We have other current jobs related to this field that you can find below
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QC Chemist
4 days ago
San Antonio, United States Kelly Services Full timeQC Chemist – Pharmaceutical Kelly Science & Clinical is currently seeking a QC Chemist for one of our top clients in the San Antonio, TX area. This role will be responsible for laboratory analyses supporting manufacturing. Additional Job Responsibilities: Performs chemical and physical tests required for quality control as testing and evaluation of...
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Organic Chemist
2 weeks ago
San Antonio, United States San Antonio Testing Laboratory, LLC. Full time $50,000 - $60,000Job DescriptionJob DescriptionORGANIC CHEMIST WITH EXPERIENCE IN AN ENVIRONMENTAL LABORATORY SETTING FOR FULL-TIME POSITION IN SAN ANTONIO, TEXAS.Must have previous experience with preparation and analysis of EPA Test Methods 8260, TX-1005, and be familiar with NELAP QA/QC requirements. Only applicants with directly related previous experience will be...
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QC Chemist
1 week ago
San Diego, United States R&D Partners Full time $55,000 - $59,000Job DescriptionJob DescriptionYour main responsibilities as a Research Associate:· Perform analytical testing in support of product development and method validation.· Conduct laboratory tests in compliance with established internal Standard Test Methods (STMs), compendial and vendor/partner supplied methods.· Maintain...
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Bulk Formulation Chemist III
4 weeks ago
San Diego, California, United States GRIFOLS, S.A. Full timeWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...
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Quality Control Chemist
4 weeks ago
San Diego, United States Integrated Resources, Inc ( IRI ) Full timeRole: The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw material, in-process, and finished goods. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products. Duties and Responsibilities: The...
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Quality Control Chemist
4 weeks ago
San Diego, United States Integrated Resources, Inc ( IRI ) Full timeRole: The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw material, in-process, and finished goods. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products. Duties and Responsibilities: The...
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Bulk Formulation Chemist III
4 weeks ago
CA-San Diego, United States GRIFOLS, S.A. Full timetable.MiTabla { max-width: 1020px;!important Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders...
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(Senior) Scientist, Lead Discovery
4 weeks ago
San Francisco, United States Site Therapeutics Full timeSite Therapeutics aims to map—down to the nucleotide—the genetic determinants driving immune cell function in human health and disease and to use that information to develop first-in-class small molecule therapeutics for autoimmune disease. Leveraging technology developed in the Marson Lab at UCSF/Gladstone, we will conduct high-throughput functional...
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(Senior) Scientist, Lead Discovery
4 weeks ago
San Francisco, United States Site Therapeutics Full timeSite Therapeutics aims to map—down to the nucleotide—the genetic determinants driving immune cell function in human health and disease and to use that information to develop first-in-class small molecule therapeutics for autoimmune disease. Leveraging technology developed in the Marson Lab at UCSF/Gladstone, we will conduct high-throughput functional...
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Director, Global Quality Assurance
1 month ago
San Francisco, United States TATCHA Full timeAbout Tatcha: Tatcha is a rapidly growing luxury beauty company with a focus on e-commerce excellence combined with a global retail presence. The company was founded in 2009 by Victoria Tsai to share a highly evolved approach to skincare based on classical Japanese ingredients and rituals that are clinically proven and naturally clean. In a uniquely...
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Director, Global Quality Assurance
4 weeks ago
San Francisco, United States TATCHA Full timeAbout TatchaTatcha is a rapidly growing luxury beauty company with a focus on e-commerce excellence combined with a global retail presence. The company was founded in 2009 by Victoria Tsai to share a highly evolved approach to skincare based on classical Japanese ingredients and rituals that are clinically proven and naturally clean. In a uniquely vertical...
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Director, Global Quality Assurance
4 weeks ago
San Francisco, United States Tatcha, LLC. Full timeSupply Chain & Operations - San Francisco, CA - Full TimeAbout Tatcha:Tatcha is a rapidly growing luxury beauty company with a focus on e-commerce excellence combined with a global retail presence. The company was founded in 2009 by Victoria Tsai to share a highly evolved approach to skincare based on classical Japanese ingredients and rituals that are...
QC Chemist- Nanomedicine
3 months ago
We are hiring a QC Chemistry Scientist to support the growth of our teams. Main areas of responsibilities to include:
– Writing study protocols
– Performing analytical data review
– Stability studies management
– Support OOS and OOT troubleshooting, data analysis and interpretation
– Coordination of analytical transfer and validation with subcontractors
– Subcontractor management
– Actively participating to the overall well-functioning of the QC department activities
You will report into our CMC Expert Manager.
Master degree (Bac+5) in Chemistry
Educational background in the field of nanomedicine is a plus
At least 3 years of professional experience in QC department in Biotechnology / pharmaceutical industry environment, in the development and GMP manufacturing of Medical devices / Drug product. Prior experience in QA department is a plus
– Strong knowledge of GMP environment and regulations (BPF, ICH-Q7, ISO13485, US/EU pharmacopeia, others)
– Strong project management skills required
– Rigorous approach to scientific investigations, with a sense of urgency to achieve ambitious milestones
– Strong team spirit is required to perform this job
– Task and result-oriented
- – Enthusiastic and committed to the overall Sapu project
