Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Sr. Regulatory Affairs Specialist

Glaukos Corporation

Sr. Regulatory Affairs Specialist role at Glaukos Corporation Sr. Regulatory Affairs Specialist (Hybrid - Acton, MA) The Sr. RA Specialist is Responsible for preparation of regulatory submissions (domestic and foreign). Ensure implementation and maintenance of regulatory filing in compliance with applicable regulations and Glaukos internal SOPs. Seniority level Mid-Senior level Employment type Full-time Job function Legal Industries Medical Equipment Manufacturing Location Hybrid - Acton, MA #J-18808-Ljbffr Glaukos Corporation

Vacancy posted 6 days ago
Similar jobs that could be interesting for youBased on the Sr. Regulatory Affairs Specialist in Burlington, MA vacancy
  • The Sr. RA Specialist is Responsible for preparation of regulatory submissions (domestic and foreign). Ensure implementation and maintenance of regulatory filing...  ...regulatory agenciesAssist with other basic Regulatory Affairs functions, such as scanning and archiving records... 
    Senior
    Local area

    Glaukos

    Burlington, MA
    4 days ago
  • Job SummaryThe Sr. Associate, Compliance is responsible for overseeing vendor management and ensuring supplier quality compliance,...  ...effective follow-up.Ensure vendor-supplied products comply with regulatory and quality standards.Develop and maintain strong, long-term relationships... 
    Senior

    Sun Pharmaceutical Industries

    Billerica, MA
    4 days ago
  •  ...Senior Regulatory Affairs Specialist BrioHealth Solutions is seeking a skilled and self-motivated Senior Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular Assist System. This individual will partner with cross-functional teams to support product... 
    Senior

    BrioHealth Solutions, Inc.

    Burlington, MA
    2 days ago
  • BRIOHEALTH SOLUTIONS INC, based in Massachusetts, seeks a Senior Regulatory Affairs Specialist to lead FDA submissions and regulatory planning for BrioVAD LVAS. You will partner with cross-functional teams to ensure compliance across US and EU programs, including IDE/PMAs... 
    Senior

    BRIOHEALTH SOLUTIONS INC

    Burlington, MA
    3 days ago
  • Glaukos Corporation in Acton, MA, is seeking a Sr. Regulatory Affairs Specialist to lead the preparation of regulatory submissions for the U.S. and international markets. The role is hybrid and full-time, requiring a proactive regulatory mindset and collaboration with cross... 
    Senior
    Full time

    Glaukos Corporation

    Burlington, MA
    6 days ago
  • Position Summary The Manufacturing Compliance Specialist serves as the compliance subject matter expert within Manufacturing, ensuring cell therapy operations are executed in accordance with cGMP, regulatory requirements, and internal quality systems. Key Responsibilities... 
    Senior
    Weekend work
    Afternoon shift

    Scorpion Therapeutics

    Burlington, MA
    2 days ago
  • $135k - $155k

     ...Epicel and Nexobrid (burn care). The Manufacturing Compliance Specialist serves as the compliance subject matter expert within...  ...accordance with current Good Manufacturing Practices (cGMP), regulatory requirements, and internal quality systems. This position partners... 
    Senior
    Hourly pay
    For contractors
    Monday to Friday
    Shift work
    Weekend work
    Afternoon shift

    Vericel® Corporation

    Burlington, MA
    2 days ago
  • $94k - $150k

    Job TitleSenior Regulatory Affairs SpecialistJob DescriptionSenior Regulatory Affairs Specialist, UltrasoundThe Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory teams and authorities to secure timely product clearances. Responsibilities... 
    Senior
    Full time
    Work at office
    Immediate start
    Work visa
    Relocation package
    3 days per week

    Philips

    Cambridge, MA
    4 days ago
  • $101.6k - $131.9k

     ...tough problems. Job Summary Responsible for supporting regulatory activities regarding released product, including, MDR investigations...  ...field required. A minimum of 4 years of direct Regulatory Affairs experience is required, including preparation of Pre-IDEs, 510... 
    Senior
    Shift work

    Meridian Bioscience

    North Billerica, MA
    4 days ago
  • Job DescriptionMIT Lincoln Laboratory is a Department of Defense Federally Funded Research and Development Center (FFRDC) engaged in the development and demonstration of advanced prototype technologies and systems, with an overall objective to transfer those capabilities...
    Senior
    Contract work
    Work at office

    Lincoln Laboratory

    Lexington, MA
    3 days ago
  • Sun Pharmaceutical Industries, Inc (USA) seeks a Sr. Associate Compliance to provide scientific support for root cause analysis and closure of OOS and OOT investigations and product quality complaints. You will ensure GLP and cGMP compliance and contribute to the Quality... 
    Senior

    Sun Pharmaceutical Industries, Inc.

    Billerica, MA
    2 days ago
  •  ...Regulatory Affairs Specialist II The Regulatory Affairs Specialist II supports regulatory submissions and regulatory authority interactions related to product submissions and approvals. In this role, you will prepare and submit regulatory documentation, support product... 

    Anika Corporation

    Bedford, MA
    3 days ago
  •  ...markets worldwide.Support product registrations, including creating, revising, reviewing and compiling documents for submission to regulatory authorities, as well as assisting in responding to questions and requests from such authorities.Assist in external audits by... 
    Worldwide

    Cedent Life Talent

    Bedford, MA
    4 days ago
  • $140k - $180k

     ...including third-party risk, control testing, and audit readiness—while ensuring the organization is prepared for certifications and regulatory requirements. Additionally, you will enhance our security posture through automation, continuous monitoring, and proactive... 
    Senior

    NetBrain Technologies

    Burlington, MA
    2 days ago
  • Position Overview This position is intended to provide Regulatory Affairs support to FUJIFILM Healthcare Americas Corporation. This position supports full, ongoing compliance to all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements... 
    Local area
    Remote work
    Flexible hours

    FUJIFILM Holdings America Corporation

    Lexington, MA
    5 days ago
  • Anika-GCC in Bedford, MA is seeking a Regulatory Affairs Specialist II to support regulatory submissions and regulatory authority interactions related to product submissions and approvals. You will prepare and submit regulatory documentation, support product market approval... 

    ANIKA-GCC

    Bedford, MA
    2 days ago
  • Anika is seeking a Regulatory Affairs Specialist II to support regulatory submissions, authority interactions, and post-approval activities. The role requires preparing documentation, maintaining compliance, and guiding cross-functional teams through regulatory processes... 

    Anika Corporation

    Bedford, MA
    3 days ago
  •  ...and disappointment. Every person has their own story. We strive to make your story at AspenTech a great one. Your Impact The Role As a Sr Principal Solution Consultant, you will collaborate closely with AspenTech sales teams to lead consultative discovery sessions, craft... 
    Senior

    Aspen Technology, Inc.

    Bedford, MA
    3 days ago
  • Sr. Java Developer Required: Sr. Java Developer with strong experience on Java, ReactJs, Oracle DB. Experience in Spring Boot. Rest API Services. Requirement gathering, writing reusable code. Identify bugs and resolve them.
    Senior

    Syntricate Technologies

    Burlington, MA
    2 days ago
  • $168k - $218.3k

    Qorvo (Nasdaq: QRVO) supplies innovative semiconductor solutions that make a better world possible. We combine product and technology leadership, systems-level expertise and global manufacturing scale to quickly solve our customers' most complex technical challenges. Qorvo...
    Senior

    Qorvo

    Chelmsford, MA
    5 days ago
  • The individual will be responsible for developing new PWB/PWA/Flex designs and the transition of those designs into military qualified hardware. The individual should be proficient in specifying the appropriate PWB/PWA/Flex construction based on requirements and environments...
    Senior
    Flexible hours

    Judit Inc

    Wilmington, MA
    12 hours ago
  •  ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the... 
    Immediate start

    Artech

    Cambridge, MA
    3 days ago
  • $179k - $236k

     ...and present DMPK and translational biomarker data to internal leadership and external stakeholdersAuthor nonclinical sections of regulatory filings (e.g., IND) and briefing documents; support agency interactions and responsesServe on the Research Leadership Team; represent... 
    Senior

    Seres Therapeutics

    Cambridge, MA
    4 days ago
  • $147.4k

    Posting Description SENIOR LICENSING AND BUSINESS DEVELOPMENT OFFICER, Technology Licensing Office, is responsible for the commercialization of MIT’s IP portfolio arising from research and activities on MIT’s campus; managing a large portfolio of cases, including, technology...
    Senior
    Full time
    Work at office
    Visa sponsorship

    Massachusetts Institute of Technology

    Cambridge, MA
    1 day ago
  • AspenTech is seeking a Sr Principal Solution Consultant to partner with the sales team to lead discovery sessions, craft strategic solutions, and design customer-focused implementation strategies. You will leverage deep industry knowledge for Metals & Mining, Specialty... 
    Senior

    Aspen Technology, Inc.

    Bedford, MA
    3 days ago
  • EMD Serono seeks a Senior Principal Biostatistician to shape the statistical foundation of life‑changing medicines. You will serve as a Statistical Subject Matter Expert at the program level, designing, analyzing, and interpreting data across clinical and observational ...
    Senior

    Biopharma Careers

    Billerica, MA
    2 days ago
  • A leading technology company is seeking a Senior Principal Software Engineer to join their Xcelium Compiler Team. This role focuses on implementing advanced compiler algorithms and collaborating on strategic architectural initiatives for simulation technologies. Candidates...
    Senior

    Cadence Inc

    Burlington, MA
    3 days ago
  •  ...Advisory practice. You will work on a variety of healthcare projects, including compliance program development, data analysis, and regulatory risk assessment, leveraging strong analytics and client-facing skills. The role offers upward career trajectory, collaboration... 
    Senior

    Baker Tilly US

    Tewksbury, MA
    4 days ago
  •  ...Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.As a Senior Clinical Regulatory Specialist at Iterative Health, you will play a key role in supporting the compliant execution of Phase 2-4 industry-sponsored clinical... 
    Senior
    Temporary work
    Work at office
    2 days per week

    Iterative Scopes

    Cambridge, MA
    2 days ago
  •  ...Job Description Insight Global is looking for a Sr. Engineering Technician in the Wilmington MA area. The ideal candidate will have between 15-20 years of experience working in precision assembly in a development environment. This candidate will be highly independent... 
    Senior

    Insight Global

    Wilmington, MA
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Sr. Regulatory Affairs Specialist. Be the first to apply!