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Regulatory Specialist II
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Collabera Santa Clara, United StatesHome · Search Jobs · Job Description · Regulatory Specialist II · Contract: Santa Clara, California, US · Salary: $45.00 Per Hour · Job Code: · End Date: · Days Left: 11 days, 3 hours left · Apply · To discuss more about this job opportunity, please reach out to Chitrank ...
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Regulatory Specialist II
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Collabera Santa Clara, United StatesHome · Search Jobs · Job Description · Regulatory Specialist II · Contract: Santa Clara, California, US · Salary: $45.00 Per Hour · Job Code: · End Date: · Days Left: 3 hours left · Apply · To discuss more about this job opportunity, please reach out to Chitrank Rastogi ...
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Regulatory Specialist II
1 week ago
Collabera Santa Clara, United StatesHome · Search Jobs · Job Description · Regulatory Specialist II · Contract: Santa Clara, California, US · Salary: $45.00 Per Hour · Job Code: · End Date: · Days Left: 8 days, 3 hours left · Apply · To discuss more about this job opportunity, please reach out to Chitrank ...
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Regulatory Specialist II
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Collabera Santa Clara, United StatesHome · Search Jobs · Job Description · Regulatory Specialist II · Contract: Santa Clara, California, US · Salary: $45.00 Per Hour · Job Code: · End Date: · Days Left: 1 days, 3 hours left · Apply · To discuss more about this job opportunity, please reach out to Chitrank ...
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Regulatory Specialist II
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The Fountain Group Santa Clara, United StatesHello, · This is ShivaRaj from · The Fountain Group, · we are currently seeking a · Regulatory Specialist II · for a prominent client of ours. This position is located in · Santa Clara, CA. · Details for the position are as follows: · Pay: $60-56 · Experience: · 2-5 yea ...
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Regulatory Affairs Specialist
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GForce Life Sciences Santa Clara, United StatesRegulatory 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 man ...
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Regulatory Specialist II #:
2 weeks ago
HireTalent group Santa Clara, United States1 week ago Be among the first 25 applicantsExempt/Non Exempt: Non Exempt Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge of regu ...
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Regulatory Specialist II #:
3 weeks ago
HireTalent group Santa Clara, United States1 week ago · Be among the first 25 applicants · Exempt/Non Exempt: Non Exempt Years Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or scientific affairs function Skills: Knowledge o ...
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Regulatory Affairs Specialist
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GForce Life Sciences Santa Clara, United StatesRegulatory 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 comme ...
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Regulatory Affairs Specialist
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GForce Life Sciences Santa Clara, United StatesRegulatory 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 comm ...
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Regulatory Specialist II
5 days ago
Collabera Santa Clara, United StatesHome · Search Jobs · Job Description · Regulatory Specialist II · Contract: Santa Clara, California, US · Salary: $45.00 Per Hour · Job Code: · End Date: · Days Left: 5 days, 3 hours left · Apply · To discuss more about this job opportunity, please reach out to Chitrank ...
Regulatory Specialist II - Santa Clara, United States - Collabera
Description
Job Description
Job 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 supporting internal and external inspections.
· Work cross-functionally and in a matrixed environment Have experience with continuous improvement activities.
· Education: BA Degree Required. Bachelor's degree in Science, Math, Engineering or Medical Fields preferred.
· Duties: This position will be providing support for the regulatory department to ensure efficient and compliant business processes and environment.
· The individual may execute tasks and play a consultative role by partnering across business functions and suppliers.
· The individual may assist in identifying data needed, obtaining these data and ensuring that they are effectively presented for the registration of products worldwide.
· The individual may prepare and submit documentation needed for registration worldwide or may oversee such preparation.
Company DescriptionCollabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data/AI. With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.
