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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our ...

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📑 Recovery Specialist - Women's Residence - WomanPlace (Part Time) Cambridge, MA, USA Req #2483 Tuesday, March 19, 2024 Bay Cove Human Services' mission is to partner with people to overcome challenges and realize personal potential. Bay Cove pursues this mission by providin ...

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📑 Duties: As a key member of commercial operations team, this role will play an integral part in goal of changing patients lives and cultivating our community. You will be responsible for implementing consumer-driven contact tactics across all touchpoints in both a consumer and patient s journey with . The primary focus of this role will ...

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📑 Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Assurance Change Specialist based onsite in our Tewksbury, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans acade ...

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📑 Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components based onsite in our Tewksbury, MA location. CIL is the global leading company in ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 Title: Vendor Quality SpecialistLocation: Fully RemoteContract: 6 months with possibility of conversion Support the GLP/GMP vendor management program, including maintaining the Approved Supplier List, performing vendor risk assessments, audit planning, scheduling, pre-audit meeting schedul ...

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📑 Tellus Solutions is in partnership with a committed biopharmaceutical company in North Chicago focused on providing innovative therapies. Your technical expertise as a QA Specialist I in the Quality Assurance will contribute to our client's innovative therapies which will impact the quality and duration of life.Job ...

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📑 Responsibilities: Interface with customers in various forms of communications including regional forums and specific customer touchpoints, as requested by various teams in the field. Provide data and analysis for customer specific meetings. Proactive Failure Mode Trending to identify emerging issues ac ...

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📑 Summary This position is in Region 1, Laboratory and Applied Science Division, Quality Assurance Branch. About Region 1: This is an office-centered position*--you must physically report to the duty station stated in this announcement on a regular basis. *Work-from-home flexibilities may be authorized as ...

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📑 Description:Working very independently with little guidance from Project Manager and/or Principal Investigator, coordinates all activities of research area including but not limited to supervising the daily activities of research assistants, implementing and maintaining quality assurance procedures, performing statistical analyses, and designing ...

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📑 Vice President, Quality AssuranceShare to LinkedIn Apply Now Apply NowCompany Summary:Leap Therapeutics (Nasdaq: LPTX) is focused on developing targeted and immuno-oncology therapeutics. Leap's most advanced clinical candidate, DKN-01, is a humanized monoclonal antibody targeting the Dickkopf-1 (DKK1) protein. DKN-01 is being developed in patients ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 Responsibilities: Interface with customers in various forms of communications including regional forums and specific customer touchpoints, as requested by various teams in the field. Provide data and analysis for customer specific meetings. Proactive Failure Mode Trending to identify emerging issue ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 Responsibilities: Play a pivotal role in leading statistical programming activities for multiple clinical trials, ensuring the timely and accurate delivery of analysis datasets, tables, listings, and figures. Collaborate closely with cross-functional teams and clients to support the successful exec ...

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📑 Our Purpose and Team:The strategic vision of Sanofi’s Global Medical Device organization is to lead the industry in device-mediated therapies with the ambition to develop, industrialize and maintain best-in-class drug-delivery systems and connected medical devices that are user-centric, innovative, environmentally sustainable, and enhance the value ...

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📑 Title: Compliance Specialist - Level 2Location:- Cambridge, MADuration - 12 months, but we are looking to make it full-time if the contractor performs wellHybrid RemotePay Rate Range:- $61.42 on w2Candidate MUST have a MFG background< ...

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📑 JOB SUMMARYseeking a Contractor Field QA Specialist for the QA Operations organization at the Single Use Facility (SUF) in Devens, MA. The Contractor Field QA Specialist is responsible for quality activities for the Single Use Facility in accordance with policies, standards, procedures, and Global cGMP. Functional responsibiliti ...

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📑 JOB SUMMARY: The purpose of the Quality Assurance Analyst is to provide continuous test improvement and feedback to resolve issues, helping the Automated Fare Collection department meet customer and stakeholder demands by delivering properly performing products in a timely manner. The responsibility of the Quality ...

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📑 JOB SUMMARY:The purpose of the Quality Assurance Analyst is to provide continuous test improvement and feedback to resolve issues, helping the Automated Fare Collection department meet customer and stakeholder demands by delivering properly performing products in a timely manner. The responsibility of the Quality Assurance Analy ...

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📑 Title: Manufacturing Quality AssuranceLocation: Woburn, MADuration: 12+ MonthsClient is a profitable technology company headquartered in Woburn, Massachusetts, USA. Client has developed a proprietary and patented Adaptive Focused AcousticsTM (AFA) technology platform which is utilized in s ...

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📑 Job Description : The purpose of the Quality Assurance Analyst is to provide continuous test improvement and feedback to resolve issues, helping the Automated Fare Collection department meet customer and stakeholder demands by delivering properly performing products in a timely manner. The responsibility of the Quality Assurance ...

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📑 Job Title: Mailroom AssociateJob Location: Lynnfield, MA Pay Rate: $19/hr W2Job Duration: 6 Months Please provide the interview time and day at the top of your resume M-F 2-3 pm ESTSchedule – 4 AM to 12:30 PM (flexible with earlier shifts such as 3 A ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We ...

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📑 Job DescriptionSenior Manager, Quality provides Quality oversight for Bicycle’s development programs, ensuring compliance with applicable ICH GCP and GLP standards and global regulations. As an integral member of the team tasked with product development, the position serves as a Quality and compliance business partner, engaging with multipl ...

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📑 Bicycle Therapeutics (NASDAQ: BCYC) is a clinical-stage biopharmaceutical company developing a novel class of medicines. Our pipeline includes Bicycle Toxin Conjugates® as well as fully synthetic Bicycle® systemic immune cell agonists and Bicycle tumor-targeted immune cell agonists (Bicycle TICAs) focused on oncology indications with high unmet med ...

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📑 Bicycle Therapeutics (NASDAQ: BCYC) is a clinical-stage biopharmaceutical company developing a novel class of medicines. Our pipeline includes Bicycle Toxin Conjugates® as well as fully synthetic Bicycle® systemic immune cell agonists and Bicycle tumor-targeted immune cell agonists (Bicycle TICAs) focused on oncology indications with high unmet ...

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📑 Description: GENERAL SUMMARY/ OVERVIEW STATEMENT: The research assistant (RA) will work on recruitment and testing of subjects for several studi ...

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📑 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 ...

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📑 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 Qu ...

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📑 Responsibilities: Regulatory Compliance & Quality Systems Specialist / Sr. Specialist looking for 2-3 staff in this area, also with 10+ years of experience supporting oper ations regulatory inspections, audits, and working within the Quality Systems of Change Control, Nonconformances and Correctiv ...

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📑 Position Details: Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for a Quality Assurance Specialist to join their expanding team.Job Title: Quality Assurance Specialist / Pharma Drug Substance Testing / Hybrid work Duration: 12 months contract, ...

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📑 Position Details: Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for a Quality Assurance Specialist to join their expanding team.Job Title: Quality Assurance Specialist / Pharma Drug Substance Testing / Hybrid work Duration: 12 months contract, ...

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📑 Responsibilities Develops and executes manual and automated test plans and test suites for new and existing products as required. Plans, creates, maintains, and executes detailed test plans, and test cases for verification of, but not limited to, software functionality, security, load, and performance. ...

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📑 Primary Talent Partners has a full-time, 13-month contract Principal Quality Engineer opening with a Fortune 500 Medical Device client located in Billerica, MA. Pay range for this position is $60 to $70 per hour based on overall experience. Overview:We are seeking a highly skilled and experienced Pr ...

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📑 On-Board Services is hiring a Scientific - Laboratory Specialistin Cambridge, MA! For immediate consideration please send your resume to Subject Line: Position Title and State you are Located. About Us:On-Board Services, ...

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📑 The Specialist will develop, update, and maintain IT compliance documentation based on IT compliance standards. The individual will conduct regular reviews and assessments to coordinate System (Client) Enterprise Risk Management and Security Assurance for the (SAFR) reporting requirements. Responsibilities - Perform IT compliance, risk assessmen ...

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📑 At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our ...

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📑 Security System Specialist-(3279676) Description Summarize the nature and level of work performed. The Security Systems Specialist plays a pivotal role in ensuring the safety and security of patients, visitors, and employees within Public Safety Operations by overseeing the coordination, integration, i ...

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📑 The position directly supports Vedanta’s in-house cGMP manufacturing capabilities including programs in multiple phases of development. This role will be focused on supporting environmental monitoring and quality data review, with the opportunity to be involved in other aspects of quality control work.Perform routine Environmental Monitoring (EM) a ...

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📑 The position directly supports Vedanta’s in-house cGMP manufacturing capabilities including programs in multiple phases of development. This role will be focused on supporting environmental monitoring and quality data review, with the opportunity to be involved in other aspects of quality control work.Per ...

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📑 Job duties: Develop and execute software tests to identify software problems and their causes. Create test plans, scripts, and test data. Perform product testing, UAT, remote testing, and performance testing. Prepare UAT and functional test cases. Conduct system analysis, and identify and resolve problems. Test design improvements through the devel ...

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📑 Job title: Senior Quality Assurance Analyst Job duties: Develop and execute software tests to identify software problems and their causes and ensure completion of test planning and execution activities associated with all aspects of technology project life cycle. Conduct User Acceptance Testing and Post depl ...

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📑 Title: Quality Engineer, Design AssuranceLocation: Woburn, MADuration: 12+ MonthsJob Summary: We are seeking a skilled Design Assurance Engineer or Systems Engineer to join our team as a contractor for a 9-12 month term. Reporting to the Director of QA/RA, the Q ...

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📑 Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Assurance Associate I based onsite in our Tewksbury, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, p ...

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📑 QA Tester Location: Northampton Bill rate: /hr shift: Rotating days (M, T, Fri, Sat) next week (Wed, Thurs, Sun) times: 5:45am-6:15pm Function Specific Activities The following is a list of top Function-Specific activities performed in the job. <br ...

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📑 If you are interested in this job and need more details, please send me (Harpreet) your resume on (url removed) and call/ text me on (phone number removed). Thanks!Job Title: QA TesterLocation: Northampton, MA, 01060Duration: 04 Months ContractHo ...

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📑 QA TesterLocation: Northampton, MA3 Months contractPay Rate: $20/hr on w2shift: Rotating days (M, T, Fri, Sat) next week (Wed, Thurs, Sun)times: 5:45am-6:15pmFunction Specific ActivitiesThe following is a list ...

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