Regulatory Specialist
2 weeks ago
Title:- Regulatory Specialist II
Duration:- 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 systems
Company DescriptionSelect Source International (SSI) is an IT, Health Care, and Engineering Services consulting firm that has been in business since 1998. SSI consultants have provided exceptional services that have been appreciated by clients, customers, and users alike at several large Fortune 500 companies, mid-size enterprises, and consulting companies.Company DescriptionSelect Source International (SSI) is an IT, Health Care, and Engineering Services consulting firm that has been in business since 1998. SSI consultants have provided exceptional services that have been appreciated by clients, customers, and users alike at several large Fortune 500 companies, mid-size enterprises, and consulting companies.-
Regulatory Affairs Specialist
4 weeks ago
Santa Clara, United States GForce Life Sciences Full timeRegulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2Job 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 Specialist
3 weeks ago
Santa Clara, United States GForce Life Sciences Full timeRegulatory 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 Specialist
4 weeks ago
Santa Clara, United States GForce Life Sciences Full timeRegulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2Job 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 Specialist II
24 hours ago
Santa Clara, United States DivIHN Integration Full timeDivIHN (pronounced "divine") is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to...
-
Regulatory Affairs Specialist
4 weeks ago
Santa Clara, United States GForce Life Sciences Full timeRegulatory 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 Specialist
1 week ago
Santa Clara, United States Select Source International Full timeJob Description Job Description Title:- Regulatory Specialist II Duration:- 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 systems Company...
-
Regulatory Specialist
2 days ago
Santa Monica, United States alphapro technology, a.p.r., inc. Full timeOverview: **Duties**: - Develop and implement regulatory strategies for product approvals and compliance - Ensure adherence to FDA regulations and guidelines - Coordinate and support regulatory submissions for new products or changes to existing products - Conduct regulatory research and stay current on industry regulations - Collaborate with...
-
Regulatory Specialist II
3 weeks ago
Santa Clara, United States Collabera Full timeJob 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...
-
Regulatory Affairs Specialist
1 week ago
Santa Clara, United States LanceSoft Full timeJob Title: Regulatory Operations Location: Santa Clara, CA 95054 Duration: 6 Months Description / 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...
-
Regulatory Specialist
4 days ago
Santa Fe Springs, United States Astrix Full timeOur client is a successful chemical manufacturer who offers contract manufacturing, and the development of cleaning and sanitizing products to prevent illnesses and provide for safe, clean food for families across the nation!The Regulatory Compliance Specialist assures, together with relevant functions, early and effective regulatory compliance assessments...
-
Regulatory Specialist
2 days ago
Santa Fe Springs, United States Astrix Inc Full timeOur client is a successful chemical manufacturer who offers contract manufacturing, and the development of cleaning and sanitizing products to prevent illnesses and provide for safe, clean food for families across the nation! The Regulatory Compliance Specialist assures, together with relevant functions, early and effective regulatory compliance assessments...
-
Child Life Specialist
2 days ago
Santa Clara, United States Kaiser Permanente Full time**Job Summary**: Meets the psychosocial needs of hospitalized children through a play activity program. Provides play opportunities and other experiences in order to minimized the negative emotional and developmental impact of hospitalization, within the CSA. **Essential Responsibilities**: - Provides appropriate play activities for the ambulatory and...
-
Santa Clara, United States Kaiser Permanente Full timeJob Summary: Meets the psychosocial needs of hospitalized children through a play activity program. Provides play opportunities and other experiences in order to minimized the negative emotional and developmental impact of hospitalization, within the CSA. This position is primarily based in the outpatient subspecialty department, although the specialist may...
-
Specialist
2 weeks ago
Santa Clara, United States HCL Technologies Ltd. Full timeJob Description (Posting). Replacement PRF (1.) To provide support for on call escalations and doing root cause analysis of given issue (2.) To independently resolve tickets within agreed SLA of ticket volume and time (3.) To adhere to quality standards, regulatory requirements and company policies (4.) Work on value adding activities such Knowledge base...
-
Senior Specialist
2 weeks ago
Santa Clara, United States HCL Technologies Ltd. Full timeJob Description (Posting). refer jd (1.) To provide support for on call escalations and doing root cause analysis of given issue (2.) To independently resolve tickets within agreed SLA of ticket volume and time (3.) To adhere to quality standards, regulatory requirements and company policies (4.) Work on value adding activities such Knowledge base update...
-
Medical Device Quality Engineer I
4 days ago
Santa Clara, United States Anatomage Full timeWho is Osteoid?Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry. Proven in over ten years of use by thousands of labs and dental practices, Osteoid's software and hardware tools keep dental practices and labs ahead of the curve and allow dentists to...
-
Medical Device Quality Engineer I
2 weeks ago
Santa Clara, United States Anatomage, Inc. Full timeJob DescriptionJob DescriptionWho is Osteoid?Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry. Proven in over ten years of use by thousands of labs and dental practices, Osteoid’s software and hardware tools keep dental practices and labs ahead of...
-
Medical Device Quality Engineer I
5 days ago
Santa Clara, United States Osteoid Inc Full timeJob DescriptionJob DescriptionSalary: $75,000 to $78,000About the RoleWe are looking for a Quality Engineer or Specialist to join our rapidly expanding team. As a member of our Quality & Regulatory team, you’ll be responsible for developing and maintaining our quality system for our medical device products. Together as a team, you’ll help ensure our...
-
Hazardous Materials Specialist, Senior
1 week ago
Santa Barbara, United States Santa Barbara County, CA Full timeCoordinates and conducts the more difficult, complex regulatory oversight of facilities that are permitted as hazardous waste generators, underground storage tanks, and hazardous materials establishments involving a multitude of industrial processes, Materials, Specialist, Public Health, Senior, Chemistry, Environmental, Healthcare
-
Medical Device Quality Engineer I
3 weeks ago
Santa Clara, California, United States Anatomage, Inc. Full timeWho is Osteoid? Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry. Proven in over ten years of use by thousands of labs and dental practices, Osteoid’s software and hardware tools keep dental practices and labs ahead of the curve and allow dentists...