Job Description
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
A Day in the Life:
• Incoming goods inspection with inspection and release of the raw materials
• Outgoing goods inspection: Final inspection of packaged study medication ready for shipment / customer-specific shipments
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• Processing of dispensing/sampling requests
• Incoming goods inspection with inspection and release of the raw materials
• Outgoing goods inspection: Final inspection of packaged study medication ready for shipment / customer-specific shipments
• Processing of dispensing/sampling requests
• Prevention measures against quality deviations
• Execution / monitoring of tool operations
• Storage of sample trains
• Monitoring the destruction of bulk material, study medication, packaging material
• Collaboration in the creation/revision of SOP's and WIs
• Identification of personal training needs
• Participation in regular coordination meetings
• Informing direct superiors about fundamental and significant difficulties
• In quarantine or blocking of materials
• Organization for the execution of sample trains
• Data collection for evaluation of KPIs
• Participation in cross-departmental meetings
• Processing of customer-specific inspection criteria
• Carrying out weekly inspection rounds in the warehouse
• Organization, implementation and processing of deviations
Minimum Requirements / Qualifications:
Qualifications & Experience
- Bachelor of Science (Biotechnology, Chemistry, or closely related degree). Background in analytical theory and technical competency with laboratory analysis. Knowledgeable with cGMP and various laboratory analyses, efficient sample workflows, in process controls, analytical testing and equipment maintenance/introduction.
- Ability to effectively communicate in multiple modalities (e.g. electronic, written, verbal, etc.), Good knowledge of Microsoft applications (e.g. Excel, Word, Outlook, PowerPoint).
- Ability to work on multiple projects simultaneously.
- Strong team-working and collaborative skills. Previous experience in leadership and personnel management-desirable
Skills & Attributes
- Adaptability: Ability to adapt to day to day business requirements.
- Collaborating: Demonstrates the ability to work with all departments and colleagues of varied backgrounds.
- Continuous Improvement: Demonstrates the ability to challenge the status quo to drive PPI.
- Customer Focus: Demonstrates the ability to deliver on promises made to customers i.e. meet agreed due dates.
- Initiating Action: Demonstrates the ability to work independently, and manage planned work. Ability to work on multiple projects or tasks simultaneously.
- Quality Orientation: Ability to interpret and apply cGMP principles, strong attention to detail and accurate completion of test records. Strives for right first time in every task undertaken.
Other Job Requirements:
Deliver the best technical and scientific solutions to improve product value. Build a culture of engagement, accountability and a shared commitment to excellence. Abide by all EH&S policies and procedures, operate our business in a safe, focused, responsible, and ethical fashion. Work safely and only perform tasks if currently competent and/or authorised, participate in EH&S activities such as; GEMBA walks, inspections, and risk assessments.
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.