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📑 Job: Validation Lead (CSV, Clinical Systems) Location: NJ/PA(Hybrid) Mandatory Skills: CSV, Computer System Validation, Clinical Systems, periodic review and audit experience Roles and Responsibilities: We are looking for a pure validation resource 8 + years Experience in Validating GxP applications Experience in FDA and/or Global regulated environ ...

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📑 We've partnered with a highly innovative biotech in the proteomics space that is seeking a Scientist, Mass Spectrometry to join the team. This role will be heavily focused on implementing and developing new methods utilizing proprietary technology and will collaborate closely with the data science team as well as other cross-functional groups.Respo ...

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📑 We've partnered with a highly innovative biotech in the proteomics space that is seeking a Scientist, Mass Spectrometry to join the team. This role will be heavily focused on implementing and developing new methods utilizing proprietary technology and will collaborate closely with the data science team as well as other cross-functional groups.Respo ...

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📑 We've partnered with a highly innovative biotech in the proteomics space that is seeking a Scientist, Mass Spectrometry to join the team. This role will be heavily focused on implementing and developing new methods utilizing proprietary technology and will collaborate closely with the data science team as well as other cross-functional groups.</ ...

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📑 Job Title: Syncade Recipe AuthorLocation: RemoteDuration: FulltimeJob Description:Technical/Functional SkillsExperience in Troubleshooting & Resolving issues related to SyncadeMES.Working knowledge of IT Life Cycle management, IT ...

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📑 Responsibilities : PM with strong functional knowledge of Validation and QA for pharmaceutical or biotech. SAP S/4 implementation experience. Able to effectively communicate to business partners across all levels all the way up to leadership (not technical speak). Able to work in a chaotic, high-pressure env ...

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📑 Job Description: The Benchtop Support specialist position will be responsible for providing IT support in our Digital Plant organization working to support, enhance, and maintain compliance for the GxP benchtop systems and instrumentation as well as site and global applications used within the manufacturing, quality, ...

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📑 Responsibilities : PM with strong functional knowledge of Validation and QA for pharmaceutical or biotech. SAP S/4 implementation experience. Able to effectively communicate to business partners across all levels all the way up to leadership (not technical speak). <b ...

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📑 Job DescriptionThe PositionThe Senior Specialist Medical Device and Combination Product (MDCP) engineer is a key technical leader of regulatory and quality system requirements within Organon. Under general direction, the engineer leverages experience gained on scientific/technical/business issues to support project teams and other technical staff i ...

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📑 Responsibilities: Performs a wide variety of activities to ensure compliance with applicable quality objectives and regulatory requirements. Serves as Analytical Operation Lead for clinical and commercial projects. Leads quality investigations/deviations/quality event escalation meetings, and effectively communicate ...

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📑 Associate Director / Senior Manager, Quality AssuranceAllakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammatory and proliferative diseases.Allakos is committed to developing innovative therapies that transform patients' lives. We are ...

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📑 Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, ...

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📑 Due to the company’s expansive portfolio growth, the Evolved By Nature Discovery, Research and Development team is seeking a Scientist to become part of our forward-thinking scientific team. In this role, you will develop novel analytical tools to characterize silk proteins and derivative materials, facilitating their application across a broad spe ...

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📑 100% onsiteNormal business hoursPosition SummaryThis position will directly support qualification and operational activities for the Reference Standard and Critical Reagent (RSCR) Group within the Global Quality Analytical Science & Technology (GQAST) organization. The primary role will fu ...

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📑 Job DescriptionThe PositionThe Senior Specialist Medical Device and Combination Product (MDCP) engineer is a key technical leader of regulatory and quality system requirements within Organon. Under general direction, the engineer leverages experience gained on scientific/technical/business issues to support project teams and other technical staff i ...

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📑 Job Description: The Project Manager, WW Hematology Medical, is responsible for providing logistical and tactical support for assigned projects across different Hematology Disease Areas. He/she collaborates with the Therapeutic Area Leaders and product leads to ensure implementation and execution of project activities ...

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📑 Mitsubishi Chemical Group Director, Government Accounts Jersey City , New Jersey Apply Now Entrepreneurial Spirit, Rooted in Tradition . Mitsubishi Tanabe Pharma America, Inc. (MTPA) is a U.S. subsidiary of Mitsubishi Tanabe Pharma Corporation (MTPC) in Japan, which touts a storied reputation more than 300 years in the making. Our par ...

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📑 Senior Specialist, Quality AssuranceAllakos Inc. is a clinical-stage company developing therapeutic antibodies for inhibitory receptors on the surface of immune effector cells involved in allergic, inflammatory and proliferative diseases.Allakos is committed to developing innovative therapies that transform patients' lives. We are looking for brigh ...

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📑 Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.<s ...

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📑 Job Description:What is the Opportunity?Provide independent and objective evaluation of the adequacy and effectiveness of U.S. Finance and Corporate Treasury (e.g., IRRBB, Liquidity, FTP) and our client's US branches and will support the Director for U.S. Finance and Corporate Treasury with effective audit planning, testing, reporting and issue rem ...

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📑 Responsibilities: Performs a wide variety of activities to ensure compliance with applicable quality objectives and regulatory requirements. Serves as Analytical Operation Lead for clinical and commercial projects. Leads quality investigations/deviations/quality event escalatio ...

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📑 We are seeking a talented and motivated Manufacturing Scientist/Engineer to join a Biotech company located in Redwood City. The ideal candidate will play a pivotal role in the development and optimization of manufacturing processes. This position offers an exciting opportunity to contribute to the advancement of cutting-edge treatments aimed at imp ...

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📑 We are seeking a talented and motivated Manufacturing Scientist/Engineer to join a Biotech company located in Redwood City. The ideal candidate will play a pivotal role in the development and optimization of manufacturing processes. This position offers an exciting opportunity to contribute to the advancement of cutting-edge treatments aimed at imp ...

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📑 Senior Research Associate II, Analytical Development and Operations page is loaded Senior Research Associate II, Analytical Development and Operations Apply locations United States - California - Foster City time type Full time posted on Posted 3 Days Ago job requisition id R0040170 For Cu ...

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📑 Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.ResponsibilitiesProvide ...

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📑 Job Description:What is the Opportunity?Provide independent and objective evaluation of the adequacy and effectiveness of U.S. Finance and Corporate Treasury (e.g., IRRBB, Liquidity, FTP) and our client's US branches and will support the Director for U.S. Finance and Corporate Tre ...

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📑 Overview:Entrepreneurial Spirit, Rooted in Tradition. Mitsubishi Tanabe Pharma America, Inc. (MTPA) is a U.S. subsidiary of Mitsubishi Tanabe Pharma Corporation (MTPC) in Japan, which touts a storied reputation more than 300 years in the making. Our parent company - one of Japans most respected - is a research-driven pharmaceutical company that has ...

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📑 Northreach is a dynamic recruitment agency that connects businesses with top talent in the Advanced Therapies sector. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth.<s ...

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📑 W2 only - No C2C Must Have: Heavy risk background, Erwin, Data Modeling, AWS CloudData authority, data use cases, great communication skills, Data AccessData initiative for corporate risk space, market risk, Corporate risk driven architecture space. Job Description:Highly proficient in data architecture disciplines with proficiency in the other dis ...

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📑 MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development m ...

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📑 MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creati ...

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📑 MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development m ...

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📑 Summary Reports, Change Controls. • Manages projects of varying scope and complexity. • Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area. • Independent ownership of all lif ...

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