Auftragsdetails

Freelance - Computer System Validation Manager - 12 month project - propharma group

Datum der Veröffentlichung: Nov 11, 2022
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Auftragsdetails

  • Ort:
    Berlin, Berlin, Germany
  • Gesellschaft:
  • Typ:
    Freelance
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    3
  • 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 looking for an independent contractor/freelancer to work on an exciting and long term project for one of our clients based within the Pharmaceutical industry. In this function, the successful applicant will need to be well versed in CSV and have exposure to working on Manufacturing execution systems. The project would require the individual to be available for 12 months and be able to offer full-time services (1.0FTE) throughout the whole period.

Essential Functions Include:

Working on Manufacturing execution systems which includes tasks such as:

  • Devising a Validation strategy  
  • Creating a Validation (Master) Plan
  • Producing Specifications
  • Create design qualifications
  • Ensure Configuration on the specifications are created and correct
  • Conducting Risk Assessments & Risk Analysis
  • Conducting Test cases
  • Provide key training to a range of stakeholders

Qualifications

  • B.S./B.A. in Engineering, Science, Information Technology or related field..
  • Extensive experience in the field of Computer System Validation within a life science setting
  • Must have demonstrated experience working on Manufacturing execution systems
  • Fluent in English and ideally advanced skills in reading German documents
  • Can work remotely but attend site visits in central Germany when required
  • Can commit to a 12 month project at full time hours (1.0FTE)

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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