Quality Document Control Specialist, Contractor I

Responsibilities:Veeva GxP Documentation and archivalProcessing, Sorting, Organization and archival of on-site GxP archives and digital archivesProjects related to GxP documentationAssist with the administration of GxP trainingRequirements / QualificationsBachelor's degree in Science (preferred)0-2 years experienceAttention to detailhighly organizedEager to...

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company...

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to...

Why Join Intellia? Our goal is to develop transformative genome editing therapies that can positively impact the lives of individuals dealing with severe and life-threatening illnesses. Aside from our scientific work, we embrace our four core principles: One, Explore, Disrupt, Deliver, and firmly believe that you can accomplish more at Intellia. We are fully...

Why Join Intellia?Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to...

QA Specialist - Contract - OnsiteProclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company. This is a contract role located in Cambridge, MA.Skills & Requirements:Specialization in Vaccines - Life science - Bioinformatics - Computer Engineering - Regulatory Requirements in Pharmaceutical...

QA Specialist - Contract - OnsiteProclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company. This is a contract role located in Cambridge, MA.Skills & Requirements:Specialization in Vaccines - Life science - Bioinformatics - Computer Engineering - Regulatory Requirements in Pharmaceutical...

Adecco Healthcare & Life Sciences is seeking a contract Quality Engineer for our Medical Instrumentation partner in Cambridge, MA. The anticipated wage for this position is between $32 and $34. Hourly wage may depend upon experience, education, geographic location, and other factors.Benefit offerings include medical, dental, vision, life insurance,...

Vericel Corporation, a leader in advanced therapies for the sports medicine and severe burn care markets, has an exciting opportunity for a top performing Quality professional looking to join and contribute to a commercial stage company with an established portfolio of unique advanced cell therapies and specialty biologics. Reporting directly to Quality...

About the Business LexisNexis Risk Solutions is the essential partner in the assessment of risk. Within our Business Services vertical, we offer a multitude of solutions focused on helping businesses of all sizes drive higher revenue growth, maximize operational efficiencies, and improve customer experience. Our solutions help our customers solve difficult...

Job DescriptionJob DescriptionAbout KalVista Pharmaceuticals, Inc.KalVista Pharmaceuticals, Inc. ) is focused on the discovery, development, and commercialization of novel, oral therapies for diseases with significant unmet need, with an initial focus on hereditary angioedema (HAE). Listed on the Nasdaq Global Market, our headquarters is located in...

Alphanumeric is seeking a QA Specialist to work the 2nd shift in Cambridge, MA for a client dedicated to enhancing lives through medical and pharmaceutical progress.We are in search of a highly skilled and seasoned Senior QA Specialist to join our vibrant team. In this position, you will oversee the quality assurance process to ensure that our products meet...

job summary: As a Quality Systems Specialist, you will be responsible for providing effective and efficient support to the Quality Management Systems (QMS) team by maintaining compliance with company policies, QMS standards, and local regulations. You will report to the QMS Manager. This position provides the opportunity to work directly with Manufacturing,...

The RoleIn this role, you will function as an internal auditor and will provide clinical quality support related to GCP global regulation and guidelines to Clinical and Research and Development teams. Additionally, the Senior Specialist/Specialist applies established knowledge and experience with GCP regulations, guidelines and local legislation to the...

The RoleIn this role, you will function as an internal auditor and will provide clinical quality support related to GCP global regulation and guidelines to Clinical and Research and Development teams. Additionally, the Senior Specialist/Specialist applies established knowledge and experience with GCP regulations, guidelines and local legislation to the...

POSITION TITLE:QA SpecialistDURATION:1YEARSHIFT:3rd Shift- 11pm - 7am Sunday - Thursday 100% ON SITE We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, ensuring that our products meet both Local and Global quality...

Job Description This exciting new opportunity for an experienced Compliance Specialist who will work closely within the Manufacturing Compliance group to achieve department goals. The Compliance Specialist is also responsible for owning and driving manufacturing compliance improvement through deviation resolution, applied root cause analysis, and the...

MORSE is an innovative, employee-owned, tech company located in Kendall Square in Cambridge, MA specializing in solving multi-disciplinary problems faced by the US National Security Ecosystem. Our specially selected team of engineers, software developers and scientists develop algorithms, software integrated prototypes and solutions for Artificial...

:Job Description: Instrument Support Specialist Job Description Summary We are looking for a highly motivated Instrument Support Specialist to provide critical on-site scientific and operational support as part of a dynamic PerkinElmer lab service team. The role is mainly responsible for supporting Flow Cytometry and FACS equipment and scientists operators...

Senior Manager Internal Controls (Cambridge, MA) You have the opportunity to drive the assessment of risks and internal control over financial reporting (ICoFR). Key activities include performing ICoFR risk impact assessment on new or existing processes, developing and maintaining Corporate SOX framework, advising on the design, implementation of controls,...