10 year(s)

Scientist III - Technical Project Manager (Biopharmaceuticals) at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Middleton, Wisconsin, United States - Full Time

Skills Needed
Analytical Instrumentation, Biopharmaceutical Methods, Hplc, Ce, Gmp, Documentation, Troubleshooting, Project Management, Time Management, Communication, Problem Solving, Method Optimization, Collaboration, Mentoring, Root Cause Analysis, Quality Assurance

Specialization
A Bachelor's degree or equivalent and at least 5 years of relevant experience are required. Knowledge of analytical instrumentation and biopharmaceutical methods is strongly preferred.

Experience Required
Minimum 5 year(s)

Senior Buyer at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Singapore, , Singapore - Full Time

Skills Needed
Material Requirements Planning, Purchase Order Generation, Supplier Management, Cost Negotiation, Supply Chain Metrics, Material Obsolescence Analysis, Vendor Managed Inventory, Contract Management, Regulatory Compliance, Inventory Auditing, Raw Material Inventory Control, Team Guidance, Problem Solving, Data Analysis, Communication, Negotiation

Specialization
The job requires experience in procurement and supply chain management, with a focus on material planning and supplier negotiations. Familiarity with regulatory standards such as SOX, ISO13485, and FDA regulations is essential.

Experience Required
Minimum 5 year(s)

Validation Scientist Research & Development at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Zaventem, Flemish Brabant, Belgium - Full Time

Skills Needed
Analytical Instrumentation, Sops, Regulatory Guidelines, Sample Preparation, Biopharmaceutical Compounds, Documentation, Problem Solving, Time Management, Project Management, Communication Skills, Collaboration, Quality Control, Manual Dexterity, Troubleshooting, Qa Processes, Cross Training

Specialization
Candidates should possess a bachelor's degree or equivalent and have 0-2 years of relevant experience. Knowledge of analytical instrumentation and regulatory guidelines is essential.

QC Tech II - 1st Shift at THERMO FISHER BIOPHARMA SERVICES PTE LTD

, Virginia, United States - Full Time

Skills Needed
Laboratory Techniques, Quality Processes, Data Analysis, Scientific Reasoning, Troubleshooting, Communication Skills, Interpersonal Skills, Organizational Skills, Prioritization Skills, Cgmp Standards, Glp Standards, Training, Mentoring, Process Improvement, Instrument Management, Sample Preparation

Specialization
Candidates should have an Associate's or Bachelor's degree in a scientific discipline or equivalent experience, along with a minimum of 2 years in a Quality Control laboratory. Strong understanding of laboratory techniques and quality processes is essential.

Experience Required
Minimum 2 year(s)

Trial Activation Approval Specialist II/SSU II at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Beijing, Beijing, China - Full Time

Skills Needed
Regulatory Compliance, Submission Strategy, Project Coordination, Client Communication, Feasibility Activities, Patient Information, Informed Consent, Safety Dossiers, Import License, Gene Therapy Approvals, Internal Communication, Timely Submissions, Issue Resolution, Budget Negotiation, Study File Management, Sop Knowledge

Specialization
The role requires expertise in regulatory processes and the ability to coordinate with various internal departments. Familiarity with PPD SOPs, client directives, and current regulatory guidelines is essential.

Experience Required
Minimum 2 year(s)

Billing & Invoicing Manager at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Sofia, Sofia-City, Bulgaria - Full Time

Skills Needed
Problem Solving, Prioritizing, Accounting Principles, Financial Principles, Analytical Skills, Quantitative Skills, Presentation Skills, Microsoft Office, Communication Skills, Interpersonal Skills, Multi Tasking, Leadership, Coaching, Mentoring

Specialization
Candidates should have 3+ years of leadership experience and a strong background in financial analysis. Proficiency in problem-solving, communication, and team management is essential.

Experience Required
Minimum 2 year(s)

Scientist II - ICP-MS at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Middleton, Wisconsin, United States - Full Time

Skills Needed
Icp, Microsoft Excel, Microsoft Word, Data Interpretation, Technical Writing, Analytical Methods Optimization, Problem Solving, Troubleshooting, Time Management, Project Management, Collaboration, Sample Preparation, Quality Assurance, Regulatory Compliance, Laboratory Procedures, Data Analysis

Specialization
Candidates must have a bachelor's degree or equivalent and at least 2 years of relevant experience. Prior experience with ICP is preferred, along with proficiency in Microsoft Office and strong problem-solving skills.

Experience Required
Minimum 2 year(s)

Distribution Receiving Supervisor at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Florence, Kentucky, United States - Full Time

Skills Needed
Leadership, Supervisory Skills, Coaching, Motivation, Customer Orientation, Problem Solving, Communication, Performance Evaluation, Training, Warehouse Management, Sop Compliance, Team Organization, Process Improvement, Safety Compliance, Inventory Control, Logistics

Specialization
A bachelor's degree in Business Administration, Supply Chain, or a related field is preferred, along with 3-5 years of experience in a distribution center. Candidates must possess leadership skills and the ability to communicate effectively with employees and management.

Experience Required
Minimum 2 year(s)

Record to Report - Systems Accountant at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Quezon City, Metro Manila, Philippines - Full Time

Skills Needed
Financial Master Data, System Governance, User Access Controls, Data Accuracy, Compliance, Process Efficiency, Erp Systems, Financial Reporting Tools, Data Quality Checks, Reconciliation Processes, Process Standardization, Training, Collaboration, Problem Solving, Sox Compliance, Advanced Excel Skills

Specialization
Candidates should have a bachelor's degree in Accounting or Finance and at least 5 years of RTR finance experience, with a minimum of 2 years overseeing financial systems. Knowledge of financial reporting tools and strong hands-on experience with ERP systems is essential.

Experience Required
Minimum 5 year(s)

3D Production Technician I - Weekend at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Logan, Utah, United States - Full Time

Skills Needed
Attention To Detail, Problem Solving, Communication, Manufacturing, Teamwork, Safety Standards, Cleanroom Procedures, Documentation, Equipment Operation, Material Handling, Production Processes, Gmp Compliance, Training, Agility, Ppe Usage, Quality Control

Specialization
A high school diploma or equivalent is required, with no previous work experience necessary. Preferred candidates will have experience in manufacturing or a cGMP environment.

Experienced Clinical Research Associate (FSP) (CRA II / Senior CRA)- Quebec at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Montreal, Quebec, Canada -

Full Time

Start Date

Immediate

Expiry Date

07 Mar, 26

Salary

125000.0

Posted On

07 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Monitoring, Site Management, Regulatory Compliance, Risk-Based Monitoring, Critical Thinking, Problem Solving, Data Accuracy, Communication Skills, Interpersonal Skills, Attention to Detail, Organizational Skills, Time Management, Microsoft Office, Bilingual, Neurology

Industry

Biotechnology Research

Description

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 global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies. This position requires overnight travel either regionally or nationally, dependent on business needs. Discover Impactful Work: Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. A day in the Life: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required. Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials. Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc). Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections. Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner. Contributes to other project work and initiatives for process improvement, as required. Keys to Success: Education Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification. Experience Required a bilingual Sn CRA in Canada; Ontario or Quebec, for FSP resourcing purposes. Must have CRA experience in NEUROLOGY in addition to speaking both French and English. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor). Valid driver's license where applicable. 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: Effective clinical monitoring skills Demonstrated understanding of medical/therapeutic area knowledge and medical terminology Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving Ability to manages Risk Based Monitoring concepts and processes Effective oral and written communication skills, with the ability to communicate effectively with medical personnel Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues Effective interpersonal skills Strong attention to detail Effective organizational and time management skills Ability to remain flexible and adaptable in a wide range of scenarios Ability to work in a team or independently as required Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software Good English language and grammar skills Good presentation skills Work Environment Thermo Fisher Scientific values the health and well-being 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: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary for typical working hours. Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments. This role requires independent travel up to 80%, inclusive of traveling in automobiles, airplanes, and trains. 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. The salary range estimated for this position is $83,000 annually - $125,000 annually. This position will also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. Actual compensation will be confirmed in writing at the time of offer. We offer a comprehensive Total Rewards package that our US colleagues and their families can count on, which generally includes: A choice of national medical and dental plans, and a national vision plan - A wellness program, and valuable health incentive opportunities for company contributions to a Health Reimbursement Accounts (HRAs) or Health Savings Account (HSA) - Tax-advantaged savings and spending accounts and commuter benefits - Employee assistance program - Paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy 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. 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. La maîtrise de la langue anglaise est requise pour garantir une communication et une collaboration efficaces avec les membres de l'équipe et les dirigeants d'entreprise dans divers endroits à travers le monde, y compris aux États-Unis. English language proficiency is required to ensure effective communication and collaboration with team members and business leaders in various locations globally, including the United States. Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell? Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $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 complex analytical challenges, increasing productivity 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 delivers an unrivaled 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. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. 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.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Clinical Research Associate (CRA) will perform and coordinate all aspects of clinical monitoring and site management, ensuring compliance with protocols and regulations. They will conduct remote or on-site visits, manage documentation, and develop relationships with investigational sites.

Experienced Clinical Research Associate (FSP) (CRA II / Senior CRA)- Quebec at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Montreal, Quebec, Canada - Full Time

Experience Required
Minimum 2 year(s)

Director, Digital Manufacturing IT at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Hyderabad, Telangana, India - Full Time

Experience Required
Minimum 10 year(s)

HR Generalist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Melbourne, Victoria, Australia - Full Time

Experience Required
Minimum 2 year(s)

Associate Clinical Sample Coordinator - 5 Days Work (Morning or Late Shift) at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Singapore, , Singapore - Full Time

Skills Needed
Microsoft Office, Time Management, Documentation, Communication, Team Collaboration

Sales Development Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Shanghai, Shanghai, China - Full Time

Experience Required
Minimum 2 year(s)

Product Safety Compliance Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Marietta, Ohio, United States - Full Time

Experience Required
Minimum 2 year(s)

Sales Team Lead at THERMO FISHER BIOPHARMA SERVICES PTE LTD

, Selangor, Malaysia - Full Time

Experience Required
Minimum 5 year(s)

Order Support Specialist SME- German speaking at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Budapest, Central Hungary, Hungary - Full Time

Experience Required
Minimum 2 year(s)

Sales Development Specialist at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Shanghai, Shanghai, China - Full Time

Experience Required
Minimum 2 year(s)

Regulatory Affairs Director at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Seoul, , South Korea - Full Time

Skills Needed
Regulatory Expertise, Communication, Leadership, Customer Engagement, Cross Functional Leadership, Industry Insight

Experience Required
Minimum 10 year(s)

Scientist III - Technical Project Manager (Biopharmaceuticals) at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Middleton, Wisconsin, United States - Full Time

Specialization
A Bachelor's degree or equivalent and at least 5 years of relevant experience are required. Knowledge of analytical instrumentation and biopharmaceutical methods is strongly preferred.

Experience Required
Minimum 5 year(s)

Senior Buyer at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Singapore, , Singapore - Full Time

Experience Required
Minimum 5 year(s)

Validation Scientist Research & Development at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Zaventem, Flemish Brabant, Belgium - Full Time

Specialization
Candidates should possess a bachelor's degree or equivalent and have 0-2 years of relevant experience. Knowledge of analytical instrumentation and regulatory guidelines is essential.

QC Tech II - 1st Shift at THERMO FISHER BIOPHARMA SERVICES PTE LTD

, Virginia, United States - Full Time

Experience Required
Minimum 2 year(s)

Trial Activation Approval Specialist II/SSU II at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Beijing, Beijing, China - Full Time

Experience Required
Minimum 2 year(s)

Billing & Invoicing Manager at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Sofia, Sofia-City, Bulgaria - Full Time

Specialization
Candidates should have 3+ years of leadership experience and a strong background in financial analysis. Proficiency in problem-solving, communication, and team management is essential.

Experience Required
Minimum 2 year(s)

Scientist II - ICP-MS at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Middleton, Wisconsin, United States - Full Time

Experience Required
Minimum 2 year(s)

Distribution Receiving Supervisor at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Florence, Kentucky, United States - Full Time

Experience Required
Minimum 2 year(s)

Record to Report - Systems Accountant at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Quezon City, Metro Manila, Philippines - Full Time

Experience Required
Minimum 5 year(s)

3D Production Technician I - Weekend at THERMO FISHER BIOPHARMA SERVICES PTE LTD

Logan, Utah, United States - Full Time

Specialization
A high school diploma or equivalent is required, with no previous work experience necessary. Preferred candidates will have experience in manufacturing or a cGMP environment.