Sr Site Specialist
at Thermo Fisher Scientific
Remote, Maluku Utara, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Oct, 2024 | Not Specified | 31 Jul, 2024 | N/A | Teams,Communication Skills | No | No |
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Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION
Thermo Fisher Scientific is the world leader in serving science! We enable our customers to make the world healthier, cleaner, and safer by providing analytical instruments, equipment, reagents and consumables, software and services for research, analysis, discovery and diagnostics. With annual sales of $17 billion, we have over 50,000 employees and serve more than 350,000 customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries.
POSITION SUMMARY:
The position is in the Global Product Stewardship (GPS) team.
The candidate must have some chemical knowledge so as to allow better understanding of the products regulatory and registration based on
GPS requirements. Specialist must have a keen eye for details, systematic and be able to perform tasks based on formalized procedures.
QUALIFICATIONS AND CRITERIA
- Possess a Diploma in Science or related field.
- Able to work independently, multitask and perform in a dynamic environment and meeting specific tight deadline.
- Detail oriented, meticulous and systematic
- Effective business communication skills, both verbal and written
- Strong interpersonal and communication skills to establish working relationship with people from different cultures and levels, both internally and externally
- Being a great teammate to the team and highly skilled to work constructively in teams under time pressure
- Proficient in Microsoft Office suite (i.e. Excel and Word); willingness to learn new software tools
Responsibilities:
Competently support various regulatory and registration work required for GDMA.
Process, post and retrieve required data to and from the database system.
Perform cross-training to other Specialists when required.
Gain direction from Team Leader/Supervisor on work assignments.
Conduct all assigned work to meet the compliance with organization’s safety and quality requirements.
Communicate operation issues to Team Leader.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Diploma
Proficient
1
Remote, Singapore