Regulatory Affairs Specialist

Regulatory Affairs Specialist Santa Clara, CA Must be able to work on a W2 Job Summary: We are seeking a regulatory affairs specialist to assist and lead in the definition/implementation of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry. Key Responsibilities:...

Regulatory Affairs Specialist– Santa Clara, CA Must be able to work on a W2 Job Summary: We are seeking a regulatory affairs specialist to assist and lead in the definition/implementation of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry.Key...

Regulatory Affairs Specialist– Santa Clara, CA Must be able to work on a W2 Job Summary: We are seeking a regulatory affairs specialist to assist and lead in the definition/implementation of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry.Key...

Regulatory Affairs Specialist II Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry. Your responsibilities include maintaining the quality system, supporting manufacturing operations, and providing regulatory guidance. Experience with international...

Regulatory Affairs Project Lead Santa Clara, CA Must be able to work on a W2 Job Summary: We are seeking a regulatory affairs specialist to assist and lead in the definition/implementation of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry. Key Responsibilities:...

Regulatory Affairs Associate – Santa Clara, CA MUST BE ABLE TO WORK ON A W2Job Summary:The Regulatory Affairs Compliance Support role is pivotal in ensuring adherence to regulatory standards by providing crucial support to the Regulatory Affairs (RA) organization. The position involves driving key performance indicator (KPI) dashboards, managing strategic...

Regulatory Affairs Associate – Santa Clara, CA MUST BE ABLE TO WORK ON A W2Job Summary:The Regulatory Affairs Compliance Support role is pivotal in ensuring adherence to regulatory standards by providing crucial support to the Regulatory Affairs (RA) organization. The position involves driving key performance indicator (KPI) dashboards, managing strategic...

Job Title: Regulatory OperationsLocation: Santa Clara, CA – 95054Duration: 6 MonthsDescription / Summary:This role will provide compliance support to the Regulatory Affairs organization by –a. Driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metrics.b. Managing strategic program for RA audit...

Job Title: Regulatory OperationsLocation: Santa Clara, CA – 95054Duration: 6 MonthsDescription / Summary:This role will provide compliance support to the Regulatory Affairs organization by –a. Driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metrics.b. Managing strategic program for RA audit...

Job Title: Regulatory OperationsLocation: Santa Clara, CA – 95054Duration: 6 MonthsDescription / Summary:This role will provide compliance support to the Regulatory Affairs organization by –a. Driving preparation of KPI dashboards and maintaining a pulse on formal RA management review and internal metrics.b. Managing strategic program for RA audit...

The Fountain Group is a national staffing firm and we are currently seeking a Regulatory Affairs Associate for a prominent client of ours. This position is located in Santa Clara, CA Details for the position are as follows: Job Description: Details: Pay for this position is 40.00 to 45.00 hourly depending on experience. This position is a contract with the...

Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II - Neuromodulation About the role: Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements....

Recruiter: Spencer Gregory Hale Regulatory Affairs Specialist II – Neuromodulation About the role:Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory...

Job DescriptionJob DescriptionPosition OverviewTo be successful in this role, you should have at least ten years of experience in the pharmaceutical industry or a related field. You should also have knowledge of FDA cGMP requirements, ISO standards, ICH guidelines, and quality management systems. You should have excellent communication, grammar, spelling,...

**The McGuff Company Inc. is growing and looking to hire a Regulatory Affairs Manager** McGuff values its employees as one of its most important resources. We strive for a vibrant, healthy work culture and attain it through good communication, active involvement, and corporate responsibility. We leverage our employees’ expertise and support their...

Recruiter: Spencer Gregory HaleRegulatory Affairs Specialist II - NeuromodulationAbout the role:Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements.Your...

Job DescriptionJob Description·         Must have 3-5 years of experiences in Medical Device Regulatory Affairs Skills.·         Have working knowledge in EU MDR.·         Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device submissions.·         Have experience...

Job Description Job DescriptionMust have 3-5 years of experiences in Medical Device Regulatory Affairs Skills.Have working knowledge in EU MDR.Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device submissions.Have experience supporting internal and external inspections.Work cross-functionally and in a...

Job DescriptionJob DescriptionTitle:- Regulatory Specialist IIDuration:- 6+ Month Seeking candidate with experience with international (outside of EU and US) product registrations; experience working with medical device operations on control of product release; experience working with electronic change management/document control systemsCompany...

Job Title: Medical Affairs Information System Specialist (Pharma/Biotech)Work Location: Santa Monica, CAW2 Contract & Onsite role One of our leading Pharmaceutical client is looking for a Medical Affairs Information System Specialist, who will support client Medical Affairs on their digital technology needs. Required Experience:5+ years of experience working...