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QC Scientist I
2 weeks ago
Work Schedule
First Shift (Days)Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materialsJob Description
Job DescriptionWhen you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment and speeding up the manufacturing of treatments for various products. Your work will have real-world impact for patients that are waiting for life-saving medicines, and you will be supported in achieving your career goals
How you will make an impact:You enjoy working with people. You are collaborative, upbeat and optimistic. You are passionate about science, eager to learn and develop your career in the biotech industry. As a member of the operations team, you will play a crucial role in ensuring the integrity and accuracy of our quality control processes. With our commitment to excellence for our customers, you will have the chance to independently perform routine and non-routine testing, covering various areas such as raw materials, in-process products, final products, stability, and validation. Your expertise in analyzing test data, evaluating results, and drawing insightful conclusions will be invaluable.
You must be able to multi-task in a fast-paced environment, quickly addressing day-to-day issues and yet remain focused on prioritized tasks. Excellent organization, time management, and communication skills are essential. A self-motivated individual that is detail-oriented and can function both independently as well as part of a team is required.
Responsibilities Include:- Perform manual calculation of data, sampling and sample preparation procedures, solution preparations, and work done using both validated and unvalidated test methods.
- Review data collected and results derived from other laboratory instrumentation such as UV spectrometers, Charles River LAL assay, Owl cast gel rig as well as data recorded by observation or other physical testing.
- Work closely with operations and quality to ensure final product meets customers specification
- Review results entered LIMS system, ensuring they match the data contained in the analysis performed and that they fall within established trends and specifications.
- Maintain inventory for laboratory.
- Notifies Data Review supervisor, or other appropriate supervisor, when unusual or out-of-the-ordinary data results are observed.
- As a member of the Team, you will review work in laboratory notebooks for completeness, correctness, and adherence to all SOP's regarding laboratory notebook procedures and good documentation practices.
- Bachelors Degree (Chemistry or Biology, preferred)
- Minimum 3 years prior laboratory experience
An equivalent combination of education, training, and relevant work experience will be considered.
Knowledge, Skills, Abilities:- Experience with bacterial culture growth, plasmid purification, gel electrophoresis, and working with various assays.
- Solid understand of analytical chemistry (HPLC, Spectroscopy, Dissolution) and documentation requirements.
- Ability to work independently and meet deadlines.
- Organizational and interpersonal skills, including strong oral and written communication skills, and the ability to multi-task and adjust to changing priorities.
- Comfortable working with Microsoft Office
At Thermo Fisher Scientific, each one of our 75,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.
Apply todayThermo 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
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