Global Medical Affairs Lead

The position requires that they develop an understanding of the Clip products and manufacturing processes in order to review and assess proposed product changes within the change management system (in Change Orders and Change Requests). **Specific responsibilities will include**: - RA Lead / Core Team Support for manufacturing related submissions - RA Lead...

The person in this role may work remotely within the US or onsite at a US-based Medtronic facility. CAREERS THAT CHANGE LIVES The strategic intent of the newly designed Global Operations and Supply Chain (GO&SC) Operating Unit is to create a more agile and responsive manufacturing and supply chain organization. One that anticipates and meets the needs of our...

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...

Education: Bachelor's degree required, Master’s degree preferred Experience: Minimum of 3 years of Regulatory Affairs experience Skills Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or device submissions. Hands-on experience with 510k submission, or PMA/s or US Annual...

Regulatory Affairs Project Lead– Santa Clara, CAMust 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...

Title: Regulatory Affairs Project Leader Location: Santa Clara, California Duration: 12 Months Education: Bachelor's degree required Masters degree preferred Experience: Minimum of 3 years experience Skills: Knowledge of US and/or Canadian regulation relating to product and/or device clearance (FDA) Duties: Assists in definition/implementation of regulatory...

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– 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– 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...

Job DescriptionJob Description·         Education: Bachelor's degree required, Master’s degree preferred·         Experience: Minimum of 3 years of Regulatory Affairs experience·         Skills: Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or...

Job DescriptionJob Description·         Education: Bachelor's degree required, Master’s degree preferred·         Experience: Minimum of 3 years of Regulatory Affairs experience·         Skills: Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or...

Title:Regulatory Affairs Project LeaderLocation:Santa Clara, CaliforniaDuration: 12 MonthsEducation:Bachelor's degree requiredMasters degree preferredExperience:Minimum of 3 years experienceSkills:Knowledge of US and/or Canadian regulation relating to product and/or device clearance (FDA)Duties:Assists in definition/implementation of regulatory strategy and...

Job Description Job Description Education: Bachelor's degree required, Master's degree preferred Experience: Minimum of 3 years of Regulatory Affairs experience Skills: Knowledge of US and/or Canadian regulations or with EU and other international medical device regulations relating to product and/or device submissions.· Hands-on experience with 510k...

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...

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...

Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary Were 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...

Regulatory 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...