- Twist BioScience (South San Francisco, CA)
- The Regulatory Operations Specialist is responsible for ensuring the efficient and compliant management of regulatory documentation, with a primary focus on ... global product compliance, ensuring that all documentation accurately reflects regulatory requirements and product specifications.What You'll Be Doing Initiate,… more
- Solina (Bolingbrook, IL)
- …through our customers culinary vision making "Food Matter." SUMMARY OF POSITION The Regulatory Specialist assists in ensuring products meet regulatory ... ingredient statements and nutritional data to meet customer and regulatory requirements. Maintains accurate ingredient information in necessary databases and… more
- Barghausen Consulting Engineers, Inc. (Kent, WA)
- We are looking for a Permitting & Regulatory Compliance Specialist II to join our growing team in Kent, WA. Pay is DOE: $35-$40/hr *The pay range offered to the ... We offer tuition reimbursement to support your learning journey. Permitting & Regulatory Compliance Specialist II Job Responsibilities: Understand fuel design… more
- Envista (Brea, CA)
- Job Description: The Regulatory Affairs Specialist is responsible for assembling CE Technical files and final review of deliverables for MDR regulatory ... Certificate of Foreign Government and Certificates of Free Sale Resolve regulatory issues and ensure companywide compliance. Reviews regulatory publications… more
- Globus Medical (Audubon, PA)
- …can resume their lives as quickly as possible. Position Summary: The Regulatory Affairs Specialist assists with drafting, submitting and gaining clearance ... needed for IDE and PMA reporting Reviews Document Change Orders for Regulatory compliance, including drawings and labeling changes Performs routine maintenance of… more
- Cedent (Boston, MA)
- As a Clinical Trial Regulatory Affairs Specialist , you will be responsible for: * Regulatory Compliance: Ensuring all clinical trials adhere to applicable ... EMA, and ICH standards *Documentation Management: Preparing, reviewing, and submitting regulatory documents, such as Investigational New Drug (IND) applications and… more
- EPM Scientific (Philadelphia, PA)
- …in the ophthalmic medical device industry, is seeking an experienced and driven Regulatory Affairs Specialist to join their team in Pennsylvania. This position ... regulatory strategy and supporting innovative product development. The Regulatory Affairs Specialist should have the following qualifications: Bachelor's… more
- System One Holdings, LLC (Cranbury, NJ)
- Job Title : Food Safety & Regulatory Compliance Specialist Location : Cranbury, NJ Hours / Schedule: Monday - Friday, 8am - 4pm, onsite Type: Direct Hire ... Responsibilities The Food Safety & Regulatory Compliance Specialist is responsible for managing and coordinating food safety and quality systems while ensuring… more
- Boston Scientific (Irvine, CA)
- …Urology solutions. We are looking to hire an enthusiastic individual for a Regulatory Affairs Specialist III position supporting our rapidly growing active ... implantable device portfolio. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product… more
- Cleerly (Denver, CO)
- …be listed as requirements in the job description. About the Opportunity As Principal Regulatory Affairs Specialist , you will provide regulatory support and ... documents. Excellent organizational, writing and verbal communication skills. Principal Regulatory Affairs Specialist (Specific) Experience: Minimum 3 years'… more
- CorDx (San Diego, CA)
- …of the most critical questions in healthcare. Job Type: Full time Job Title: Regulatory & Compliance Specialist Location: Onsite - San Diego Salary Range: ... $90,000 - $95,000 Position Summary: The Quality and Regulatory Compliance Specialist is responsible for ensuring that development processes for all in vitro… more
- Eisai, Inc (Nutley, NJ)
- …cognitive impairment due to Alzheimer's disease (AD) or mild AD. The Neurology Account Specialist (NAS) will be part of a diverse team of sales professionals who ... marketplace.Seek out mentorship to learn and build key sales skills. Qualifications: Specialist - ADBachelor's degree with 3+ years experience in two or more of:… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionTitle: Specialist , Metrology and Validation, Analytical Research & DevelopmentJob Description-The Analytical Research & Development (AR&D) External ... Research Laboratories Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility. The… more
- Eisai, Inc (Raleigh, NC)
- …difference. If this is your profile, we want to hear from you. The QA Specialist plays a critical role in ensuring the quality and compliance of commercial and ... is responsible for executing core quality assurance functions, supporting regulatory inspections, and collaborating with internal and external stakeholders to… more
- Merck & Co. (Omaha, NE)
- …time. -We are seeking a Growth and Improvement minded Associate Specialist , Logistics who can help drive our Strategic Operating Priorities.Strategic SummaryThe ... Associate Logistics Specialist will be responsible for export of raw materials...closely with freight forwarders, QA departments, USDA and other regulatory officers. Provide data to the Finance department so… more
- Merck & Co. (Durham, NC)
- …several years; currently Durham employs 1,000+ people. Durham's Technology Transfer Specialist will be an energetic, technical leader with strong interpersonal, ... process understanding Author, review, and/or edit technical documents to support regulatory filings including technical reports and risk assessments Author or… more
- Aequor (Thousand Oaks, CA)
- …work alongside other innovative, driven professionals in this meaningful role. Role: Specialist Manufacturing, New Product Introduction Let's do this! At we strive ... for the introduction of new products into the manufacturing plant. This " Specialist Manufacturing" role will serve as a New Product Introduction Lead within… more
- Merck & Co. (South San Francisco, CA)
- …enhance document authoring processes, thereby improving efficiency and compliance in regulatory submissions.The candidate will play a key role in developing, ... to streamline the creation and quality control (QC) of regulatory submission documents. The candidate will be part of...GenAI models to automate the compilation and QC of regulatory submission documents and reports -. -Collaborate with principal… more
- Aequor (Hicksville, OH)
- Packager - Support Specialist 2nd shift Packaging = /hr pay rate rd Shift Packaging = /hr pay rateImportant that they are able to work on the 1st shift (6:45 am - ... to all applicable procedures, cGMP's, company policies, and all other quality or regulatory requirements (OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.). Ensures all work… more
- Aequor (Athens, GA)
- Tech-savvy information management specialist to support GI Development sites / activities. Major activities include: the subject matter expert for electronic ... records from legacy systems. Electronic Document Management (controlled documents, regulatory submission documents): Create and configure document templates and… more
