Work Schedule
Standard (Mon-Fri)Environmental Conditions
Cold Room/Freezers -22degreesF/-6degrees C Laboratory Setting Loud Noises (Equipment/Machinery) Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) WarehouseJob Description
Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue exceeding $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 improving patient diagnostics and therapies or increasing productivity in their laboratories we are here to support them.
How will you make an impact
Technically supports day-to-day operations in the Formulation Filling and/or Freeze Drying areas of the Steriles plant.
Investigates validates and may contribute to new scientific methodologies used to control raw materials production intermediates and final products on projects of moderate scope.
May be involved in pre-clinical clinical and/or post-marketing stages of drug development.
Works on technical/scientific process/product/project activities to execute strategies and technical solutions that meet client needs and expectations.
Assists in the creation of processes and equipment design for clinical scale up and/or registration batches including technology transfer of projects to and from clients.
Evaluates and contributes to the design of manufacturing processes and supports problem solving as necessary within defined procedures and practices.
Makes decisions that involve direct application of technical knowledge.
What will you do
Executes and writes deviation investigations to identify the root causes of departures from standards and to assess product impact.
Implements corrective actions and preventive actions (CAPAs) to eliminate the root causes of deviations.
Monitors processes to proactively mitigate the risks of deviations and process upset situations occurring.
Troubleshoots issues when deviations and/or process upset situations occur.
Implements continuous improvement projects to drive improved process efficiency and efficacy. Writes and manages department Standard Operating Procedures (SOPs) Batch Production Records (BPRs) Training documents Protocols etc. to ensure operational excellence and regulatory compliance.
Contributes to development of methods and processes that meet or exceed the expectations of clients and provides innovation as necessary.
Researches current methodologies. Presents research to internal colleagues and supervisor.
Manages projects at the task level under supervision. May manage projects and timelines at the experiment level.
Assists with implementation of new methodologies and processes.
Reviews analytical test results and works with internal team to analyze results.
Liaises with internal scientific analytical and laboratory functional areas to meet project and team objectives.
Performs all duties in strict compliance with Standard Operating Procedures Good Manufacturing Practices Good Laboratory Practices and Safety guidelines. Maintains the necessary compliance status required by company and facility standards
How will you get here
Education:
Bachelors of Science in Chemistry Biochemistry Biology or related physical science.
Experience:
Typically requires 2 years of scientific experience preferably in life sciences. If advanced degree typically requires no previous related experience.
Equivalency:
Equivalent combinations of education training and relevant work experience may be considered.
Our global team of more than 100000 colleagues 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 and Patheon. For more information please visit .
Required Experience:
IC
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