Regulatory Affairs Manager

Company description: SynCardia Systems, LLC, a Picard Medical Company, is headquartered in Tucson, AZ. We manufacture and sell the world's first and only US Food and Drug Administration (FDA) and Health Canada approved total artificial heart as bridge to transplant for patients suffering from biventricular heart failure The SynCardia Total Artificial...

Job DescriptionJob DescriptionCompany description:SynCardia Systems, LLC, a Picard Medical Company, is headquartered in Tucson, AZ. We manufacture and sell the world's first and only US Food and Drug Administration (FDA) and Health Canada approved total artificial heart as bridge to transplant for patients suffering from biventricular heart failure The...

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche,...

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche,...

Job Description Regulatory Affairs Manager (European Union expertise) Medical Device Company. Tucson, AZ Onsite (relo over time) 140k Talentry is looking for a Regulatory Affairs expert with medical device experience in the European Union (EM MDR). This expert will aid in the preparation of documentation, submissions, applications, responses, adverse...

Job DescriptionJob DescriptionRegulatory Affairs Manager (European Union expertise)Medical Device Company. Tucson, AZOnsite (relo over time) 140kTalentry is looking for a Regulatory Affairs expert with medical device experience in the European Union (EM MDR). This expert will aid in the preparation of documentation, submissions, applications, responses,...

JOB PURPOSE: Provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual will execute tasks and play a consultative role by partnering across business functions. The individual will assist in identifying data needed, obtaining these data and ensuring that they are effectively presented...

JOB PURPOSE: Provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual will execute tasks and play a consultative role by partnering across business functions. The individual will assist in identifying data needed, obtaining these data and ensuring that they are effectively presented...

JOB PURPOSE: Provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual will execute tasks and play a consultative role by partnering across business functions. The individual will assist in identifying data needed, obtaining these data and ensuring that they are effectively presented...

JOB PURPOSE: Provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual will execute tasks and play a consultative role by partnering across business functions. The individual will assist in identifying data needed, obtaining these data and ensuring that they are effectively presented...

JOB PURPOSE: Provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual will execute tasks and play a consultative role by partnering across business functions. The individual will assist in identifying data needed, obtaining these data and ensuring that they are effectively presented...

Seeking an experienced Regulatory Compliance Supervisor with experience in manufacturing process controls in medical device/plastics environment. You will be responsible for medical device regulatory requirements; 21 CFR Par 11, 21 CFR Part 820, ISO-13485, regulatory submissions to the FDA and other regulatory agencies. Ideal candidate will have a degree in...

**Position Description**: **Salary Grade: 12** **Pay Range** **Hiring Range: $54,863 - $65,836 Annually** **Full Range: $54,863 - $76,809 Annually** Join a dynamic team of environmental professionals monitoring the water quality of surface waters, wells, and water reclamation facilities throughout eastern Pima County. As a water quality coordinator for the...

Seeking Quality Systems Supervisor with experience in manufacturing process controls with experience in injection molding or contract manufacturing. You will be responsible for regulatory requirements; 21 CFR Par 11, 21 CFR Part 820, ISO-13485, regulatory submissions to the FDA and other regulatory agencies. Ideal candidate will have a degree in a discipline...

Seeking Quality Systems Supervisor with experience in manufacturing process controls with experience in injection molding or contract manufacturing. You will be responsible for regulatory requirements; 21 CFR Par 11, 21 CFR Part 820, ISO-13485, regulatory submissions to the FDA and other regulatory agencies. Ideal candidate will have a degree in a discipline...

**Position Description**: **Salary Grade: 10** **Pay Range** **Hiring Range: $23.92 - $28.71 Per Hour** **Full Range: $23.92 - $33.49 Per Hour** **Duties/Responsibilities**: (Work assignments may vary depending on the department's needs and will be communicated to the applicant or incumbent by the supervisor.) Reviews and prepares permit documents and...

Job DescriptionSeeking Quality Systems Supervisor with experience in manufacturing process controls with experience in injection molding or contract manufacturing.  You will be responsible for regulatory requirements; 21 CFR Par 11, 21 CFR Part 820, ISO-13485, regulatory submissions to the FDA and other regulatory agencies.  Ideal candidate will have a...

Seeking Quality Systems Supervisor with experience in manufacturing process controls with experience in injection molding or contract manufacturing. You will be responsible for regulatory requirements; 21 CFR Par 11, 21 CFR Part 820, ISO-13485, regulatory submissions to the FDA and other regulatory agencies. Ideal candidate will have a degree in a discipline...

ABOUT CRITICAL PATH INSTITUTE (C-PATH) Critical Path Institute (C-Path) is a nonprofit engaged in the creation of partnerships and innovative processes that improve human health by reducing the time, cost, and risk in developing and approving new therapies. For over ten years, we have partnered with industry and academic experts to advance technologies...

ABOUT CRITICAL PATH INSTITUTE (C-PATH) Critical Path Institute (C-Path) is a nonprofit engaged in the creation of partnerships and innovative processes that improve human health by reducing the time, cost, and risk in developing and approving new therapies. For over ten years, we have partnered with industry and academic experts to advance technologies...