Auftragsdetails

Freelance Quality Assurance Operations Consultant - Immediate start - propharma group

Datum der Veröffentlichung: Nov 11, 2022
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Auftragsdetails

  • Ort:
    Turin, Torino, Italy
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    5
  • Erfahrung:
    2 Year
  • Geschlecht:
    Keine Präferenz
  • Grad:
    Bachelors
  • 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

Currently we are searching for an independent freelance QA Operations Consultant who will support our client based out of Turin. In this role, the successful candidate will support the QMS revision for audit readiness due to an upcoming audit inspection. The project will be for approximately 160 hours which will equate to 40 hours per week (1.0 FTE) for one month with the ideal start date being as soon as possible.

Essential responsibilities include:

  • Work closely with the Senior Consultant to support the QMS revision
  • Support Quality Assurance aspects in numerous areas to ensure audit readiness
  • Compile and write Quality documentation as and when needed
  • Identify any barriers to ensure audit readiness and implement key changes as and when needed
  • Support other key internal stakeholders when needed
  • Perform routine QA tasks as and when needed
  • Overall support to the client to ensure the successful completion of the project

Qualifications

  • Educated to at least a BSc level or more within a life-science or related discipline (engineering backgrounds would also work with sufficient experience)
  • Substantial experience in the Biological/Pharmaceutical industry is a must
  • Demonstrated experience working in Quality Assurance within the life science industry
  • Exposure in ATMP/Cell therapy would be a distinct advantage
  • Ideally experience gained in gaining audit readiness previously
  • Fluent in Italian and English (a must)
  • Can work office based in Turin (ideally already based in Northern Italy)
  • Immediately availability

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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