Manager, Quality Assurance, Central EPM

Reposted 8 Days Ago
Be an Early Applicant
Hiring Remotely in Warszawa, Mazowieckie
In-Office or Remote
Senior level
Pharmaceutical • Manufacturing
The Role
As the QA Manager, you'll ensure compliance with regulatory standards, lead quality initiatives, conduct audits, and support continuous improvement in healthcare operations.
Summary Generated by Built In

Medison offers hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets.

As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live.

Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve.

We are a dynamic, fast-paced company, operating in over 34 countries across 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us!

We’re hiring QA Manager in Poland!

As Quality Assurance Manager, you’ll play a pivotal role in ensuring our operations meet the highest regulatory standards and deliver exceptional quality across your market. In this position, you will lead compliance efforts, drive continuous improvement, and support processes that make a real impact on patients and partners.

Required Education and Experience:

  • Master’s or Bachelor’s degree in Science or equivalent
  • Minimum 5 years of experience in an active QA role within the healthcare or pharmaceutical sector
  • Strong knowledge of regulatory requirements, including GDP and GMP
  • Proven track record in auditing and quality systems, including experience as a quality auditor; experience in regulatory inspections is desirable
  • Ability to act as a quality function representative on various projects
  • Expertise in root cause analysis, investigations, and technical report writing
  • Experience in SOP creation and updates, as well as other quality documentation
  • Excellent written and verbal communication skills; fluent English is essential
  • Strong critical thinking, problem-solving, and decision-making skills
  • High attention to detail and strong organizational abilities
  • Collaborative, self-directed, and able to work independently.

Required Qualifications:

  • Excellent interpersonal skills with the ability to build and maintain professional, trusting relationships
  • Strong ability to work effectively in highly dynamic and changing environments; demonstrates agility and adaptability
  • Willingness to travel locally and internationally as needed
  • Flexible personality with the ability to collaborate horizontally and vertically across the organization; capable of influencing, managing conflict, and driving solutions
  • Quick learner with strong work ethic and pragmatic approach focused on results
  • High attention to detail and strong organizational abilities
  • Ability to identify and understand issues, problems, and opportunities while providing viable solutions
  • Able to work in a fast-paced, dynamic environment and adjust readily to meet unexpected constraints.

Top Skills

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Gmp
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The Company
Petach Tikva
627 Employees
Year Founded: 1996

What We Do

Medison is a global pharma company focused on providing access to highly innovative therapies to patients in international markets.

Medison is the first to create an international commercialization platform for highly innovative therapies, helping to save and improve lives by making the best available novel treatments accessible to patients in international markets.

Medison has a track record of global partnerships with leading pharmaceutical and biotech companies seeking to expand their global reach.

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