Profil #257087

Experienced RA/QA Specialist/Compliance Specialist within QA, Vigilance, Regulatory requirement and audits
Dedicated. Strong quality mind set. Responsible and credible. Adaptability.  
Opdateret 15. marts 2021
Min uddannelse
2003 - 2008

Anden mellemlang videregående udd.

Copenhagen Business School - CBS

Kommunikation inden for jura og medicin
Uddannelsesområde: Medicinal & Sundhed
Periode: oktober 2003 - december 2008
9
1987 - 1988

Ernærings og husholdningsøko.

Suhrs Seminarium, København

Biokemi, biologi (mikro og maktro), kemi.
Uddannelsesområde: Fødevarer & Veterinær
Periode: september 1987 - juli 1988
Min erhvervserfaring
2016 - 2018

RA/QA Specialist

Agilent Technologies

Successful:
product investigation meeting outputs
compliant reporting inkl incidents and FSCAs/Recalls and contact to competent authorities
Support of ongoing internal and cross functional projects
Business wise product decisions balancing regulatory compliance
Regulatory compliance to maintain robust QMS
Arbejdsområde: Medicinal & Sundhed
Periode: august 2016 - september 2018
2007 - 2016

Compliance specialist

LEO Pharma A/S

Managing regulatory surveillance processes and audit programs
Close cooperation with RA/QA implementation of processes and registration of
new products
Support and QC the compliance-monitoring group, to flag emerging issues and
verification of non-compliance
Registrations, applications, reports for the authorities
Arbejdsområde: Medicinal & Sundhed
Periode: juni 2007 - juli 2016
Mine kompetencer
Evner
adaptability coordinator dedicated good communication skills project management responsible and credible strong quality mind set
Sprog på arbejdsniveau
fluency in both verbal and written danish fluency in both verbal and written english
Mine præferencer
Jobtype
Deltidsjob
Arbejdsområde
Medicinal & Sundhed
Geografi
Storkøbenhavn
Læs mere / links
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