QA Associate (student position)

Posted 2 Days Ago
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Zagreb, Grad Zagreb
1-3 Years Experience
Biotech • Pharmaceutical
The Role
The QA Associate will assist the QA team in managing audits and inspections, support functional teams pre- and post-audit, maintain audit trackers, and contribute to CAPA activities. Responsibilities include document management, scheduling audits, and supporting the Global Quality Function.
Summary Generated by Built In

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 QA Associate will support the QA team to ensure internal/external audits are developed, managed, maintained, and delivered in line with PrimeVigilance procedures.

The QA Associate will conduct all activities described, including but not limited to:

  • Hosts/supports audits (routine, due diligence, qualification) and inspections of Primevigilance performed by clients/third parties and regulatory authorities as agreed with Quality Audits Manager and/or Director, Quality
  • Supports PrimeVigilance functional teams pre-, during and post-audit by clients or by internal QA function
  • Assists in client specific requests for audit scheduling
  • Assists in maintenance of trackers involved for audit related tasks and the maintenance of the SharePoint
  • Supports the oversight, maintenance, scheduling of audits and inspections of PrimeVigilance performed by clients/third parties and regulatory authorities.
  • CAPA Support Activities
  • Supports in tracking of the vendor audit CAPAs.
  • Support in the facilitation and review of vendor CAPA responses
  • Input into the global audit CAPA tracker
  • Ensures documents and trackers from internal system and/or vendor audits initiated by Primevigilance, are kept up to date.
  • Assists in the development and maintenance of the internal risk assessments.
  • The QA Associate will also support the Global Quality Function as needed.
  • Other QA support as needed

Qualifications

  • Previous experience in the pharmaceutical and/or regulated industry in a quality setting – preferably in Pharmaceuticals or Healthcare
  • Good overview of the principles of Quality Assurance
  • Experience of participating in audits and inspections
  • Excellent communication and facilitation skills within a global organization
  • Organization skills, including attention to details and multitasking
  • English advanced – spoken and written

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 Ergomed is a great company to join!

  • Quality 
  • Integrity & Trust
  • Drive & Passion
  • Agility & Responsiveness
  • Belonging 
  • Collaborative Partnerships

We look forward to welcoming your application!

The Company
HQ: Raleigh, NC
535 Employees
On-site Workplace
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.

• 1,400+ highly qualified professionals
• Global full-service CRO
• 25+ years of experience
• Therapeutic specialization in oncology
• Strong expertise in rare disease trials
• Robust clinical safety system
• Choice of leading drug safety databases

Our key services include:
• Clinical Research Services
• Pharmacovigilance
• Medical Information
• Regulatory
• Medical Writing
• Site Management
• Study Physician Support
• Biostatistics
• Patient Study Support

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