Sonja Cuce

Sonja Cuce Email and Phone Number

Regulatory Affairs Consultant, Pharmaceuticals and Medical Device Specialist @ Belsyme Pty Ltd
melbourne, victoria, australia
Sonja Cuce's Location
Greater Melbourne Area, Australia
Sonja Cuce's Contact Details

Sonja Cuce personal email

n/a
About Sonja Cuce

Sonja Cuce is a Regulatory Affairs Consultant, Pharmaceuticals and Medical Device Specialist at Belsyme Pty Ltd. She possess expertise in regulatory affairs, pharmaceutical industry, regulatory submissions, regulatory requirements, gmp and 11 more skills.

Sonja Cuce's Current Company Details
Belsyme Pty Ltd

Belsyme Pty Ltd

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Regulatory Affairs Consultant, Pharmaceuticals and Medical Device Specialist
melbourne, victoria, australia
Website:
belsyme.com.au
Employees:
1
Sonja Cuce Work Experience Details
  • Belsyme Pty Ltd
    Principal Regulatory Affairs Consultant
    Belsyme Pty Ltd Jul 2013 - Present
    Melbourne, Victoria, Australia
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  • Hospira
    Regulatory Affairs Manager
    Hospira 2009 - 2013
    View
  • Hospira
    Senior Regulatory Affairs Associate
    Hospira Mar 2005 - Dec 2008
    View
  • Mayne Pharma
    Regulatory Affairs Associate - Contract Manufacturing
    Mayne Pharma Mar 2004 - Mar 2005
    View
  • Csl Biotherapies Ltd
    Regulatory Affairs Associate
    Csl Biotherapies Ltd Nov 2000 - Mar 2004

Sonja Cuce Skills

Regulatory Affairs Pharmaceutical Industry Regulatory Submissions Regulatory Requirements Gmp Medical Devices Pharmaceutics Capa Biotechnology Change Control Biopharmaceuticals Ectd Oncology Fda Sop Gxp

Frequently Asked Questions about Sonja Cuce

What company does Sonja Cuce work for?

Sonja Cuce works for Belsyme Pty Ltd

What is Sonja Cuce's role at the current company?

Sonja Cuce's current role is Regulatory Affairs Consultant, Pharmaceuticals and Medical Device Specialist.

What is Sonja Cuce's email address?

Sonja Cuce's email address is so****@****.com.au

What skills is Sonja Cuce known for?

Sonja Cuce has skills like Regulatory Affairs, Pharmaceutical Industry, Regulatory Submissions, Regulatory Requirements, Gmp, Medical Devices, Pharmaceutics, Capa, Biotechnology, Change Control, Biopharmaceuticals, Ectd.

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