Manufacturing Electronic Test Engineer
Acuity
ERP
Compliance and Quality Assurance Consultant
ProPharma
full-time
Posted on:
Location Type: Office
Location: 🇭🇷 Croatia
Visit company websiteJob Level
JuniorMid-Level
About the role
- Provide operational support to QA activities linked to the complaint process for one global life-sciences client
- Support returns processing, temperature excursion evaluation, alert handling and related tasks
- Support and lead deviation management as and when directed
- Support other QMS tasks for clients based within the EU
- Work towards expanding skills and aim at becoming a Responsible Person or Qualified Person
- Initially support a single product complaint management project on a 1-year fixed term contract, with likely transition to permanent role
Requirements
- Must be educated to at least a BSc level or higher within a life-sciences discipline
- At least 2-4 years’ experience already gained with Quality Assurance for a Pharmaceutical or Biological group (a must requirement)
- Previous experience with complaint management linked to QA activities (GMP, GDP) would be highly preferred
- Fluency in English
- Can commence a new project immediately full time for one year or more
- Excellent communication skills
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Quality Assurancecomplaint managementdeviation managementGMPGDP
Soft skills
communication skills
Certifications
BSc in life-sciences
