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Minimum of 5 years of experience as a Developer/Business Systems Analyst with a focus on QMS in the medical device industry, including expertise in Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
$80 - $85ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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QualificationsBachelor’s degree or higher in environmental management, environmental science, physical science, or related fieldMinimum of five years field experience that should include:Project managementClient relationsSite samplingEmergency/spill responseSite characterization and remediationCoordination with permitting and regulatory authoritiesCPESC/CESSWI CertificationDOT/RCRA CertificationCHMM, Hazwoper a plusMust have strong oral and written communication skills.
$130,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with the TMF Reference Model, GCP and GDP standards and applicable Regulatory requirements. Our successes have enabled our team to experience the full range of drug development—from the development of our in-house scientific platform, which has enabled pioneering insights into new biological mechanisms, to the discovery and development of first-in-class therapies that exploit those mechanisms, through to regulatory approval.
$70,030 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We seek outstanding candidates with teaching experience in the following: industry experience in entrepreneurship, drug/ medical device development, data science, regulatory affairs, clinical and medical affairs, quality management, project management, finance, business operations, research and development, biometrics, health economics and outcomes research or manufacturing.
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Work collaboratively with Manufacturing, QA and Regulatory to support CMC analytical deliverables. Author and revise SOPs, deviations, CRs and LIRs. Areas of responsibility include but are not limited to testing samples for Appearance, pH, UV and water content, HPLC, ELISA, western blot and SDS-PAGE as needed.
$30 - $37 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Recommend solutions for required changes to life support systems based on analyses of water quality data, system trends, animal observations, regulatory and water discharge requirements, and water flow needs, in collaboration with Applied Water Science, Husbandry, and other departments.
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This Senior Regulatory Affairs Specialist position is an on-site opportunity working out of our Santa Clara, CA location in the Abbott Vascular Division. As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.
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Basic understanding of regulatory affairs concepts, guidelines, and regulations governing the development, documentation, and labeling of in vitro diagnostic products. Kelly® Science & Clinical is currently recruiting for a Technical Writer for a 6-month contract opportunity with a leading molecular diagnostics company at their headquarters in Sunnyvale, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology realm.
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FCS is looking for On-Call Biological Field Monitors / Technicians (CG03) who will participate in construction monitoring sites throughout California to support federal, state, and local regulatory requirements.
$35 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Summary: The Compliance Manager will help design, implement, and monitor the Company's various compliance initiatives, including the Company's export control compliance program and procedures, code of business conduct, whistleblower hotline, internal investigation activities and communications, ESG and sustainability initiatives, and training in FCPA/anti-corruption, antitrust/anti-monopoly/anti-unfair competition, and other legal and regulatory areas.
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Must meet basic requirements of local child care regulatory agency (Title 22) including immunization, health screening,finger-printing and background checkMust be able to lift up 35 lbs. Keywords: preschool, teacher, infant, toddler, childcare, care, daycare, children, caregiver, preschools, child, children, kids, summer camp, after school, extended day, substitute, transitional kindergarten, jr.
$22 - $28 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversee grants and contracts to ensure timely completion of promised deliverables and communication with funders; design and adapt service delivery methods to meet regulatory, contractual obligations and client needs.
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They are also the STEWARDS of the company, delivering accurate financial reports, prudent financial risk management, compliance to external regulatory requirements (requires an understanding of local accounting, tax legislation and regulations) and performing proofing in local and US GAAP financial Statements including reconciliation vs IFRs/ US GAAP/Tax. They are also business process specialists, championing SIMPLIFICATION while delivering the business objectives.
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Knowledge of regulatory requirements and safety standards associated with the design, build, and automation of electro-mechanical and opto-mechanical systems, with experience supporting laser-based systems is highly desired.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Experience focused on quality systems, regulatory affairs/compliance or project management. ASQ Certified Quality Engineer (CQE), Auditor (CQA) and/or Six Sigma Green Belt a plus. Overview: Responsible for supporting development and implementation of Quality Management System (QMS) and supporting infrastructure/tools in compliance with FDA Quality System Regulation (QSR) regulations, International Standards Organization (ISO) regulations, and corporate requirements.
$38 - $43ExpandApply NowActive JobUpdated Today
regulatory job Title: regulatory affairs specialist Company: Parexel in Milpitas, CA
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