Technical Trainer Salary at Bjit Inc BETA

OPPORTUNITY Mammoth is seeking an experienced and highly motivated Director of Drug Product Development - Sterile Products (mRNA Therapeutics) to lead formulation and process development for our pipeline of mRNA-based therapeutics. This is a critical and hands-on leadership role within a start-up environment. The successful candidate will be responsible for establishing the sterile drug product development function, working cross-functionally to support early-phase development through clinical supply, and partnering with external manufacturing organizations to bring first-in-human and subsequent programs to the clinic. KEY RESPONSIBILITIES Strategic & Functional Leadership: Serve as the drug product subject matter expert for mRNA-LNP sterile injectables, establishing internal capabilities and setting phase-appropriate development strategies Build the drug product development function from the ground up-designing systems, workflows, and documentation standards suitable for an early-stag

Job Title: Software Development Manager - Control Plane Workplace Type: Hybrid, 3 days per week (San Jose, CA) About Us: Index Engines is the world’s leading AI powered analytics engine to detect data corruption due to ransomware. The company’s CyberSense® product empowers organizations to detect ransomware and data corruption and facilitate rapid recovery from attacks. CyberSense is the last line of defense for thousands of organizations worldwide. The Index Engines Engineering team uses the Scrum Agile methodology. The Engineering Team is distributed across four geographic locations: Holmdel NJ, San Jose CA, Colorado Springs CO, and Pune India. Role Overview: Index Engines uses the Agile Scrum methodology. This individual will lead software engineers assigned to work on Scrum Teams. The software application runs on the Linux operating system and is primarily written in the C-Language, with some code written in Python. This individual will: Lead and manage a growing team of 10+ softwa

Kelly® Science & Clinical is seeking a Senior Quality Specialist for a two-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and diagnostics industries. Workplace: Onsite in Sunnyvale, CA Position Title: Senior Quality Specialist Position Type: Two-year contract Pay rate: $65-80/ hour. Company: Kelly® Science & Clinical Overview The Senior Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle Quality group in R&D and reports to the Sr. Manager, Product Lifecyle Quality, and will be onsite based, located in Sunnyvale, California. R

Kelly® Science & Clinical is seeking a Senior Quality Specialist for a two-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and diagnostics industries. Workplace: Onsite in Sunnyvale, CA Position Title: Senior Quality Specialist Position Type: Two-year contract Pay rate: $65-80/ hour. Company: Kelly® Science & Clinical Overview The Senior Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle Quality group in R&D and reports to the Sr. Manager, Product Lifecyle Quality, and will be onsite based, located in Sunnyvale, California. R

Kelly® Science & Clinical is seeking a Senior Quality Specialist for a two-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and diagnostics industries. Workplace: Onsite in Sunnyvale, CA Position Title: Senior Quality Specialist Position Type: Two-year contract Pay rate: $65-80/ hour. Company: Kelly® Science & Clinical Overview The Senior Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle Quality group in R&D and reports to the Sr. Manager, Product Lifecyle Quality, and will be onsite based, located in Sunnyvale, California. R

Kelly® Science & Clinical is seeking a Senior Quality Specialist for a two-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and diagnostics industries. Workplace: Onsite in Sunnyvale, CA Position Title: Senior Quality Specialist Position Type: Two-year contract Pay rate: $65-80/ hour. Company: Kelly® Science & Clinical Overview The Senior Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle Quality group in R&D and reports to the Sr. Manager, Product Lifecyle Quality, and will be onsite based, located in Sunnyvale, California. R

Kelly® Science & Clinical is seeking a Senior Quality Specialist for a two-year contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and diagnostics industries. Workplace: Onsite in Sunnyvale, CA Position Title: Senior Quality Specialist Position Type: Two-year contract Pay rate: $65-80/ hour. Company: Kelly® Science & Clinical Overview The Senior Quality Specialist is responsible for supporting quality systems activities related to assay development, especially, design control and risk management activities in accordance with FDA and ISO regulations. This position is part of the Product Lifecyle Quality group in R&D and reports to the Sr. Manager, Product Lifecyle Quality, and will be onsite based, located in Sunnyvale, California. R

**General Description:** + The Senior Manager, Regulatory Affairs CMC, is responsible for developing and implementing global regulatory CMC strategies to secure and maintain market access for assigned product(s) in line with business objectives, and in coordination with key internal stakeholders. This position will manage regulatory CMC aspects of compounds (large molecules) through all phases of development, post-approval, and life cycle of the product depending on assigned products. Primary responsibilities will be in creating CMC regulatory strategies for development programs in preparation and maintenance of regulatory applications **Essential Functions of the Job:** + Serve as the regulatory CMC representative on project teams. Provides CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues, as well as third party laboratories, global collaborations partners and contract manufacturers