Auftragsdetails

Quality Consultant - Permanent opportunity - (REF10671R) - propharma group

Datum der Veröffentlichung: Nov 12, 2022
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Auftragsdetails

  • Ort:
    Stockholm, Stockholm, Sweden
  • Gesellschaft:
  • Typ:
    Full Time/Permanent
  • Shift:
    First Shift (Day)
  • Karrierelevel:
    Experienced Professional
  • Positionen:
    4
  • Erfahrung:
    3 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

ProPharma are continuing to expand our market leading services in Quality Assurance across the EU and we are now looking to add to our team in Sweden with our newest ‘Quality Consultant’. In this pivotal function, you will get the chance to work on some of the most fascinating and challenging projects within the Life science sector both on a strategic and operational level. You will also get the chance to expand your skill set into different therapeutic areas and work on variety of tasks both within the Pharmaceutical and Biological industry.  

Essential responsibilities will include:

  • Provide strategic advice, project management, auditing, CAPAs/deviations, support tech transfers, qualification/validation support, Quality documentation management etc.
  • Evaluate current quality methods for a variety of clients and offer both strategic and operational support in identifying areas which could be improved
  • Oversee and maintain the Quality Management System for assigned clients, as applicable.
  • Conduct audits and participate in regulatory inspections for clients in collaboration with the authorities.
  • Provide internal and external training/education
  • Utilise your understanding of regulatory guidelines to offer key support to help our clients facilitate improvements to their quality management system 
  • Participate in a wide range of projects from development to commercialised products

Qualifications

  • Must be educated to at least a BSc within a life science discipline or a related field
  • Ideally we are looking for at least 3-6 years exposure working within Quality Assurance within the Pharmaceutical or Biological industry
  • Fluent skills in English and Swedish/Danish are a must
  • Strategic and operational skills would be preferred
  • Excellent communication skills
  • Ability to build key relationships across a variety of stakeholders
  • Driven, hungry to learn and adaptable

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.***

Fähigkeiten benötigt

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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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