📑 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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📑 Technical Writer (IT Network Documentation) 6+ MonthsJersey City, NJ – HybridOverview: We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in IT Network Documentation, you will be responsib ...
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📑 Technical Writer (IT Network Documentation) Make sure to read the full description below, and please apply immediately if you are confident you meet all the requirements. 6+ Months Jersey City, NJ – Hybrid Overview: We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in ...
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📑 Technical Writer (IT Network Documentation) 6+ Months Jersey City, NJ Hybrid Overview: We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in IT Network Documentation, you will be responsible for creating clear, concise, and accurate documentation for our network infrast ...
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📑 Technical Writer (IT Network Documentation) 6+ MonthsJersey City, NJ – HybridOverview: We are seeking a talented Technical Writer to join our team at a leading financial institution. As a Technical Writer specializing in IT Network Documentation, you will be responsible for creating clear, concise, and accurate documentation for our network infrast ...
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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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📑 **Scientist / Engineer II Pilot Process Development (Downstream)**Redwood City, CA / Technology Development Manufacturing Sciences & Technology / Full Time Adverum is looking for a Scientist/Engineer II, Pilot Process Development (PPD), Downstream, to join the Manufacturing Sciences and Technology (MSAT) team at our Redwood City, CA office. This ...
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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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📑 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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📑 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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📑 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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📑 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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📑 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 developmen ...
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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, cre ...
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📑 Sizable and reputable hedge fund in New York seeks Equities Analyst/Associate to support senior members of biotech investment team. Firm's partner led group covers both public and private biotech companies research and investments.Among this multi-strategies fund's top operations, this team's investments in biotech/healthcare domain range from mid ...
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📑 A clinical-stage biotech focused on Rare Diseases. This company utilizes antibodies to harness the bodies immune system to fight off disease.The RoleThis person ill serve as the GRL for the company's early stage proprietary pipeline as well as supporting partnered programs with large pharma , reporting into the SVP of Regulatory Affairs.Main Respon ...
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📑 Do you want more than just another job? Are you ready to team up with an organization that values your contributions? Then Hired by Matrix is for you!Working with some of the US' premier companies, we excel at connecting candidates with positive cultures and dynamic teams. We even go the extra mile with our signature Consultant ...
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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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📑 Job Summary: We are seeking a dedicated and experienced Laboratory Manager to oversee laboratory operations in a Biotech company located in Redwood City, California. The Laboratory Manager will play a critical role in ensuring the smooth functioning of our research and development laboratories, supporting innovative projects aimed at advancing nove ...
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📑 Job Summary: We are seeking a dedicated and experienced Laboratory Manager to oversee laboratory operations in a Biotech company located in Redwood City, California. The Laboratory Manager will play a critical role in ensuring the smooth functioning of our research and development laboratories, supporting innovative projects aimed at advancing nove ...
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📑 Cellino is building a precision platform that personalizes human cells for all. Stem cell-derived regenerative medicines are poised to cure some of the toughest diseases within this decade, including Parkinson’s, diabetes, and heart disease. Patient-specific cells provide the safest, most effective cures for these indications. Currently, large scal ...
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📑 We are seeking highly motivated and experienced IT Finance Coordinator to join our top biotech client's dynamic IT Portfolio Ops team.Responsibilities:* Coordinate all aspects of assigned IT projects within the Global IT Ops portfolio, ensuring adherence to established timelines, budgets, and quality standards.* Facilitate effec ...
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📑 Sales reps that do best: motivated and personable people that can do 30-50 store visits weekly. Bartenders, car sales, service reps from other industries are all good fits! Can be your full time job or compliment people that have hourly jobs at night or on the weekend while they build their sales network. This is a commission only job and will take ...
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📑 Sales reps that do best: motivated and personable people that can do 30-50 store visits weekly. Bartenders, car sales, service reps from other industries are all good fits! Can be your full time job or compliment people that have hourly jobs at night or on the weekend while they build their sales network. This is a commission only job and will take ...
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📑 Sales reps that do best: motivated and personable people that can do 30-50 store visits weekly. Bartenders, car sales, service reps from other industries are all good fits! Can be your full time job or compliment people that have hourly jobs at night or on the weekend while they build their sales network. This is a commission only job and will take ...
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📑 Sales reps that do best: motivated and personable people that can do 30-50 store visits weekly. Bartenders, car sales, service reps from other industries are all good fits! Can be your full time job or compliment people that have hourly jobs at night or on the weekend while they build their sales network. This is a commission only job and will take ...
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📑 Tlando Therapeutic SpecialistVerity Pharmaceuticals, an emergent privately owned healthcare company actively promoting products in the US and Canada, is seeking Therapeutic Specialists for our US testosterone replacement therapy business. We are looking for candidates who want to break into Pharmaceutical sales or have had a couple years of experie ...
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📑 Marex is a diversified global financial services platform, providing essential liquidity, market access and infrastructure services to clients in the energy, commodities and financial markets. The Group provides comprehensive breadth and depth of coverage across four core services: Market Making, Clearing, Hedging and Investment Solutions and Agenc ...
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📑 1st Shift: Track and review change control documentation. Assist with the editing of quality documents (SOPs, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements. Must be able to work quickly with a high degree of accuracy. Must possess sound interpersonal and information gathering skills, be able to relate w ...
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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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📑 Location New York City, NY, United States Posted on Jan 12, 2024 Valid Through Feb 11, 2024 ProfileJob OverviewA law firm in New York City is currently seeking a dynamic and qualified Biotech Patent Associate Attorney with a Ph.D. in biochemistry, molecular biology, or immunology. The ideal candidate should possess 0-3 years of patent prosecution e ...
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Great News! We have discovered exciting live Documentation biotech job opportunities in Jersey city just for you at American Jobs. You can even download the search results for Documentation biotech jobs in jersey city here.
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There are currently 8000 live jobs available for Documentation biotech in Jersey city according to American Jobs.
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There are currently 2,120,215 total jobs available in United States according to American Jobs.