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Senior Quality Assurance Analyst Job
Eingestellt von Yoh
Gesuchte Skills: Engineering, Client
Projektbeschreibung
THE BIG PICTURE - TOP SKILLS YOU SHOULD POSSESS:
- 3 - 5+ years of experience in regulatory affairs
- Working knowledge of US and international regulations and guidance including but not limited to FDA 21 CFR, CMDCAS ISO 13485, IVDD
- Experience in biomedical industry
WHAT YOU'LL BE DOING:
- Responsible for executing the post-market regulatory strategy and deliverables for all company's product lines.
- Prepare and submit recall/field action reports to worldwide regulatory agencies or authorities in various impacted geographies
- Compile necessary information.
- Establish and maintain metrics using Excel or various reporting tools
- Perform other related duties and assignments as required
WHAT YOU NEED TO BRING TO THE TABLE:
- Master's degree in Science (Chemistry, Biochemistry, Biology) or Regulatory Affairs with 3 years of experience or Bachelor's degree in Science (Chemistry, Biochemistry, Biology) or Engineering (Chemical or Biomedical) with 5 years of relevant experience
- Working knowledge of US and international regulations and guidance including but not limited to FDA 21 CFR, CMDCAS ISO 13485, IVDD
- Experience in biomedical industry
WHAT'S IN IT FOR YOU?
- This is your chance to work for a company that cares about your development and helps lead you to where you want to be
RECRUITER:Jillian Valdez
Yoh, a DayJ2W: SCIENTIFIC; MONJOB
TAX FORM: CON_W2 J2WBRSTL
Ref:
SFSF: LS
Projektdetails
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Einsatzort:
Brea, Vereinigte Staaten
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik