Regulatory Windchill Coordinator

Job DescriptionJob DescriptionSMS Staffing Inc is Hiring Immediately for a skilled Regulatory Windchill Coordinator. Job Title: Regulatory Windchill CoordinatorJob Location: Sylmar, CA, U.S.A.Job Type: Contract (possible conversion)Pay: Starts at $40.00 an hourShift Structure: 8:00 am - 5:00 pm PST; ONSITE, Monday to Friday, 40 hours per weekAbout the...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill CoordinatorLocation: 91342, Los Angeles, California, United StatesDuration: 06 MonthJob Description:This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person...

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. ...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as well...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as well...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as well...

Company Description Valiance Clinical Research is an interdisciplinary research center located in Los Angeles, California. We are focused on changing the future of healthcare through clinical trials. Our facility is equipped to perform clinical trials from Phase 1 studies to Phase 4. We prioritize ease of startup, efficient recruitment and retention, as...

General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Remote Fully On-Site Work Schedule Monday - Friday 8am - 5pm (hours may vary) Posted Date 01/29/2024 Salary Range: $28.78 - 59.34 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 12279 Primary Duties and...

General Information Press space or enter keys to toggle section visibility Work Location: Los Angeles, USA Onsite or Remote Fully On-Site Work Schedule Monday - Friday 8am - 5pm (hours may vary) Posted Date 01/29/2024 Salary Range: $28.78 - 59.34 Hourly Employment Type 2 - Staff: Career Duration Indefinite Job # 12279 Primary Duties and...

Description Under the direction of the Operational Managers, Investigators, Financial Administrative Office, Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU) the Regulatory Coordinator is responsible for preparation, submission and maintenance of regulatory applications to fulfill...

DescriptionUnder the direction of the Operational Managers, Investigators, Financial Administrative Office, Faculty, Medical and Administrative Directors of the Jonsson Comprehensive Cancer Center (JCCC) Clinical Research Unit (CRU) the Regulatory Coordinator is responsible for preparation, submission and maintenance of regulatory applications to fulfill...

Job Description Job Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

The UCLA CORE Kidney Health Program is seeking an experienced RegulatoryProject Manager to oversee all regulatory aspects of clinical trials, clinical programs,our patient and community outreach program, education and training, and assistwith administrative tasks. You will be responsible for the oversight ofregulatory coordination for clinical research...

Client: IRIDEX Position: Regulatory Affairs Associate Location: Mountain View, CA Contract Length: 5 months Pay Range: $35 - $45/hr IRIDEX Corporation is a medical device manufacturer and operates in a global regulated environment (e.g. FDA). Regulations include (but are not limited to) FDA 21 CFR 820, EN ISO 13485, Health Canada SOR/ 98-282, and the...

Job DescriptionJob Description PureTek is a dynamic and innovative company specializing in developing and manufacturing pharmaceutical and cosmetic products. With a commitment to quality, safety, and regulatory compliance, we strive to deliver products that enhance the well-being and beauty of our consumers. Join our team and contribute to our mission of...

Position Summary The primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for our client's product...

Grow your career at Cedars-Sinai! The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and trainin Regulatory, Clinic, Research, Clinical Research, Coordinator, Healthcare