Auftragsdetails

Senior Consultant Quality Assurance /QP/RP (REF11101V) - propharma group

Datum der Veröffentlichung: Nov 11, 2022
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Auftragsdetails

  • Ort:
    Leiden, South Holland, Netherlands
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    5
  • Erfahrung:
    3 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Masters
  • Vorher bewerben:
    Nov 30, 2023

Job Summary

Company Description

ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

Detailed Description

Job Description

Within our Division Life Science Consulting we are recruiting experienced Quality Assurance, Qualified Persons (QP and/or RP) who are ready to enter the world of consultancy. It is expected that you are able and willing to dig into the details yet keeping an eye on the overall goal of the project. This person is result- and clients oriented and have adequate interpersonal skills. Must feel comfortable working with deadlines in an often changing environment and see it as a challenge to solve issues in a pragmatic and proactive way.

Qualifications

Qualified candidates must have:

  • 5 years or more in GMP related areas as Qualified Person and Responsible Person 
  • Experience in development (R&D) and commercial as QP or RP
  • Experienced in working with MS Word and Excel
  • Enthusiastic & self-starter
  • Exposure to working with Biological products preferred 
  • Excellent knowledge of requirements for GMP and GDP
  • Good understanding of GMP and GDP, regulatory requirements in EU as well as US and RoW
  • Excellent in both English and Dutch language, both written and verbal
  • Proficiency or fluency in another language is a benefit

Additional Information

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

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Company Overview

Berlin, Berlin, Germany

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving the pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio... Read More

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