Scientist - Sample Managment

at  Thermo Fisher Scientific

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.
Thermo Fisher’s clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.
Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to maximise the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

EDUCATION AND EXPERIENCE:

• Bachelor’s degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar
• Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’)
• OR Masters degree
  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:

• Knowledge of applicable regulatory authority and ICH guidelines
• Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation an instrument use
• Ability to apply Microsoft Excel and Word to perform tasks
• Empower software a plus
• Ability to independently optimize analytical methods
• Good written and oral communication skills
• Time management and project management skills
• Problem solving and troubleshooting abilities
• Ability to work in a collaborative work environment with a team
• Strong organization, attention to detail, and multi-tasking skills

• Works with multiple functional groups to meet business needs.
• Plans and organizes work with periodic supervision.
• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
• Ensures QA findings are addressed appropriately.
• Aids and training to other team members.
• Problem solving, either independently or with assistance Communicates project status to project leader.
• Performs work assignments accurately, and in a timely and safe manner.
• Experience in a fast-paced GMP environment
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements
• Understands, implement and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements
• Perform lab support activities as necessary and provide support for department
• Accepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives
• Support investigations