Associate Director Quality Assurance

πŸ‡΅πŸ‡± Poland - Remote
πŸ” QAπŸ”΄ Director

Job description

Company Description

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

Come and join us in this exciting journey to make a positive impact in patient’s lives.

Job Description

The Associate Director of Quality Assurance ensures continuous quality improvement through effective management and oversight of audits and inspections. Identifies and implements IT solutions and process efficiencies. Facilitates ongoing quality improvement measures through communication of audit & Inspection intelligence, analytics reports and compliance guidance/training.

The Associate Director of Quality Assurance drives ongoing quality improvement initiatives by disseminating audit and inspection intelligence, delivering comprehensive analytics reports, and providing expert compliance guidance and training.

The Associate Director of Quality Assurance leads the audit and inspection hosting team.

As a leader, the Associate Director of Quality Assurance cultivates a high-performing team, fostering their development into subject matter experts through education, mentorship, and empowerment.

Role and Responsibilities

  • Works with the Director of Quality Assurance to drive excellence and optimizeΒ  audit and Inspection hosting.
  • Participate in audits and inspections, including document request provision, front and back-room activities, and follow-up of audit and inspection findings and completion of client questionnaires and RFP/RFI when needed.
  • Drives ongoing quality improvement measures through communication of audit results and compliance guidance/training.
  • Identifies and implements process improvements and efficiencies via IT solutions.
  • Works with the Quality Assurance Manager to develop and train the hosting team in all activities associated with hosting.
  • Works with the Quality Assurance Manager to continually develop and maintain training material for audit & Inspection attendees.
  • Monitors and communicates trends seen in audits and Inspections to the Director of Quality Assurance.
  • Works with the hosting team to develop and maintains an Inspection knowledge library.
  • Proactively prepares the company and clients for regulatory inspections and audits
  • Collaborates and guides operational personnel to ensure effective audit and Inspection attendance.
  • Generates metrics on audits and Inspections for Global Quality Council, Quality Leadership, Senior Leadership, and Management review purposes.
  • Manages the electronic quality management system (EG-QMS) Audits module. Identifying process improvements and initiating these changes with the relevant IT SME to EG-QMS
  • Fosters a culture of quality within the organisation as led by members of the Quality Leadership Team.
  • Acts as a Subject Matter Expert and client point-of-contact for Quality including attendance at operational and quality governance meetings.
  • Assists in the development, maintenance and management of mechanisms that assure ongoing monitoring and compliance with all applicable laws and regulations including but not limited to EU GVP, US FDA CFRs, JMPA and ICH-E6.
  • Manages the audit and inspection hosting team
  • Conducts other ad hoc activities as requested by Director of Quality Assurance and/or VP of Quality.

Qualifications

  • A university degree in a healthcare discipline or equivalent scientific area
  • Substantial experience in pharmaceutical/biotechnology pharmacovigilance with an in depth understanding of GVP/GCP-related Quality Management and Assurance
  • Sound knowledge of international regulations related to Pharmacovigilance and Medical Information
  • Significant experience of participating in audits and inspections
  • Excellent communication and facilitation skills within a global organization
  • Proactive and self-motivated

SPECIAL SKILLS

  • Strong organizational and planning abilities
  • Excellent problem-solving and decision-making skills
  • Ability to lead, mentor, and develop teams
  • Strong communication and interpersonal skills
  • Attention to detail and commitment to high standards
  • Ability to analyze data and prepare detailed reports
  • Knowledge of quality management principles and practices

Additional Information

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer:

  • Training and career development opportunities internally

  • Strong emphasis on personal and professional growth

  • Friendly, supportive working environment

  • Opportunity to work with colleagues based all over the world, with English as the company language

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships

We look forward to welcoming your application.

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ERGOMED

Clinical research & pharmacovigilance

  • 1001-5000 employees
  • Founded in 1997
  • 16 jobs

Project: Career Search

Rev. 2026.2

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