
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
🔥 1 minute ago
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10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Assists in the coordination and preparation of basic scientific documents under direct supervision • Responsible for preparing and editing scientific documents to meet or exceed quality standards • Assists in the design, preparation and review of analytical protocols for validation or analytical studies • Prepares and/or assists in the preparation of scientific documents such as next time point creates or other basic shell creation • Ensures that hardcopy and electronic reports are consistent and comply with required formats • Reviews data tables and listings and ensures that errors are corrected • Edits and performs a quality control review of scientific documents prior to creation of the final pdf deliverable • Ensures compliance with PPD, Client, eCTD policy and procedure on publications • Reviews technical documents for accuracy, formatting, consistency and compliance to protocols or SOPs • May represent the laboratory on project teams and update team members on the status of study reports • Acts as a liaison on interdepartmental projects when reports are required • Keeps updated on the guidelines and requirements of the FDA and other international regulatory agencies for reference in the development of required documents • May help write Training Materials Documents and Standard Operating Procedures related to Scientific Writing functions • Works with more senior staff on approach for new assignments • Performs other duties as assigned
• Bachelor’s degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years) or equivalent combination of education, training, & experience • Working knowledge of scientific terminology, medical, pharmaceutical and research concepts • Knowledge of word processing, spreadsheets, table and graph generation • Effective written and oral communication skills • Detail oriented • Computer skills including Microsoft Office • Time management skills • Good editorial and proofreading skills • Problem solving and troubleshooting skills • Ability to work well in a collaborative team environment
• Health and wellbeing support • Healthy work-life balance
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