QC Chemist I (12 hrs shift)
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Job Location:
Monthly Salary:
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob Description
Be part of our Quality Control team at Thermo Fisher Scientific where youll contribute by ensuring the quality and reliability of products that help make the world healthier cleaner and safer. Youll perform testing and analysis to support the development of innovative therapeutic products. Youll conduct quality control testing of raw materials in-process samples and finished products using various analytical techniques. Youll document and analyze test results participate in investigations and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.
Responsibilities
* To perform QC testing of raw materials incoming goods intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.
* To perform and coordinate monitoring calibration and maintenance of laboratory equipment.
* To lead the preparation of technical documentations such as protocols position papers and risks assessments.
* To perform write up for laboratory investigations deviation and on time closure in line with Quality Management system procedures. (if required)
* To support method transfer/verification/validation for new product introduction.
* To perform periodic reviews for laboratory documents.
* To manage QC chemicals and consumables inventory stock check.
* To maintain the accuracy completeness and compliance of laboratory data.
* To participate in continuous improvement activities.
* To maintain own training records.
* To communicate effectively with others on site and internationally and to participate with them in problem solving activities.
* To ensure cGMP is applied and adhered to in their area of work.
* To support shift work (if necessary).
* Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab.
* Support and encourage a Quality Culture and company 4i values throughout QC.
* Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.
* To work with HSE cGMP and 5S in mind at all times.
* Undertake ad-hoc activities that may be required by the business.
Knowledge Skills Abilities:
* Ability to work independently and adhere to critical timelines.
* Effective communication skills at all internal and external levels.
* Excellent attention to detail.
* Excellent organizational skills.
* Strong in analytical skill and problem-solving skills.
Preferred Experience and Skills:
* Degree in Chemistry or strongly related scientific discipline.
* At least 2-3 years relevant industrial experience.
* Ability to apply GMP regulations and other international guidelines to all aspects of the position.
* Ability to work independently and adhere to critical timelines.
Required Experience:
IC
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
