Quality Administrator- Remote, Uk - London, United Kingdom - ProPharma Group

ProPharma Group
ProPharma Group
Verified Company
London, United Kingdom

3 weeks ago

Tom O´Connor

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Tom O´Connor

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Description

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.

As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.


ProPharma are looking for a Quality Administrator to join our central team in the UK to support the delivery of Medical Information and pharmacovigilance services, to assurance ongoing quality and industry regulatory requirements.

The Quality Administrator performs improvement activities through continuous monitoring and evaluation of the quality system to ensure ongoing maintenance.


Duties include:

  • Generate and prepare reports to communicate the outcomes of quality activities
  • Analyze and investigate deviation and quality events to identify areas for improvement in the quality system
  • Review, approve and communicate root cause and corrective action to stakeholders
  • Ensures data integrity and accuracy
  • Prepares reports on the results of quality inspections
  • Evaluates outcomes of quality inspections and proposes corrective measure
  • Support the Quality Manager during external client reports
  • Perform effectiveness checks on deviations and quality events to determine efficiency of CAPA's

Requirements:


  • 2+ years experience working within quality within a life sciences setting.
  • Quality systems experience
  • Deviation and CAPA handling experience
  • University and/or Bachelors degree in field related topic
  • 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.

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