Quality Specialist - Warsaw, Polska - Novo Nordisk

Opis

The position

In this position, you will play a pivotal role in upholding the integrity and efficiency of our regional office's Quality Management System, ensuring it remains both effective and compliant.

Your primary focus will revolve around identifying and addressing quality risks, issues, challenges, and opportunities.

Moreover, your responsibilities will extend to:

Leading Regional Quality Projects : You'll spearhead initiatives aimed at ensuring end-to-end quality and compliance for our digital and regional endeavours.

This entails overseeing every aspect of quality assurance and regulatory adherence.


Facilitating Cross-Functional Collaboration :

Working closely with stakeholders and vendors across different departments, you'll orchestrate the planning, coordination, and execution of quality-related activities.

Your ability to foster collaboration will be crucial in maintaining seamless operations.


Implementing a Risk-Based Approach :
Utilizing a proactive and risk-based approach, you'll analyse quality issues and risks, ensuring comprehensive coverage of requirements. Your expertise will be instrumental in devising effective solutions aligned with corporate protocols.


Contributing Innovative Solutions :
Constantly striving for excellence, you'll actively contribute insights and strategies to mitigate quality risks and address emerging issues. Your dedication to delivering best-in-class solutions will drive continuous improvement.

Overseeing Supplier Audits and Management :

As part of your role, you'll take the lead in conducting supplier audits, monitoring their performance, and executing strategic plans to uphold quality standards.

Your meticulous attention to detail will safeguard the integrity of our supply chain.

Qualifications You have decided to apply for this exiting role because you already worked and are familiar with the complexity in affiliates.

You are used to thinking critically and taking responsibility and are looking for a new challenge.

Furthermore, your key qualifications will include:

A master's degree in a relevant subject or a Bachelors' with extensive experience At least 2 years' experience in quality or other GxP area Knowledge of GxP regulations and Quality Management Knowledge and understanding of QMR process.

Ability to work in cross-functional environments. A dynamic and proactive attitude, ability to manage multiple tasks and prioritize workload according to importance. Familiar with various systems, tools and database developed for quality in affiliates.

About the department The Novo Nordisk SEEMEA region is a diverse region of countries and employs more than 4, colleagues who are dedicated in making a remarkable difference to patient care in all the chronic conditions we help to treat.

SEEMEA LECQ is a highly motivated and competent team, responsible for securing quality and compliance in everything we do.

As a member of the SEEMEA LECQ regional team, you will be working closely with regional quality leadership team on securing excellent quality performance, taking a part in various regional projects, and supporting various internal processes ensuring fast product access to patients.

Working at Novo Nordisk At Novo Nordisk, we don't wait for change. We drive it.

We're a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future.

We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them.

From research and development, through to manufacturing, marketing and sales – we're all working to move the needle on patient care.