Mirva Boothe Email & Phone Number
@prevas.se
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Who is Mirva Boothe? Overview
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Mirva Boothe is listed as Senior Consultant Life Science Medical Devices based in Sweden, Sweden, Sweden. AeroLeads shows a work email signal at prevas.se and a matched LinkedIn profile for Mirva Boothe.
Mirva Boothe previously worked as Senior Consultant Life Science Medical Devices at Prevas Ab and Senior Quality & Regulatory Consultant at Medqure Consultancy. Mirva Boothe holds Master Of Science, Chemical Engineering from Kth Royal Institute Of Technology.
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AeroLeads found 1 current-domain work email signal for Mirva Boothe. Compare company email patterns before reaching out.
About Mirva Boothe
Mirva Boothe is a Senior Consultant Life Science Medical Devices at -. They possess expertise in lifesciences, fda, validation, biotechnology, regulatory submissions and 8 more skills.
Listed skills include Lifesciences, Fda, Validation, Biotechnology, and 9 others.
Mirva Boothe's current company
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Mirva Boothe work experience
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Senior Consultant Life Science Medical Devices
Senior Quality & Regulatory Consultant
Team Lead Intertek Medical Notified Body
- The Clinical Team Lead has accountability to ensure Intertek Medical Notified Body has clinical oversight of medical device conformity assessments in line with the requirements in:
- EU Medical Device Directives 93/42/EEC and applicable guidance documents
- REGULATION (EU) 2017/745 of the European Parliament and of the Council on medical devices Technical Documentation Assessor - Review technical documentation.
Regulatory Affairs, Md Nordics
Ensure regulatory compliance of Medical Devices for their access to the Nordic market. Establish and maintain processes and procedures linked to Regulatory Affairs activities. Be the primary internal and external contact point within the region for operational regulatory affairs needs. Local J&J representative in Swedish MedTech Regulatory Affairs sector.
Regulatory Affairs Manager
Experienced QA/RA manager. QA/RA in development projects, PMS and audits. Liable for regulatory submissions to multiple countries including EU, USA and Canada. Responsible for oversight and internal training of the European MD directive and regulation. Expert role within the department for biocompatibility and sterilization. Member of standard committee.
Regulatory Affairs Manager
Temporary position to help with quality assurance and regulatory workload. Update the processes for CE marking and active role in audits.Responsible for Technical Files/Design Dossier updates for the European region and premarket submissions to USA. QA representative of assigned development projects, involved in risk management, usability and clinical.
Research Scientist
Research Associate / Research Scientist
Senior Analytical Chemist / Senior Research Scientist
Mirva Boothe education
Master Of Science, Chemical Engineering
University Certificate In Medical Laboratory Technology, Clinical Chemistry
Frequently asked questions about Mirva Boothe
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What is Mirva Boothe's role at their current company?
Mirva Boothe is listed as Senior Consultant Life Science Medical Devices.
What is Mirva Boothe's email address?
AeroLeads has found 1 work email signal at @prevas.se for Mirva Boothe.
Where is Mirva Boothe based?
Mirva Boothe is based in Sweden, Sweden, Sweden.
What companies has Mirva Boothe worked for?
Mirva Boothe has worked for Prevas Ab, Medqure Consultancy, Intertek Sweden, Johnson & Johnson, and Maquet Critical Care Ab / Getinge Group.
How can I contact Mirva Boothe?
You can use AeroLeads to view verified contact signals for Mirva Boothe, including work email, phone, and LinkedIn data when available.
What schools did Mirva Boothe attend?
Mirva Boothe holds Master Of Science, Chemical Engineering from Kth Royal Institute Of Technology.
What skills is Mirva Boothe known for?
Mirva Boothe is listed with skills including Lifesciences, Fda, Validation, Biotechnology, Regulatory Submissions, Regulatory Affairs, Gmp, and Drug Development.
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