Current jobs related to CSV Engineer - Boston - Trinity Consultants

  • Senior CSV Engineer

    1 month ago

    Boston, United States LS Solutions Full time

    Position: Senior CSV EngineerDuration: Full Time Location: Remote JOB DESCRIPTIONSenior CSV Engineer Responsibilities:Our team needs a senior level CSV Engineer with ALM experience, ideally with Polarion. Experience with ALM tools such as Kneat, Valgenesis may be considered in lieu of Polarion experience. This person should have strong lab informatics (LIMS,...

  • Senior CSV Engineer

    1 month ago

    Boston, United States LS Solutions Full time

    Position: Senior CSV EngineerDuration: Full Time Location: Remote JOB DESCRIPTIONSenior CSV Engineer Responsibilities:Our team needs a senior level CSV Engineer with ALM experience, ideally with Polarion. Experience with ALM tools such as Kneat, Valgenesis may be considered in lieu of Polarion experience. This person should have strong lab informatics (LIMS,...

  • Senior CSV Engineer

    4 weeks ago

    Boston, United States LS Solutions Full time

    Position: Senior CSV EngineerDuration: Full Time Location: Remote JOB DESCRIPTIONSenior CSV Engineer Responsibilities:Our team needs a senior level CSV Engineer with ALM experience, ideally with Polarion. Experience with ALM tools such as Kneat, Valgenesis may be considered in lieu of Polarion experience. This person should have strong lab informatics (LIMS,...

  • CSV Engineer

    2 months ago

    Boston, United States Trinity Consultants - Advent Engineering Full time

    CSV EngineerLocation: Boston, MAADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and...

  • CSV Engineer

    3 months ago

    Boston, United States Trinity Consultants - Advent Engineering Full time

    CSV EngineerLocation: Boston, MAADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and...

  • CSV Engineer

    1 month ago

    boston, United States Trinity Consultants - Advent Engineering Full time

    CSV EngineerLocation: Boston, MAADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and...

  • CSV Engineer

    6 days ago

    Boston, United States Katalyst Healthcares & Life Sciences Full time

    Responsibilities: Proficient with Computerized systems on Enterprise Level, Lab Systems, and Manufacturing Systems and provide Quality oversight on the related system projects. Take Quality ownership, participate in cross functional team discussions, provide quality guidance/decisions for the projects that includes New implementation,...

  • Validation Specialist

    1 month ago

    Boston, Massachusetts, United States Vastek, Inc. Full time

    Job DescriptionAt Vastek Inc, we are seeking a highly skilled Validation Engineer to join our team. As a key member of our validation program, you will be responsible for ensuring the effective implementation and maintenance of our validation processes. Your expertise will be instrumental in supporting the Validation Manager and tracking/reporting action...

  • CQV Engineer

    1 month ago

    Boston, Massachusetts, United States DPS Group LLC Full time

    Job Title: CQV EngineerWe are seeking a highly skilled CQV Engineer to join our team at DPS Group LLC. As a CQV Engineer, you will play a key role in ensuring the reliability, efficiency, and compliance of our manufacturing processes by leading the qualification efforts for isolator systems used in filling operations.Key Responsibilities:Lead the...

  • Staff Software Engineer, File Ingestion Platform

    1 month ago

    boston, United States 1upHealth, Inc. Full time

    1upHealth is powering the digital transformation of the healthcare industry with our industry-leading platform. By making healthcare data easily accessible and computable, we are on a mission to improve the patient experience, improve the quality of care, and reduce the cost of care.We're looking for an experienced Software Engineer to join the engineering...

  • Staff Software Engineer, File Ingestion Platform

    1 month ago

    Boston, United States 1upHealth, Inc. Full time

    1upHealth is powering the digital transformation of the healthcare industry with our industry-leading platform. By making healthcare data easily accessible and computable, we are on a mission to improve the patient experience, improve the quality of care, and reduce the cost of care.We're looking for an experienced Software Engineer to join the engineering...

  • Staff Software Engineer, File Ingestion Platform

    1 month ago

    Boston, United States 1upHealth, Inc. Full time

    1upHealth is powering the digital transformation of the healthcare industry with our industry-leading platform. By making healthcare data easily accessible and computable, we are on a mission to improve the patient experience, improve the quality of care, and reduce the cost of care.We're looking for an experienced Software Engineer to join the engineering...

  • CQV Engineer

    1 month ago

    Boston, Massachusetts, United States DPS Group LLC Full time

    Job Title: CQV EngineerWe are seeking a highly skilled CQV Engineer to join our team at DPS Group LLC. As a CQV Engineer, you will play a key role in ensuring the reliability, efficiency, and compliance of our manufacturing processes by leading the qualification efforts for isolator systems used in filling operations.Key Responsibilities:Lead the...

  • Senior Data Engineer

    2 months ago

    Boston, United States Arcadis Full time

    Role: Senior Data Engineer (Maximo)  Location: United Kingdom (Remote, with office access) Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets. We are more than 36, people, in over 70 countries, dedicated to improving quality of life. Everyone has an important...

  • Lead Snowflake Developer

    4 weeks ago

    Boston, United States Kforce Technology Staffing Full time

    RESPONSIBILITIES:Kforce has a client in need of a Lead Snowflake Developer in Boston, MA.Responsibilities:* Lead Snowflake Developer will create SQL Procedures in Snowflake* Build Data Pipeline efficiently in a cost-optimizing & performance efficient way* Perform Data loading and unloading of different formats such as CSV, JSON, VARIANT* Create database...

  • Senior Product Analyst

    5 days ago

    Boston, Massachusetts, United States Jobs for Humanity Full time

    About the Role:At FIS, we're committed to advancing the world of fintech. As a Senior Product Analyst - Capital Markets, you'll play a key role in delivering and maintaining leading-edge products and services. Your primary focus will be on promoting the product and vision as defined by the Capital Market Strategy & Product Management teams.Key...

  • IT Project Manager

    1 week ago

    Boston, Massachusetts, United States United Software Group Full time

    Job Description:Seeking an experienced IT Project Manager to oversee the alignment of IT projects with broader business objectives while ensuring regulatory compliance and fostering innovation.This role involves managing the entire project lifecycle, from planning to execution, stakeholder management, risk mitigation, and vendor coordination.Required skills...

CSV Engineer

2 months ago

Boston, United States Trinity Consultants Full time

CSV Engineer Location: Boston, MA ADVENT Engineering is an engineering and consulting firm providing expertise to the pharmaceutical and biotechnology industries. Head-quartered near San Francisco, California, and with operations in the Eastern and Western US, Canada and Singapore, our company is involved in almost every facet of global pharmaceutical and biotechnology facility design and process engineering and quality system projects. ADVENT's services include process engineering, automation engineering, project engineering, facility/system design, start up and commissioning, validation and compliance consulting for distinguished and successful biotechnology and pharmaceutical manufacturing companies. The successful candidate will work with a group of engineers involved in the design, automation, commissioning and start-up of various processes, systems and facilities. A combination of strong technical aptitude, automation engineering skills and technical writing are the desired skill set. This is an outstanding opportunity to join our growing team Responsibilities: Draft and implement Quality System documentation designed to establish good validation practices within the organization. Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards. Design validation approaches, supported by appropriate statistical analyses, perform and/or coordinate all validation activities, analyze and assemble results, and draft validation reports. Perform Data Integrity Assessments and review systems against 21 CFR Part 11 Provide input on user and/or functional requirements of current and future processing equipment, and draft appropriate documentation. Additionally, interface with Manufacturers to ensure all relevant user and functional requirements are met. Provide support to non-engineering Staff, including those from R&D and Manufacturing, to ensure successful technology transfer and continuous improvement. Execute assigned duties on time and pro-actively telegraph delays and other issues to validation manager and other relevant stakeholders. Review DeltaV software and specifications to design test protocols. Comply with all regulatory, corporate, and Quality System policies Qualifications: B.S. / M.S. in engineering or another relevant discipline. Minimum of 4+ years of experience working within an FDA regulated environment. Experience with upstream and downstream equipment is highly desirable. 2+ years’ experience utilizing DeltaV. Capable of interacting with software and designing protocols for DeltaV software customizations. Experience in the areas of Design Documentation (URS, FRS, DS, and other engineering specifications), Validation (IQ, OQ, PQ, PV, CSV, MVP, etc.), Quality Systems (Change Control, Non-Conformances, Requalification, etc) Strong knowledge of Computer Systems Validation lifecycle and documentation. Proficient in Microsoft Word, Excel, PowerPoint. Must be able to work independently with adequate supervision, multi-task, and support several projects simultaneously. Must demonstrate strong communication, interpersonal and teamwork skills. A strong understanding of technical writing and presentation skills is required. **Please note, we are not able to work with any 3rd party vendors or C2C.**