Associate Quality Manager (f/m/d)

Reposted 2 Days Ago
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Vienna, AUT
In-Office
3K-3K Annually
Mid level
Healthtech • Pharmaceutical
The Role
The Associate Quality Manager will oversee quality assurance activities, manage compliance, lead audits, and develop the Quality Management System in line with pharmaceutical regulations.
Summary Generated by Built In

Associate Quality Manager - FTC

Location: Vienna, Austria (Hybrid)

Department: Quality Assurance

Job type: 12-month Fixed-Term Contract

Join us and make a difference when it matters most! 

At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. 

The Team

We are looking for an Associate Quality Manager to join Mundipharma on a 12‑month fixed‑term contract. In this role, you will support and maintain a robust pharmaceutical Quality Management System in line with the Austrian Medicines Act (AMBO) and EU GDP / GxP guidelines, covering Austria and selected CEE markets. You will work closely with cross‑functional and regional stakeholders and play a hands‑on role in day‑to‑day quality operations. This is an excellent opportunity to deepen your experience in GDP/GMP‑related Quality Assurance within an international pharmaceutical environment.

Role and Responsibilities

  • Regional QA Oversight - Plan and monitor Quality Assurance activities across Austria and the CEE markets to ensure operational compliance.

  • Issue Resolution and support the management of regional quality issues, including complaints, product recalls, and returns.

  • Audit Management - Lead the preparation and support for internal and external GDP/GMP audits and regulatory inspections.

  • QMS Development - Maintain and evolve the Quality Management System in accordance with EU GDP/GMP guidelines and national legislation.

  • Quality Controls - Manage deviations, CAPAs, change controls, and conduct thorough quality risk assessments.

  • Oversee technical documentation Quality/Technical Agreements, pharmaceutical licenses, and ensure rigorous document control.

  • Develop and maintain core documentation, including SOPs, the Quality Manual, and the Site Master File (SMF).

  • Monitor quality KPIs and contribute to monthly reviews and Product Quality Reviews (PQRs).

  • Compliance Monitoring - Conduct self-inspections and manage NMVO alerts and related regional contracts.

  • Act as a proactive interface for stakeholders, providing expert quality guidance and training compliance support to regional teams.

What you’ll bring

  • University degree in Pharmacy would be ideal but may be open to other Scientific Degrees in areas such as Chemistry, Biology, Human or Veterinary Medicine, Dentistry, or Food/Biotechnology

  • Previous experience in pharmaceutical quality assurance

  • Solid understanding of GDP/GMP and pharmaceutical quality systems

  • Previous experience in use of QMS (Trackwise would be ideal but open to others)

  • Analytical, solution‑oriented, and detail‑focused working style

  • Hands‑on mentality with a strong sense of ownership and self‑motivation

  • Strong communication skills and ability to collaborate across functions and regions

  • Open mindset, pragmatic approach, and strong team orientation

  • Customer‑ and patient‑focused way of working

  • Fluent German and English (German at native level)

What we offer in return

  • Opportunity to work in a regulated pharmaceutical environment with regional exposure.

  • Hands‑on Quality role with real responsibility and impact.

  • Supportive team and structured handover due to maternity leave cover.

  • Fixed‑term role ideal for building or strengthening Quality Assurance expertise.

For this position, the minimum salary according to the collective agreement for full-time employment is €2,986.00 gross per month. However, we offer a market-competitive overpayment depending on qualifications and experience. 

Diversity and inclusion

Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority. We believe this isn’t just the right thing, but also the smart thing to do. We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness. We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect. 

About Mundipharma

Mundipharma is a global healthcare company focussing on customers across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.  

Mundipharma is dedicated to bringing innovative treatments to patients in the areas of pain management, infectious disease as well as other severe and debilitating disease areas. Their guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything they do. For more information visit www.mundipharma.com.  

Join our talent pool

If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles.


Additional Job Description:

Primary Location:

AT Vienna

Job Posting Date:

2026-04-22

Job Type:

Fixed Term Contract (Fixed Term)

Skills Required

  • University degree in Pharmacy or related scientific field
  • Previous experience in pharmaceutical quality assurance
  • Solid understanding of GDP/GMP and pharmaceutical quality systems
  • Experience using QMS (preferably Trackwise)
  • Fluent in German and English

Mundipharma Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Mundipharma and has not been reviewed or approved by Mundipharma.

  • Flexible Benefits A choice-based scheme lets people flex life insurance and income protection above core levels, indicating a tailored approach. Documented updates to benefits design show active management of options to suit individual needs.
  • Healthcare Strength Private medical coverage and critical illness options are included within a flexible package in at least one major hub. Health-focused measures and protections are highlighted alongside core benefits.
  • Leave & Time Off Breadth Paid sick leave, a solid annual holiday allowance with public holidays, and volunteering leave are described. Time-off approvals are positioned as supportive where operational cover allows.

Mundipharma Insights

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The Company
Cambridgeshire
2,154 Employees
Year Founded: 1952

What We Do

Mundipharma is a global healthcare company with a presence across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. Mundipharma is dedicated to bringing innovative treatments to patients in the areas of Pain Management, Infectious Disease and Consumer Healthcare as well as other severe and debilitating disease areas. Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. We encourage our people to think differently and our inclusive culture of continuous learning and collaboration make Mundipharma a great place to work. For more information visit www.mundipharma.com See our community guidelines: mundipharma.com/social-media-community-guidelines

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